GJA1-20k, a Short Isoform of Connexin43, from Its Discovery to Its Potential Implication in Cancer Progression

被引:0
|
作者
Fournier, Sarah [1 ]
Clarhaut, Jonathan [2 ,3 ]
Cronier, Laurent [1 ]
Monvoisin, Arnaud [1 ]
机构
[1] Univ Poitiers, Lab Channels & Connexins Canc & Cell Stemness 4CS, UR 22751, 1 Rue Georges Bonnet,TSA 51106, F-86073 Poitiers 09, France
[2] Univ Poitiers, INSERM U1070, Pharmacol Antimicrobial Agents & Antibioresistance, 1 Rue Georges Bonnet TSA 51106, F-86073 Poitiers 09, France
[3] Univ Hosp Ctr Poitiers, 2 Rue Miletrie, F-86021 Poitiers, France
关键词
GJA1-20k; Cx43; trafficking; mitochondria; cancer progression; alternative translation; GAP-JUNCTION PROTEIN; C-TERMINAL DOMAIN; BREAST-CANCER; INTERCELLULAR COMMUNICATION; GLIOMA-CELLS; ALTERNATIVE TRANSLATION; TEMOZOLOMIDE RESISTANCE; MITOCHONDRIAL DYNAMICS; ABERRANT EXPRESSION; OSTEOGENIC NICHE;
D O I
10.3390/cells14030180
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Connexin43 transmembrane protein (Cx43), encoded by the GJA1 gene, is a member of a multigenic family of proteins that oligomerize to form hemichannels and intercellular channels, allowing gap junctional intercellular communication between adjacent cells or communication between the intracellular and extracellular compartments. Cx43 has long been shown to play a significant but complex role in cancer development, acting as a tumor suppressor and/or tumor promoter. The effects of Cx43 are associated with both channel-dependent and -independent functionalities and differ depending on the expression level, subcellular location and the considered stage of cancer progression. Recently, six isoforms of Cx43 have been described and one of them, called GJA1-20k, has also been found to be expressed in cancer cells. This isoform is generated by alternative translation and corresponds to the end part of the fourth transmembrane domain and the entire carboxyl-terminal (CT) domain. Initial studies in the cardiac model implicated GJA1-20k in the trafficking of full-length Cx43 to the plasma membrane, in cytoskeletal dynamics and in mitochondrial fission and subcellular distribution. As these processes are associated with cancer progression, a potential link between Cx43 functions, mitochondrial activity and GJA1-20k expression can be postulated in this context. This review synthetizes the current knowledge on GJA1-20k and its potential involvement in processes related to epithelial-to-mesenchymal transition (EMT) and the proliferation, dissemination and quiescence of cancer cells. Particular emphasis is placed on the putative roles of GJA1-20k in full-length Cx43 exportation to the plasma membrane, mitochondrial activity and functions originally attributed to the CT domain.
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页数:21
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