Open Access
Review

The role of astrocytes in brain metastasis at the interface of circulating tumour cells and the blood brain barrier

Layla Burn1,Nicholas Gutowski2,3,Jacqueline Whatmore2,Georgios Giamas1,*,Md Zahidul Islam Pranjol1,*
1
School of Life Sciences, University of Sussex, BN1 9QG Falmer, Brighton, UK
2
College of Medicine and Health, University of Exeter, EX1 2LU Exeter, Devon, UK
3
Royal Devon and Exeter NHS Foundation Trust, EX2 7JU Exeter, Devon, UK
DOI: 10.52586/4969 Volume 26 Issue 9, pp.590-601
Submited: 22 June 2021 Revised: 19 July 2021
Accepted: 04 August 2021 Published: 30 September 2021
(This article belongs to the Special Issue The dynamic roles of glial and stromal cells in neurological diseases)
*Corresponding Author(s):  
Georgios Giamas
E-mail:  
g.giamas@sussex.ac.uk
*Corresponding Author(s):  
Md Zahidul Islam Pranjol
E-mail:  
Z.Pranjol@sussex.ac.uk
Copyright: © 2021 The author(s). Published by BRI. This is an open access article under the CC BY 4.0 license (https://creativecommons.org/licenses/by/4.0/).
Abstract

Tumour metastasis to the brain is a complex process involving crosstalk between the circulating tumour cells and the blood brain barrier (BBB). Astrocytes, which reside in the abluminal surface of the microvasculature of the BBB, are now known to play an essential role in tumour cell migration and invasion into the brain parenchyma. For instance, pro-inflammatory astrocyte secretions, including TNF-α, IL-6, CXCL10 as well as polyunsaturated fatty acids interact with circulating tumour cells to promote migration and proliferation. Additionally, astrocyte and tumour cell derived MMPs play a vital role in tumour cell invasion through the BBB. Understanding these complex interactions between tumour cells and astrocytes in the tumour microenvironment may contribute to the development of novel therapeutics for brain metastasis. Therefore, in this review, we present key interactions within the neurovascular unit of the BBB in the tumour microenvironment that significantly aids cancer metastasis, focusing particularly on astrocytes.

Key words

Astrocytes; Blood brain barrier; Metastasis; Endothelium

2. Introduction

It is estimated that cancer will affect 4 million people in the UK by 2030, an increase from 2.1 million today [1]. Metastasis to the brain involves tumour cells detaching from the primary tumour site by degrading the extracellular matrix (ECM) and entering circulation, followed by arrest and extravasation into a distant organ with the subsequent formation of secondary metastatic lesions [2]. One of the most common type of primary cancer that gives rise to brain metastases is the lung, with nearly 65% of patients estimated to develop this complication [3]. Breast carcinoma and melanoma are other known predominant cases of brain metastasis [4]. Despite brain metastasis being the most common of intracranial tumours, treatment options are limited, with chemotherapy proving clinically ineffective in patients with secondary metastatic brain lesions due to the inability of the drugs to penetrate the BBB [5]. Therefore, brain metastasis has a poor prognosis and is a significant contributor to mortality in patients [6], with the median survival rate ranging from 9 to 15 months [7]. This highlights the urgency to understand the mechanisms underlying tumour cell entry through the BBB and the subsequent rise of secondary lesions. Although rare (3%–5% incidence), brain tumours can metastasise from the brain to other organs, known as extraneural metastases. This can occur through lymphatic drainage, invasion through the dura or bone or invasion through the venous system [8]. However, extraneural metastases is resisted through the lack of ECM proteins in the central nervous system as well as the capillary basement membrane being a physical barrier against metastases migrating into the blood stream [9]. As the severity remains higher for cancer cells metastasising to the brain, this emphasises the need to explore the mechanisms underlying brain metastasis. Although numerous studies have reported the overall extravasation of circulating tumour cells (CTCs) into the brain, the molecular and cellular basis of this mechanism remains largely unknown. Therefore, in this review, we aim to present the current understanding of the molecular interactions and crosstalk between the components of the BBB including endothelial cells, astrocytes and pericytes along with CTCs in the blood-tumour barrier (BTB) that may contribute to the potential development of treatments for this deadly disease.

3. The structure of the blood brain barrier

The BBB is a selective, partially permeable barrier formed of endothelial cells that tightly regulate the transport of ionic and fluid molecules into or from the cerebral microvasculature and brain parenchyma [10]. With tight-junctions and the compact structure of the endothelium, the BBB provides optimal conditions for neuronal function through the regulation of ionic traffic and protection from ionic fluctuations [11]. The fundamental structure of the BBB consists of endothelial cells, astrocytes and pericytes. These form the neurovascular unit (NVU), with endothelial cells being the primary cells of the BBB that interact with the CTCs (Fig. 1) [12].

Figure 1: Structure of the blood brain barrier (BBB), also known as the neurovascular unit, consisting of astrocytic end feet on the abluminal side of the capillary endothelium in close proximity with pericytes also coating the endothelium.

Astrocytes are glial cells in the central nervous system that are essential components of the blood brain barrier [10]. These cells maintain healthy BBB integrity by secreting factors that form and maintain strong tight junctional complexes between endothelial cells [11]. The astrocytes, reside adjacent to the endothelium, with their end feet almost entirely covering the abluminal membrane of the cerebral capillaries [11]. Astrocyte processes at the endothelium form an additional barrier, the glia limitans, by the formation of gap junctions and tight junctions between neighbouring astrocytic projections [13]. The astrocytic end feet tightly connect to the endothelium through specific interactions between the basal lamina and ECM [14]. Pericytes also lie in close contact with the abluminal side and are intimately associated with astrocytic end feet [13]. During development, pericytes coat the endothelial vasculature to produce a basal lamina that promotes accumulation of astrocytic end feet around the endothelium [13]. Due to this intimate relationship, both astrocytes and pericytes in the BBB play vital roles in maintaining barrier integrity and regulating permeability [11].

