Rat gap junction connexin-30 inhibits proliferation of glioma cell lines

被引:37
作者
Princen, F
Robe, P
Gros, D
Jarry-Guichard, T
Gielen, J
Merville, MP
Bours, V [1 ]
机构
[1] Univ Liege, Lab Med Chem & Med Oncol, B-4000 Liege, Belgium
[2] Univ Liege, Dept Human Physiol, B-4000 Liege, Belgium
[3] Univ Liege, Dept Neurosurg, B-4000 Liege, Belgium
[4] Univ Mediterranee, Lab Genet & Physiol Dev, UMR 6545, Marseille, France
[5] Univ Mediterranee, IBDM, Marseille, France
关键词
D O I
10.1093/carcin/22.3.507
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Connexins, the structural components of gap junctions, control cell growth and differentiation and are believed to belong to a family of tumour suppressor genes. Studies on connexin localization in brain showed that several of these proteins were expressed in distinct compartments of the brain in a cell-type specific manner, indicating that different gap junctions play specific roles in the physiology of the mammalian brain. In this report, we first cloned rat connexin-30 cDNA from brain and showed that it was expressed in long-term primary culture of rat astrocytes, In order to examine the potential role of connexin-30 in tumour cell proliferation, we transfected the connexin-30 cDNA into two rat glioma cell lines (9L and C6) which have lost its expression. Transfected clones adequately expressed membrane-bound connexin-30 protein. Connexin-30-expressing clones showed slower growth, lower DNA synthesis and reduced proliferation in soft agar as compared with the parental and control cells. We concluded that connexin-30 may also probably be considered as a tumour suppressor in rat gliomas.
引用
收藏
页码:507 / 513
页数:7
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