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膀胱癌是世界上最常见的恶性肿瘤之一。BCSCs已经被分离但未被定义。我们从膀胱癌组织中分离出BCSCs,从癌旁组织中分离出NBBCs。我们发现,TERT启动子中C228T的突变经常发生在BCSCs,而在NBBCs中不发生。NBBCs中,引入C228T突变会导致TERT过表达和膀胱癌的恶性转化。在BCSCs中,C228T回复突变能够使TERT恢复正常水平并且能够阻止肿瘤的形成。TERT启动子中C228T的突变还能够增加端粒酶的活性。TERT表达水平与膀胱癌的病理分期分级和临床预后显著相关。
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The C228T mutation of TERT promoter frequently occurs in bladder cancer stem cells andcontributes to tumorigenesis of bladder cancer.
Bladder cancer is one of the most common malignant tumors worldwide. Bladder cancer stem cells (BCSCs) have been isolated recently but have not been defined yet. Here we sorted BCSCs from bladder tumor tissues or normalbladder stem cells (NBBCs) from adjacent normal bladder tissues. We found that the C228T mutation (chr5, 1, 295, 228 C > T) of TERT promoter frequently occurs in BCSCs, but not exist in NBBCs. Importantly, introducing the C228Tmutation in NBBCs causes TERT overexpression and transformation of bladder cancer. Restoration of the C228Tmutation to T228C in BCSCs can recover the TERT expression to a basal level and abolish tumor formation. Additionally, the C228T mutation of TERT promoter triggers TERT expression leading to increased telomerase activity.TERT expression levels are consistent with clinical severity and prognosis of bladder cancer.
C228T mutation; bladder cancer stem cells; telomerase reverse transcriptase (TERT); tumorigenesis
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