4. Tumour metastasis and the endothelium

Successful cerebral secondary colonisation requires CTCs to adhere to and transmigrate through the cerebral vascular endothelium, invade the brain parenchyma, proliferate and form secondary lesions [15]. However, not all cancers have the propensity to enter the brain. There is evidence that certain types of cancers such as breast, lung and melanoma are indeed more prone to metastasising to the brain. For instance, patients with Her-2 positive metastatic breast cancer treated with trastuzumab are two-folds more likely to have brain metastasis than other breast cancer types [16]. A similar observation was also found in melanoma patients treated with EGFR kinase inhibitor gefitinib. Interestingly, overexpression of Stat3 in resected human melanoma brain metastases suggested a preferential migratory effect of cancer cells into the brain parenchyma [17]. Stat3 expression also increased angiogenesis and invasion [17]. Interestingly, elevated levels of activated leukocyte cell adhesion molecule (ALCAM) in non-small-cell lung cancer (NSCLC) resulted in an enhanced brain metastasis formation by increased tumour cell dissemination and interaction with BBB endothelium [18].

Additionally, breast cancer cells expressing genes including prostaglandin synthesising enzyme cyclooxygenase-2, MMP1, angiopoietin-like 4 (ANGPTL4), latent TGF-beta1 binding protein (LTBP1), epidermal growth factor receptor (EGFR) ligand HBEGF and fascin-1 were shown to enhance brain metastasis via producing pro-metastatic phenomenon such as inflammation, invasion and cancer cell motility [19]. Moreover, expression of α2,6-sialyltransferase ST6GALNAC5 showed an increased adhesion to brain endothelial cells and thereby, enhanced transmigration of breast cancer cells through the BBB [19].

In a study investigating the role of truncated glioma-associated oncogene homolog 1 (TGLI1) revealed that its high expression results in increased breast cancer metastasis to the brain [20]. TGLI1 resulted in an activation of stemness genes CD44, Nanog, Sox2 and OCT4 in radioresistant cancer stem and metastasis-initiating cells, and through activation of astrocytes, this TGLT1 enhanced brain metastasis [20]. Interestingly, T-cell-induction of Guanylate-Binding Protein 1 expression in oestrogen receptor negative breast cancer cells resulted in preferential seeding to the brain, which could be a novel targeting strategy for immunotherapy [20].

Nevertheless, once at the interface of the BTB, through key interactions, CTCs attach to the endothelium lining, alter the normal physiology of the cerebral vasculature to a pro-tumorigenic state and migrate through the BBB. This metastatic cascade is believed to mirror leukocyte transmigration through the BBB during inflammation [21]. Initial leukocyte rolling and adhesion at the cerebral endothelium is mediated via E-selectin adhesion molecules, followed by activation, arrest, crawling and subsequent migration mediated via intercellular adhesion molecule (ICAM-1) and vascular cell adhesion molecule (VCAM-1) [22]. This raised the possibility that the same adhesion molecules also facilitate and mediate extravasation of CTCs metastasizing to the brain. Previous studies illustrate that direct interactions between tumour cell secretions and the cerebral endothelium facilitates the initial adhesion and arrest of metastatic tumour cells. For instance, Soto et al. [23] demonstrated that the same endothelial adhesion molecules E-selectin, ICAM-1 and VCAM-1 associated with leukocyte trafficking are upregulated on the cerebral endothelium after injection of metastatic breast cancer cells, with the cells overexpressing the natural ligands to the adhesion molecules.

Rai et al. [24] showed that non-small-cell lung carcinoma (NSCLC) cell lines, A549 and SK-MES-1, secrete specific pro-metastatic proteins that directly alter the integrity of the cerebral endothelial glycocalyx. The endothelial glycocalyx is a dense intra-luminal layer lining the healthy cerebral vascular endothelium connected via proteoglycans and glycoproteins forming a mesh network of soluble plasma- and endothelium- derived molecules [25]. The glycocalyx contributes to the maintenance of vascular homeostasis by forming an electrical barrier and regulating vascular permeability [26]. This limits the leakage of macromolecules into the capillaries and regulates adhesion of circulating leukocytes to the cerebral vascular endothelium [27]. Embedded within the glycocalyx are the same adhesion molecules ICAM1, VCAM1 and E-selectin observed in leukocyte extravasation [24]. The A549 and SK-MES-1 cell line secretome consists of inflammatory cytokine tumour necrosis factor-alpha (TNF-α), cathepsin L (CL), cystatin C (CC), vascular endothelial growth factor (VEGF) and insulin-like growth factor binding protein-7 (IGFBP-7). These aid in tumour cell growth and metastasis through increasing endothelial surface E-selectin levels [24]. Moreover, TNF-α induced adhesion of A549 and SK-MES-1 lung cancer cell lines to cerebral endothelial cells by 3.6- and 5.3-folds respectively [24]. In addition, the tumour cell secretome also contains hyaluronidase enzymes that directly degrade the glycocalyx monolayer [28]. Shredding of the glycocalyx coincides with enhanced surface levels of the adhesion molecules E-selectin, ICAM1 and VCAM1 which in turn facilitates rapid adhesion of lung tumour cells to the cerebral endothelium, the first step to metastatic transmigration and cerebral colonisation [24]. Supporting this, Constantinescu et al. [29], observed that degradation of the endothelial glycocalyx in a pro-inflammatory microenvironment also enhances leukocyte immobilization and adhesion at the endothelium. These data suggest that the lung cancer cells secrete factors that directly degrade the cerebral endothelial glycocalyx, exposing embedded adhesion molecules, and thus facilitating their own adhesion and subsequent extravasation across the BBB.

