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Genes and pathways downstream of telomerase in melanoma metastasis

机译:黑色素瘤转移中端粒酶下游的基因和途径

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Recent studies have demonstrated a role for telomerase in driving tumor progression, but its mechanism of action remains unclear. Here we show that stable, ribozyme-mediated suppression of mouse telomerase RNA reduced telomerase RNA expression, telomerase activity, and telomere length, which significantly reduced tumor invasion and metastatic potential. Our studies reveal that previously unidentified effects of telomerase may mediate its tumor-promoting effects. First, reducing telomerase activity induced a more dendritic morphology, accompanied by increased melanin content and increased expression of tyrosinase, a key enzyme in melanin biosynthesis. Second, gene expression profiling revealed that telomerase targeting down-regulated expression of several glycolytic pathway genes, with a corresponding decrease in glucose consumption and lactate production. Thus, telomerase activity controls the glycolytic pathway, potentially altering the energy state of tumor cells and thereby modulating tyrosinase activity and melanin production. These studies have important implications for understanding the mechanisms by which telomerase promotes tumor invasion and metastasis.
机译:最近的研究表明端粒酶在驱动肿瘤进展中的作用,但其作用机理仍不清楚。在这里,我们显示稳定,核酶介导的小鼠端粒酶RNA的抑制降低了端粒酶RNA的表达,端粒酶活性和端粒长度,从而显着降低了肿瘤的侵袭和转移潜力。我们的研究表明,端粒酶以前无法确定的作用可能介导了其促肿瘤作用。首先,端粒酶活性降低导致树突状形态增加,同时黑色素含量增加和酪氨酸酶表达增加,酪氨酸酶是黑色素生物合成中的关键酶。第二,基因表达谱分析表明端粒酶靶向下调了几种糖酵解途径基因的表达,相应地减少了葡萄糖的消耗和乳酸的产生。因此,端粒酶活性控制糖酵解途径,潜在地改变肿瘤细胞的能量状态,从而调节酪氨酸酶活性和黑色素的产生。这些研究对于理解端粒酶促进肿瘤侵袭和转移的机制具有重要意义。

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