Open Access

Integrating leptin and cAMP pathways in triple-negative breast cancer cells

Annamaria Spina1,Francesca Di Maiolo1,Antonietta Esposito1,Raffaella D’Auria1,Davide Di Gesto1,Emilio Chiosi1,Luca Sorvillo1,Silvio Naviglio1,*
Department of Biochemistry and Biophysics, Second University of Naples, Medical School, Via L. De Crecchio 7, 80138 Naples, Italy
DOI: 10.2741/4092 Volume 18 Issue 1, pp.133-144
Published: 01 January 2013
(This article belongs to the Special Issue BRCA1 and BRCA2 role in cancer)
*Corresponding Author(s):  
Silvio Naviglio

Triple-negative breast cancers are characterised by an aggressive phenotype, are often found in younger women and have been associated with poor prognosis. Because triple-negative breast cancer patients are unresponsive to current targeted therapies and other treatment options are only partially effective, new pharmacological approaches are warranted. The obesitylinked adipokine, leptin, is a well known mitogen/survival factor in breast cancer cells and several studies have addressed its role in breast cancer. Surprisingly, recent in vitro studies have shown that leptin enhances the anti- proliferative effects of cAMP elevation in triple-negative breast cancer cells by apoptosis induction. In the current review, we discuss on the role of cAMP as a growth suppressor and of leptin as a growth promoting factor in breast cancer cells and we will focus on the molecular pathways involved in the antiproliferative interaction between leptin and cAMP elevation. The rationale for the possible development of a simple, cheap and innovative approach for therapeutic intervention in triple-negative breast cancer, based on the use of cAMP elevating drugs at tolerable doses, will be discussed.

Key words

Breast Cancer, STAT3, Novel Anticancer Therapy, cAMP elevating agents, SOCS3

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Annamaria Spina, Francesca Di Maiolo, Antonietta Esposito, Raffaella D’Auria, Davide Di Gesto, Emilio Chiosi, Luca Sorvillo, Silvio Naviglio. Integrating leptin and cAMP pathways in triple-negative breast cancer cells. Frontiers in Bioscience-Landmark. 2013. 18(1); 133-144.