Due to this complex structure and crosstalk within the NVU in the tumour microenvironment, with endothelial cells playing a direct role in metastasis, it is crucial to further understand the specific contributory factors of astrocytic end feet and the astrocyte secretome on BBB physiology and their role in the BTB.

5. Role of Astrocytes in the BBB-CTC interface

During early cerebral colonisation, reactive astrocytes secrete plasminogen activator, an anti-metastatic factor, to inhibit the invading cancer cells [30, 31]). Plasmin induces conversion of membrane-bound astrocytic FasL into an apoptotic signal for cancer cells and inactivation of axon pathfinding molecule L1CAM1 that cancer cells utilise to spread along the brain capillary [31]. Interestingly, these invading cancer cells in the perivascular space secrete serpins to shield this astrocyte-induced defence. However, later on, within the developing cancer microenvironment, astrocytes instead play a pro-tumourigenic role. For instance, earlier studies demonstrate a direct pro-metastatic influence of astrocytes in co-culture with PC14-PE6 lung tumour cells [32], and more recently it has been reported that astrocytes produce and secrete matrix metalloproteinase enzymes -2 and -9 (MMP-2/-9) in the presence of tumour cells that degrade and remodel local ECM, allowing tumour invasion. Moreover, these cells were also shown to induce cancer cell proliferation and chemoprotection by producing pro-inflammatory cytokines IL-6 and TNF-α [33].

More specifically, Wang et al. [34] investigated the hypothesis that astrocyte secretions play a direct role in tumour cell metastasis to the brain. MDA-MB-231 breast cancer cells, sarcoma 180 (S180) cell lines and lung adenocarcinoma (H2030) cells were incubated in astrocytic conditioned media from neonatal rats [34]. The Boyden chamber migration assay showed increased tumour cell migration in response to astrocytic conditioned media (CM), with approximately 200 invading H2030 cells with astrocyte CM compared to 0 for the control without CM, suggesting that factors within the astrocytic secretome play a role in cancer metastasis [34] (Table 1, Ref. [34, 35, 36, 37, 38, 39, 40]). These findings were directly supported by more recent data demonstrating that direct application of astrocytic conditioned medium to MDA-MB-231 metastatic breast cancer cells and MCF10A healthy breast epithelial cells significantly increased invasiveness and velocity of migration of both cell types [41]. Additionally, it was observed that the astrocyte secretome also directly alters morphology of both cell types, forming an elongated and enlarged cellular structure in comparison to control cancer cells without astrocytic conditioned medium [41]. It has been shown that breast cancer cells migrate through the BBB with the adoption of an elongated morphology [4]. This provides a direct link between astrocytes and metastatic cancer cell migration, with the presence of astrocytic secretome facilitating and enhancing tumour cell and healthy epithelial cell migration [41], suggesting this potential is present in the healthy brain. Therefore, astrocytes play a direct role in tumour cell metastasis, perhaps before any potential signalling from tumour cells by increasing transmigration and altering tumour cell morphology of both tumour cells and healthy epithelial cells to a highly favourable phenotype for extravasation and subsequent secondary cerebral colonisation of the brain.

Table 1: Summary of astrocyte secretions in response to trauma/cancer microenvironment aiding the metastatic cascade.
Astrocyte secretion Cell line Function Pathology Reference
MMP-2/-9 and TIMPs NSCLC, H2030, S180, MDA-MB-231 Enzymatic degradation of ECM components, inflammation Cancer, Amyotrophic Lateral Sclerosis (ALS) [34]
CXCL10 sBT-RMS Inflammation and invasion Cancer [35]
TNF-α PBMC, NSCLC, HARA-B Inflammation and proliferation Cancer, Diabetes [36]
Tenascin-C Inflammation and metastasis Cancer, haemorrhage, trauma [37]
Multiple Sclerosis
IFN-α MDA231-BrM2, ErbB2-BrM, H2030-BrM3 Inflammation and proliferation Cancer [38]
IL-6 HARA-B Inflammation and proliferation Cancer [36]
IL-1β HARA-B Inflammation and proliferation Cancer [36]
Polyunsaturated fatty acids BrM (WM4265.2, WM4265.2-BrM1) Pro-metastatic and proliferation Cancer [39]
AEG-1 NSCLC Upregulates release of MMPs Cancer [40]

