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Insights into exchange factor directly activated by cAMP (EPAC) as potential target for cancer treatment

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Abstract

Cancer remains a global health problem and approximately 1.7 million new cancer cases are diagnosed every year worldwide. Although diverse molecules are currently being explored as targets for cancer therapy the tumor treatment and therapy is highly tricky. Secondary messengers are important for hormone-mediated signaling pathway. Cyclic AMP (cAMP), a secondary messenger responsible for various physiological processes regulates cell metabolism by activating Protein kinase A (PKA) and by targeting exchange protein directly activated by cAMP (EPAC). EPAC is present in two isoforms EPAC1 and EPAC2, which exhibit different tissue distribution and is involved in GDP/GTP exchange along with activating Rap1- and Rap2-mediated signaling pathways. EPAC is also known for its dual role in cancer as pro- and anti-proliferative in addition to metastasis. Results after perturbing EPAC activity suggests its involvement in cancer cell migration, proliferation, and cytoskeleton remodeling which makes it a potential therapeutic target for cancer treatments.

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Acknowledgements

Seema Sehrawat is the recipient of Bio-CARe Award from Ministry of Science and Technology, Department of Biotechnology, Govt. of India, and acknowledges the funding support. Aaron Goldman is supported by the Breast Cancer Alliance Young Investigator Award, USA. Shiv Nadar Foundation is acknowledged for providing the PhD fellowship to Mr. Naveen Kumar and Mr. Peeyush Prasad. The funding agency had no role in design of the study, collection and analysis of the data, decision to publish, or manuscript preparation.

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Correspondence to Aaron Goldman or Seema Sehrawat.

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AG is an employee of Mitra Biotech and holds equity. All other authors declare no conflict of interest.

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Kumar, N., Prasad, P., Jash, E. et al. Insights into exchange factor directly activated by cAMP (EPAC) as potential target for cancer treatment. Mol Cell Biochem 447, 77–92 (2018). https://doi.org/10.1007/s11010-018-3294-z

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  • DOI: https://doi.org/10.1007/s11010-018-3294-z

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