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首页> 外文期刊>Nature Communications >TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
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TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling

机译:TSPAN8通过激活Sonic Hedgehog信号传导促进癌细胞茎

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Cancer stem cells (CSCs) represent a major source of treatment resistance and tumor progression. However, regulation of CSCs stemness is not entirely understood. Here, we report that TSPAN8 expression is upregulated in breast CSCs, promotes the expression of the stemness gene NANOG, OCT4, and ALDHA1, and correlates with therapeutic resistance. Mechanistically, TSPAN8 interacts with PTCH1 and inhibits the degradation of the SHH/PTCH1 complex through recruitment of deubiquitinating enzyme ATXN3. This results in the translocation of SMO to cilia, downstream gene expression, resistance of CSCs to chemotherapeutic agents, and enhances tumor formation in mice. Accordingly, expression levels of TSPAN8, PTCH1, SHH, and ATXN3 are positively correlated in human breast cancer specimens, and high TSPAN8 and ATXN3 expression levels correlate with poor prognosis. These findings reveal a molecular basis of TSPAN8-enhanced Sonic Hedgehog signaling and highlight a role for TSPAN8 in promoting cancer stemness.
机译:癌症干细胞(CSCs)代表治疗抗性和肿瘤进展的主要来源。然而,不完全理解CSCS茎的调节。这里,我们认为TSPAn8表达在乳腺CSC中上调,促进茎秆基因纳米,Oct4和Aldha1的表达,并与治疗性相关。机械地,TSPAN8与PTCH1相互作用,并通过募集脱硫酶ATOxN3来抑制SHH / PTCH1复合物的降解。这导致将SMO转化为纤毛,下游基因表达,CSCs对化学治疗剂的抗性,并增强小鼠中的肿瘤形成。因此,TSPAn8,PTCH1,SHH和ATXN3的表达水平在人乳腺癌标本中呈正相关,高TSPAN8和ATXN3表达水平与预后差相关。这些发现揭示了Tspan8增强的Sonic Hedgehog信号传导的分子基础,并突出了Tspan8在促进癌症茎中的作用。

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