To investigate the composition of the astrocytic secretome that contributes to the invasiveness of tumour cells, the astrocytic conditioned media was treated with a range of MMP inhibitors [34]. MMP’s are a group of enzymes known to be implicated in cancer metastasis and tumour invasiveness, particularly MMP-2 and MMP-9 that directly degrade collagen and protein components of the ECM and are secreted by both astrocytes and tumour cells [42]. Astrocytes induce the cleavage of inactive pro-MMP-2 and pro-MMP-9 secreted by tumour cells to the active form which degrades collagen IV present in the basement membrane of the BBB, subsequently remodelling the ECM and increasing permeability and enhancing glioma, breast and lung tumour invasiveness to the brain [34]. This is supported by recent studies observing reduced collagen IV in the basement membrane of the BTB within the metastatic cancer microenvironment [43]. Astrocytes indirectly increase the activation of plasmin, a protease, from plasminogen that cleaves and activates tumour cell derived MMPs via interaction with the urokinase plasminogen activator (uPA) [44] (Fig. 2). It has also been shown that reactive astrocytes upregulate MMP secretions specifically within the tumour microenvironment, suggesting a link whereby astrocyte secretions of MMPs in particular, are increased in response to extravasating tumour cell secretions [45], including interleukin-8 (IL-8), plasminogen activator inhibitor-1 (PAI-1) and macrophage migration inhibitory factor (MIF) that activate the astrocytes and induce upregulation of MMPs. In the pathological state, astrocytes are activated and categorised by the upregulated presence of intermediate filament glial fibrillary acidic protein (GFAP) and are termed “reactive astrocytes” [46]. This response to brain insult is known as astrogliosis with astrocytes upregulating GFAP and pro-inflammatory cytokines and chemokines to induce neuroinflammation [37]. The astrocyte culture medium with MMP inhibitors was added to an invasion assay with S180 and H2030 cell lines that resulted in a significant reduction in cancer cell invasion. This was further tested in vivo via the injection of astrocyte-conditioned tumour cells into the left ventricle of the heart in immunodeficient mice to directly enter the circulation to the brain and access the cerebral microenvironment. Astrocyte-conditioned tumour cells demonstrated a more severe tumour metastasis and invaded the brain earlier than astrocyte conditioned tumour cells treated with an MMP inhibitor suggesting a critical role of astrocytes and MMP secretions in the induction of tumour cell transmigration [34]. These findings were supported by recent data demonstrating that inhibition of MMPs within astrocyte culture medium reduced the migratory effects of MDA-MB-231 breast cancer cells in a dose dependent manner [41]. Therefore, astrocytes in the tumour microenvironment not only directly alter morphology and metastatic potential of tumour cells and healthy epithelial cells prior to tumour cell signalling, but also simultaneously secrete MMPs and interact with tumour cell MMP secretions to facilitate extravasation. This suggests that MMP’s are an essential component of astrocytic and tumour cell secretions in the cancer microenvironment that facilitate transmigration.

Astrocytes produce matrix metalloproteinases (MMPs) and induce cleavage of tumour derived MMP-2/MMP-9 via activation of plasmin through interactions with urokinase-type plasminogen activator (UPA). Upregulation of astrocyte elevated gene 1 (AEG-1) enhances release of MMP’s into tumour microenvironment. Uptake of tumour cell derived extracellular vesicles into astrocytes downregulates expression of tissue inhibitors of MMPs (TIMP-2), subsequently diminishing modulation of MMP expression. Astrocyte derived CXCL10 chemokine upregulates the receptor, CXCR3, on CTCs to enhance chemoattraction and migration of tumour cells.

Figure 2: Astrocytes facilitate invasion of circulating tumour cells (CTCs). Astrocytes produce matrix metalloproteinases (MMPs) and induce cleavage of tumour derived MMP-2/MMP-9 via activation of plasmin through interactions with urokinase-type plasminogen activator (UPA). Upregulation of astrocyte elevated gene 1 (AEG-1) enhances release of MMP’s into tumour microenvironment. Uptake of tumour cell derived extracellular vesicles into astrocytes downregulates expression of tissue inhibitors of MMPs (TIMP-2), subsequently diminishing modulation of MMP expression. Astrocyte derived CXCL10 chemokine upregulates the receptor, CXCR3, on CTCs to enhance chemoattraction and migration of tumour cells.

Sun et al. [47] demonstrated that overexpression of astrocyte elevated gene-1 (AEG-1) correlates with high expression and activation of MMP-9. This subsequently enhances tumour invasiveness and metastasis, emphasising the role that astrocytes play in facilitating tumour cell migration. Notably, NSCLC cells engineered to express AEG-1 displayed high levels of MMP-9 correlating to increased invasiveness compared with control [47]. Furthermore, Ding et al. [48] reported that overexpression of AEG-1 also increases lung tumour cell angiogenesis and growth. More recently, Li et al. [40] showed that knockout of AEG-1 inhibited proliferation, migration and invasion of A549 lung cancer cell lines, with overexpression of AEG-1 rescuing this inhibition. This suggests that astrocytes not only secrete MMP’s and cleave pro-MMP’s in the cancer cell secretome, facilitating the degradation of the BBB, but also overexpress AEG-1 which subsequently upregulates MMP-9 expression in the tumour microenvironment and promotes tumour angiogenesis and migration (Fig. 2). Beyond this, Morad et al. [49] demonstrated that extracellular vesicles (EV) derived from metastatic breast cancer cells, following transcytosis across the BBB, can be internalized by surrounding astrocytes via endocytosis. This internalization modulates expression of astrocyte derived MMPs and tissue inhibitors of MMPS (TIMPs) to favour a pro-metastatic tumour microenvironment. Interestingly, metastatic breast cancer EV’s, once internalized by astrocytes, downregulate astrocytic TIMP-2 and in turn reduce inhibition of MMP-2 function on the degradation of the basement membrane of the BBB [49] (Fig. 2). This further highlights a significant role of astrocytes in the facilitation of metastasis, with breast cancer cell EV’s reprogramming astrocytes to reduce modulation of MMP activity through TIMPs. This mechanism along with a strong upregulation of reactive astrocyte derived MMP’s specifically within the cancer microenvironment in response to cancer cell secretions subsequently enhances MMP remodelling of the ECM to create a highly favourable metastatic niche for extravasation. An additional mechanism that promotes brain metastasis through astrocyte-CTC EV crosstalk is the transfer of exosomal microRNAs from astrocytes to CTCs specifically in the cerebral tumour microenvironment. This transfer downregulates PTEN, a vital tumour suppressor, and ultimately promotes tumour cell survival in the brain [50]. This demonstrates both astrocytes and CTC derived EVs enhancing migration as well as diminishing tumour suppression in the brain.

