Literature DB >> 25205620

Investigation of cAMP microdomains as a path to novel cancer diagnostics.

Garrett Desman1, Caren Waintraub2, Jonathan H Zippin3.   

Abstract

Understanding of cAMP signaling has greatly improved over the past decade. The advent of live cell imaging techniques and more specific pharmacologic modulators has led to an improved understanding of the intricacies by which cAMP is able to modulate such a wide variety of cellular pathways. It is now appreciated that cAMP is able to activate multiple effector proteins at distinct areas in the cell leading to the activation of very different downstream targets. The investigation of signaling proteins in cancer is a common route to the development of diagnostic tools, prognostic tools, and/or therapeutic targets, and in this review we highlight how investigation of cAMP signaling microdomains driven by the soluble adenylyl cyclase in different cancers has led to the development of a novel cancer biomarker. Antibodies directed against the soluble adenylyl cyclase (sAC) are highly specific markers for melanoma especially for lentigo maligna melanoma and are being described as "second generation" cancer diagnostics, which are diagnostics that determine the 'state' of a cell and not just identify the cell type. Due to the wide presence of cAMP signaling pathways in cancer, we predict that further investigation of both sAC and other cAMP microdomains will lead to additional cancer biomarkers. This article is part of a Special Issue entitled: The role of soluble adenylyl cyclase in health and disease.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cancer; Diagnostics; Microdomain; Soluble adenylyl cyclase; cAMP

Mesh:

Substances:

Year:  2014        PMID: 25205620      PMCID: PMC4281520          DOI: 10.1016/j.bbadis.2014.08.016

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  89 in total

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6.  A nuclear cAMP microdomain suppresses tumor growth by Hippo pathway inactivation.

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8.  MicroRNA-133 Targets Phosphodiesterase 1C in Drosophila and Human Oral Cancer Cells to Regulate Epithelial-Mesenchymal Transition.

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9.  Novel personalized pathway-based metabolomics models reveal key metabolic pathways for breast cancer diagnosis.

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10.  Discovery of LRE1 as a specific and allosteric inhibitor of soluble adenylyl cyclase.

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  10 in total

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