| Literature DB >> 33379194 |
Chang-Xu Chen1,2, Kai-Jun Luo1,2, Jia-Peng Yang3,4, Yun-Chao Huang3,4, Eduardo R Cardenas5, Bruce J Nicholson5, Jean X Jiang5.
Abstract
Connexin-containing gap junctions mediate the direct exchange of small molecules between cells, thus promoting cell-cell communication. Connexins (Cxs) have been widely studied as key tumor-suppressors. However, certain Cx subtypes, such as Cx43 and Cx26, are overexpressed in metastatic tumor lesions. Cyclic adenosine monophosphate (cAMP) signaling regulates Cx expression and function via transcriptional control and phosphorylation. cAMP also passes through gap junction channels between adjacent cells, regulating cell cycle progression, particularly in cancer cell populations. Low levels of cAMP are sufficient to activate key effectors. The present review evaluates the mechanisms underlying Cx regulation by cAMP signaling and the role of gap junctions in cancer progression and metastasis. A deeper understanding of these processes might facilitate the development of novel anticancer drugs.Entities:
Keywords: cAMP; cancer; connexin; metastasis
Year: 2020 PMID: 33379194 PMCID: PMC7795795 DOI: 10.3390/cancers13010058
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639