 Tumour cell derived interleukin 8 (IL-8), plasminogen activator inhibitor 1 (PAI-1) and migration inhibitory factor (MIF) activate surrounding astrocytes which subsequently secrete pro-proliferative factors interleukin 6 (IL-6), interleukin 1

Figure 3: Astrocytes facilitate tumour cell proliferation. Tumour cell derived interleukin 8 (IL-8), plasminogen activator inhibitor 1 (PAI-1) and migration inhibitory factor (MIF) activate surrounding astrocytes which subsequently secrete pro-proliferative factors interleukin 6 (IL-6), interleukin 1β (IL-1β) and tumour necrosis factor α (TNF-α). Tumour cells and reactive astrocytes engage in connexin 43 (Cx43) junctions to allow the transfer of cGAMP to astrocytes from the tumour cells. This activates the astrocytic STING pathway intended as a protective immune response with the secretion of TNF-α and interferon-alpha (IFN-α) which activate the pro-proliferative signal transducer and activator of transcription 1 (STAT-1) and NF-kB pathways in tumour cells. Astrocyte derived fatty acid secretions in the tumour microenvironment activate the pro-proliferative peroxisome proliferator-activated receptor gamma (PPARγ) pathway in tumour cells. Tumour cell secretions activate STAT-3 in reactive astrocytes, subsequently reducing immune cell infiltration into the tumour and supporting tumour cell growth and survival.

Therefore, astrocytes play a pivotal role in promoting transmigration of tumour cells across the BBB as well as angiogenesis, growth and survival of tumour cells once they invaded the brain parenchyma. However, Wang et al. [34] observed only a partial inhibition of cancer cell migration with MMP antibodies, suggesting MMP-2/-9 are not the sole factors within the astrocyte secretome aiding cancer cell migration. Despite this, these authors provide evidence for astrocytes facilitating cancer cell migration in metastasis, reacting to and cleaving MMPs from cancer cell secretions and permitting extravasation.

In addition, it is well established that inflammation fosters proliferation and migration of tumour cells, with the tumour microenvironment being predominantly orchestrated by astrocyte-derived inflammatory cytokines [51], which induces the metastatic process. As leukocytes use parallel trans-endothelial migratory mechanisms to metastatic cancer cells, this drives the proposal that astrocytic pro-inflammatory cytokine secretions in response to CTCs may also support and facilitate trans-endothelial migration and ultimate secondary colonisation of tumour cells in the brain [52]. For instance, Doron et al. [35], provided evidence of circulating metastatic melanoma cells hijacking the astrocyte protective inflammatory response to aid in metastasis. CXCL10 is a chemokine secreted by astrocytes in the tumour microenvironment as a protective mechanism during metastasis. However, CTCs exploit this mechanism to their advantage, with upregulation of astrocyte derived CXCL10 in the metastatic environment enhancing tumour cell migration towards astrocytes [35]. The authors observed an upregulation of CXCR3, the CXCL10 receptor, in brain-tropic melanoma cells, with overexpression of CXCR3 in vivo enhancing chemoattraction of melanoma cells and formation of metastases [35] (Fig. 2). This provides further evidence of CTCs directly manipulating astrocytes in the tumour microenvironment to favour and facilitate metastasis.

6. Astrocytes promote cancer cell proliferation

Migration, proliferation and invasion are key steps in tumour growth and metastasis which are dependent on crosstalk between CTCs and the brain microenvironment. Invading tumour cells induce both mechanical (contact inhibition by cadherin and β-catenin dysregulation) and chemical (by secreting cytokines, e.g., IL-8, plasminogen activator inhibitor-1, etc.) disturbances and thus resulting in astrocytic disruption in the brain, leading to astrocytic activation (reviewed in [53]). Since astrocytes are able to induce tumour cell migration, their potential role in cell proliferation has also been investigated. It has been shown that astrocytes localize around metastasising cancer cells and offer a protective role throughout the invasion process and formation of secondary lesions in the brain [52]. To further investigate the potential role of astrocytes in cancer cell proliferation and survival post migration, Seike et al. [36] analysed co-cultures of astrocytes and human lung cancer-derived cells (HARA-B) in mice in vivo. The authors demonstrated that HARA-B cells secrete tumour-cell oriented factors, including IL-8, PAI-1 and MIF, which activate surrounding astrocytes accumulated around the metastatic foci. 4–6 weeks post inoculation of HARA-B cells into the cardiac ventricle in mice, metastatic foci of different sizes were found throughout the brain, with higher accumulation of GFAP-positive astrocytes correlated to larger tumour size; demonstrating a positive relationship between reactive astrocytes and metastatic tumour cells in the tumour microenvironment [36]. These reactive astrocytes subsequently secreted the cytokines interleukin-6 and -1β (IL-6, IL-1β) and TNF-α which induced tumour cell proliferation, with TNF-α mRNA expression in astrocytes being the highest in response to lung tumour cell secretome exposure [36] (Fig. 3). These data suggest that TNF-α is a key component not only for tumour cell adhesion at the endothelium but also for proliferation of tumour cells in the brain. A positive correlation between HARA-B cell and astrocyte ratio and rate of proliferation was observed, with HARA-B cells co-cultured with astrocytes showing a 3-fold increase in proliferation rate compared to either HARA-B cells or astrocytes alone [36]. This demonstrates a mutual relationship between astrocytes and tumour cells to induce and facilitate tumour cell proliferation, with unstimulated astrocytes and tumour cells showing significantly reduced proliferation on their own. Thus, providing direct evidence of astrocyte cytokine secretions in the metastatic microenvironment driving tumour cell proliferation.

