The role of epac in cancer progression

Abstract

Cancer continues to be a prime contributor to global mortality. Despite tremendous research efforts and major advances in cancer therapy, much remains to be learned about the underlying molecular mechanisms of this debilitating disease. A better understanding of the key signaling events driving the malignant phenotype of cancer cells may help identify new pharmaco-targets. Cyclic adenosine 3′,5′-monophosphate (cAMP) modulates a plethora of biological processes, including those that are characteristic of malignant cells. Over the years, most cAMP-mediated actions were attributed to the activity of its effector protein kinase A (PKA). However, studies have revealed an important role for the exchange protein activated by cAMP (Epac) as another effector mediating the actions of cAMP. In cancer, Epac appears to have a dual role in regulating cellular processes that are essential for carcinogenesis. In addition, the development of Epac modulators offered new routes to further explore the role of this cAMP effector and its downstream pathways in cancer. In this review, the potentials of Epac as an attractive target in the fight against cancer are depicted. Additionally, the role of Epac in cancer progression, namely its effect on cancer cell proliferation, migration/metastasis, and apoptosis, with the possible interaction of reactive oxygen species (ROS) in these phenomena, is discussed with emphasis on the underlying mechanisms and pathways. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.

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Keywords

Camp, Cancer, Epac, Pka, Reactive oxygen species (ros), Apoptosis, Cell proliferation, Cyclic amp, Cyclic amp-dependent protein kinases, Disease progression, Guanine nucleotide exchange factors, Humans, Neoplasms, Rap1 gtp-binding proteins, Signal transduction, Agents affecting protein metabolism, Antineoplastic agent, Exchange protein activated by camp, Exchange protein activated by camp modulator, Membrane protein, Polypeptide, Reactive oxygen metabolite, Tumor protein, Unclassified drug, Cyclic amp dependent protein kinase, Guanine nucleotide exchange factor, Rap1 protein, Rapgef3 protein, human, Cancer cell, Cancer growth, Carcinogenesis, Cell migration, Human, Malignant neoplasm, Metastasis, Molecular interaction, Molecularly targeted therapy, Nonhuman, Oxidative stress, Protein function, Protein interaction, Review, Disease exacerbation, Metabolism, Neoplasm, Pathophysiology, Physiology

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