Seike et al. [36] went further to investigate whether the mutual relationship between astrocytes and lung cancer cells was specific to the HARA-B cell line. Primary cultured astrocytes were co-cultured with 3 additional cell lines derived from human squamous cell carcinoma (QG56, EBC-1) and NSCLC (PC-9). Proliferation of the additional lung cancer cell lines also significantly increased in the presence of astrocytes, with 350% cell proliferation for HARA-B cells, 200% proliferation for QG56 cells, almost 500% proliferation for EBC-1 cells and 150% proliferation for PC9 cells compared to basal proliferation (100%) without astrocytes [36]. This further supports the notion that astrocytes and tumour cells have a mutual relationship whereby reciprocal stimulation and cross talk promotes proliferation and survival of lung tumour cells in the brain [36]. Furthermore, different concentrations of recombinant mouse cytokines (m), such as mIL-1β, mTNF-α and mIL-6, and neutralizing antibodies were used to confirm the effects of the astrocytic cytokines on lung tumour cell proliferation. These cytokines increased tumour cell proliferation in a dose dependent manner, with 10 pg/mL of mIL-1β increasing tumour cell proliferation by nearly 200% compared with control (no mIL-1β) at 100%, and 500 pg/mL of mTNF-α and mIL-6 increasing proliferation by approximately 150% compared with control with no cytokine at 100%. Additionally, neutralizing antibodies against mIL-1β, mTNF-α and mIL-6 inhibited the growth promoting effect observed in the co-culture, and significantly decreased HARA-B tumour cell proliferation [36]. This provides further direct evidence of a relationship between lung tumour cells and astrocytes, with astrocyte cytokine secretions reacting to and promoting proliferation of tumour cells, placing astrocytes in a critical role in the metastatic process.

In addition, Chen et al. [38] demonstrated that lung carcinoma cells express protocadherin 7 (PCDH7) to engage astrocytes in functional connexin 43 (Cx43) gap junctions. These gap junctions allow lung tumour cells to transfer the second messenger cGAMP to astrocytes which activates the astrocytic immune cGAS-STING pathway. This subsequently results in the release of inflammatory cytokines from reactive astrocytes, including TNF-α and IFN-α, which activate the STAT-1 and NF-kB pathways in CTCs, inducing proliferation and chemoprotection of tumour cells [44] (Fig. 3). Despite STING being an immune response with the role to initially suppress and reject tumour growth, the subsequent astrocytic secretions interact with CTCs and instead promote tumour survival. This cross talk between astrocytes and tumour cells is supported by data demonstrating that gap junctions between tumour cells and astrocytes enable astrocyte-derived cyclic GMP-AMP synthase and microRNAs to be transferred to tumour cells to induce metastasis formation [4]. This supports previous findings and confirms a reciprocal relationship between tumour cells and astrocytes resulting in astrocytic activation and subsequent cytokine secretions which directly facilitate tumour cell growth in the brain [4]. Furthermore, Priego et al. [54], demonstrated that proliferating tumour cells in the brain secrete IL-6, epidermal growth factor (EGF) and transforming growth-factor alpha (TGF-α) that activate the signal transducer and activator of transcription 3 (STAT3) in reactive astrocytes. These astrocytes then reduce the expression of a specific activation marker on CD8+ T cells, subsequently reducing an immune response to the metastatic foci. This creates a barrier of reactive astrocytes around the tumour, reducing access from cytotoxic CD8+ T cells into the core of the tumour and allowing tumour cell growth and survival in the brain [55] (Fig. 3).

Zou et al. [39], showed that metastatic melanoma and breast cancer cell lines in astrocyte culture medium also promoted cancer cell growth. Astrocytes surrounding the metastatic foci in the brain naturally release polyunsaturated fatty acids into the microenvironment to aid in neuronal synaptic formation and function [39]. However, these astrocyte-derived fatty acids are pro-metastatic and activate the peroxisome proliferator-activated receptor γ (PPARγ) signalling pathway in metastatic cancer cells. PPARs are transcription factors activated by ligands, most importantly polyunsaturated fatty acids, that bind to a peroxisome proliferator-activated receptor response element (PPRE) to activate target genes. Subsequently, this PPARγ signalling pathway activation in cancer cells by astrocyte derived fatty acids was observed to be pro-proliferative [39] (Fig. 3). Most importantly, PPARγ antagonism in vivo reversed astrocyte induced proliferation of cancer cells, providing a direct link between increased PPARγ signalling and metastatic growth [39]. This suggests that cancer cells, once migrated across the BBB, exploit the brain microenvironment, specifically the lipid rich environment provided by astrocytes, to proliferate in the brain.

7. Astrocytes in the blood tumour barrier

Within the tumour microenvironment, the blood brain barrier is disrupted and undergoes conformational changes dependent on the progression of metastasis [43]. These physiological changes occur once metastases have been established in the brain and characterise the blood tumour barrier which is highly permeable compared to the healthy BBB [13]. Such changes have been shown to facilitate and aid in the metastatic process by increasing BBB permeability and the ability of cancer cells to extravasate and invade the brain parenchyma [43]. The formation of the BTB involves the accumulation of reactive astrocytes that secrete pro-inflammatory cytokines [13]. Due to the complex interactions within the NVU, astrocytes have the potential to play a key role in cancer extravasation and metastasis within the BTB. For example, aquaporin-4 (AQP-4) is a water channel within the astrocytic end feet that covers the BBB basement membrane and aids in supplying nutrients to surrounding neurons and maintaining vascular homeostasis and ionic regulation in the healthy brain [56]. Additionally, AQP-4 is coexpressed with agrin, a proteoglycan present on the basal lamina, which accumulates around cerebral capillaries for BBB tightening [11]. However, a significant loss of AQP-4 at cerebral vessels at the tumour interface at week 3 post-injection of A549 NSCLC line was observed which persisted throughout the development of mid- and late-stage metastasis, with a 12.18-fold decrease in AQP-4 expression at week 6 [43]. This correlates with the loss of agrin in human brain tumours which could result in an increased permeability of the BBB [57]. Loss of aquaporin-4 has also been observed in breast cancer metastasis to the brain and relates to a loss of polarization of the astrocytic end feet at the BTB contributing to the loss of BBB integrity caused by metastasising cells and favouring their migration [43]. Aquaporins are key regulators of BBB integrity, with studies demonstrating that upregulation of AQP-4 in vivo in gliomas compensates for reduced astrocytic end feet [58]. Furthermore, these findings support observations of decreased levels of AQP-4 in astrocytic end feet in the BTB compared with control, with a reduced and distal distribution of AQP-4 from the end feet at the BTB not localized at the cerebral capillaries [59]. This suggests that not only is AQP-4 expression within astrocytic end feet significantly reduced in the metastatic tumour microenvironment, but that the localization of the end feet is altered and no longer polarized at cerebral blood vessels. AQP-4 reduction is also associated with inflammation [43], potentially induced by pro-inflammatory cytokines in the tumour microenvironment. This suggests that altered astrocyte physiology within the BTB is linked to specific factors released by tumour cells at the metastatic interface and contributes to increased BBB permeability, ultimately aiding the metastatic cascade of cancer cells to the brain.

Furthermore, the absence of astrocytes at the BTB is correlated with down-regulated expression of Mfsd2a, a fatty acid transporter in the cerebral endothelium [60]. In the healthy brain, Mfsd2a mediates transcytosis within endothelial cells, with murine Mfsd2a knockout studies disrupting the cerebral vascular endothelium and increasing transcellular transport and permeability [60]. These findings highlight that astrocyte interactions with the cerebral endothelium are altered in the tumour microenvironment, subsequently degrading BBB integrity and increasing the permeability for cancer cell invasion to the brain parenchyma. Therefore, astrocytes have a significant role in the facilitation of cancer metastasis to the brain, with the tumour microenvironment directly altering astrocyte physiology and displacing astrocytic end feet to enhance entry into the brain.

8. Pericytes and metastasis

To provide a complete picture of the tumour microenvironment at the BTB interface for metastasis, it is essential to include contributions and potential metastatic facilitation from pericytes. Pericytes are multi-functional mural cells that abluminally partially line endothelial cells, coating capillaries and venules throughout the body, with the highest density of pericytes found at cerebral capillaries within the NVU of the BBB [61]. Pericytes are vital in regulating expression of tight junction components and maintaining BBB integrity and vascular tone [62]. Platelet-derived growth factor receptor-β protein (PDGFR-β) within pericytes has a crucial role in modulating homeostasis, vascular tone and integrity of the BBB [43]. Platelet-derived growth factor-β (PDGF-β) is secreted into the basement membrane of the BBB from cerebral endothelial cells, this recruits pericyte coverage of the BBB via their PDGFR-β receptors [59]. Importantly, pericyte-deficient mutant mice displayed significantly increased BBB permeability to different weighted molecular tracers [13], and PDGFR-β knockout mice lacked pericyte populations and had a disrupted BBB [59]. Moreover, overexpression of PDGFR-β increases pericyte accumulation and tumour growth, as well as maintaining vessel integrity [63].

Uzunalli et al. [43] visualised the BTB in immunodeficient mice over 6 weeks using immunofluorescence microscopy after intracardial injection of NSCLC cell lines. At late-stage NSCLC metastasis in week 6, there was a 2.78-fold decrease in PDGFR-β-positive pericytes of the BTB compared to the healthy BBB, with diminished expression of the protein observed from mid-stage metastasis in week 3 onwards [43]. As PDGFR-β knockout studies demonstrate enhanced BBB permeability, this highlights a critical role of pericytes in modulating BBB integrity and vascular transport [64]. Furthermore, a time-dependent increase of desmin expression in pericytes covering the cerebral endothelium was observed in the BTB compared to the BBB with a 3.95-fold increase in desmin positive pericytes in week 5 post intracardial injection of cancer cells [43]. Desmin is a type III intermediate filament protein present in a specific subset of pericytes within the CNS, with overexpression of desmin correlating to increased BBB permeability [59]. These findings highlight significant alterations in pericyte physiology in the tumour microenvironment of metastasis disrupting BBB integrity and vascular tone subsequently facilitating and enhancing tumour cell extravasation into the brain, leading to further tumour cell-astrocyte interaction. Moreover, these findings were supported by previous data displaying significant disruption in PDGFR- β and desmin positive pericyte subpopulations in the BTB of breast cancer brain metastasis [59]. More specifically, Lyle et al. [59] injected breast cancer cell lines into the left ventricle of immunocompromised mice and used uptake of Texas Red dextran as a permeability marker of the BBB. Breast cancer cell metastasis at low BTB permeability was compared with metastasis at high BTB permeability and a significant increase in expression of desmin positive pericytes coverage of the cerebral endothelia was observed associated with high BTB permeability [59]. Therefore, in addition to astrocytes, pericytes also play an important role in the facilitation of extravasation of tumour cells through the BBB.

9. Potential for future studies

It is known that in the cancer microenvironment there is an upregulation of endothelial adhesion molecules for the arrest and subsequent migration of tumour cells across the BBB [24]. However, it is not known whether the astrocyte secretome directly interacts with the endothelium of the BBB during metastasis and upregulates expression of the same adhesion molecules. These events are vital for aiding CTC migration at the BTB interface, and such adhesion molecules provide a potential therapeutic target outside the brain parenchyma. Recent studies provide evidence of potential contributions from astrocytic secretome interacting with the cerebral endothelium and upregulating adhesion molecules for transmigration. For instance, Spampinato et al. [65] demonstrated that the inflammatory cytokine secretions, including TNF-α, from astrocytes enhanced expression of ICAM1 for the transendothelial migration of peripheral blood mononuclear cells (PBMCs). This suggests that astrocytes interact with, and modify endothelial physiology, with reactive astrocyte pro-inflammatory secretions in response to cancer cell secretions enhancing surface levels of an essential endothelial adhesion molecule for extravasation of CTCs into the brain. Incentive is therefore provided to further investigate the potential metastatic facilitation from astrocytes and interactions with endothelial adhesion molecules. An additional hypothesis to investigate involving astrocytes and metastasis is the link between astrocytic tenascin-C within the tumour microenvironment and metastatic tumour cell invasion and proliferation. Tenascin-C (TNC) is an ECM glycoprotein that is downregulated in healthy tissues but overexpressed with GFAP in reactive astrocytes in the pathological brain and is negatively correlated to the presence of AQP-4 in astrocytic end feet [37]. TNC is also highly expressed in the tumour microenvironment of malignant lung, breast and colon cancer [66]. It has been observed that tenascin-C knockout mice are associated with the inhibition of MMP-9 induction and decreased permeability of the BBB, with TNC expression upregulating MMPs in cancer cells [67]. The exact mechanism for this is unknown; however, this provides a link between astrocytes and the BBB. Specifically since TNC expression is associated with cancer cell secretion such as MMPs, it is possible that increased secretions of TNC from astrocytes in the cancer microenvironment may facilitate BBB breakdown in metastasis via MMPs. Additionally, within acute multiple sclerosis plaques, there is a significant loss of TNC, reflecting enzymatic degradation of ECM components and breakdown of the BBB [68]. As with metastasis, astrogliosis is a prominent feature in multiple sclerosis lesions, and this loss of TNC may be via MMPs that directly degrade the ECM and subsequently breakdown the BBB and facilitate leukocyte extravasation (review on astrogliosis [69]). Furthermore, Xia et al. [66] observed that TNC expression promotes invasion of glioblastoma cells, with reduced TNC within the tumour microenvironment inhibiting tumour invasiveness but increasing tumour cell proliferation [66]. These studies demonstrate an influence of TNC expression on tumour cell behaviour correlating to a decrease in AQP-4 in the BTB, with a link between TNC and MMP secretions degrading the BBB for leukocyte and cancer cell extravasation in brain metastases. Currently there are no knockout models which can be used to test this hypothesis with TNC and AQP-4, however these findings provide incentive for further research as to whether targeting TNC could be a potential novel therapeutic in brain metastasis.

Furthermore, patient-derived cancer models are being developed with researchers recently establishing a patient-derived xenograft model system of NSCLC brain metastases [7]. This is being developed with the aim to improve therapeutic approaches to brain metastases. Moreover, further studies are currently being undertaken to investigate potential differential molecular crosstalk in enhancing brain metastasis and therapeutic targets. For instance, in vitro 3D models mimicking the complex BBB microenvironment is currently being developed to closely study the crosstalk between different cell types, barrier function and drug design [70, 71, 72]. Lee et al. [73] have recently developed a microfluidic 3D in vitro system of the BBB by adopting the CNS angiogenesis model. This model successfully showed in vivo-like interactions between pericytes, human brain microvascular endothelial cells and astrocytes, including expressions of tight junctions. Additionally, the authors reported drug penetration via the efflux system that exists in the BBB, a promising step to studying mechanisms of drug delivery in vitro in a CNS model [73]. Moving forward, this model could be developed further to study pathologies by mimicking a damaged BBB to study extravasation of tumour cells into the brain, generating physiological shear pressure which has been shown to regulate vascular permeability and by measuring TEER as another metric of BBB function [74, 75].

10. Conclusions

Within the healthy brain, the neurovascular unit is essential in maintaining vascular endothelial homeostasis, permeability and integrity. However, in the cancer microenvironment, this interface is disrupted, with alterations in astrocyte, pericytes and endothelial properties characterizing the BTB. Circulating tumour cells secrete a complex mix of factors that directly interact with surrounding astrocytes, activating these astrocytes and inducing pro-metastatic secretions that aid in cancer cell adhesion, migration and proliferation. Metastatic tumour cells exploit surrounding astrocytes to facilitate extravasation and survival in the brain, forming a mutual relationship, with reciprocal stimulation being pivotal for tumour growth and survival. Understanding this complex interface of astrocytes, pericytes and cerebral endothelial cells and its manipulation by tumour cells in the tumour microenvironment will provide additional targets for metastatic treatment.

11. Author contributions

LB wrote the majority of the paper. NG and JW partially wrote and critically appraised the paper. GG and MZIP critically revised the paper and supervised the project.

12. Ethics approval and consent to participate

Not applicable.

13. Acknowledgment

Figures were created in Biorender.com.

14. Funding

This research received no external funding.

15. Conflict of interest

The authors declare no conflict of interest.

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Layla Burn, Nicholas Gutowski, Jacqueline Whatmore, Georgios Giamas, Md Zahidul Islam Pranjol. The role of astrocytes in brain metastasis at the interface of circulating tumour cells and the blood brain barrier. Frontiers in Bioscience-Landmark. 2021. 26(9); 590-601.