高GLP1R基因拷贝数与多种癌症的微卫星不稳定性和胶质母细胞瘤的更好生存概率相关。

IF 3.4 3区 生物学 Q3 CELL BIOLOGY
Teresa M Thomas, Michael T Aboujaoude, Vayda R Barker, Mallika Varkhedi, Rahul Jain, George Blanck
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引用次数: 0

摘要

虽然Warburg效应是众所周知的,并且经常被研究,但促进肿瘤细胞糖酵解活性增加的分子特征尚未被广泛研究。我们假设,与糖代谢相关的蛋白质编码基因的扩增可能是促进糖酵解增加的机制。因此,我们对三种不同癌症类型的GLP1R、AMFR、GCG、GPI和ACTA1基因应用了精确指导的拷贝数变异分析方法。结果表明,胶质母细胞瘤中GLP1R的高CNs与较好的患者预后相关,而低级别胶质瘤中GPI的高CNs与较差的患者预后相关。结果还表明,高微卫星不稳定性与上述大多数基因的高CNs直接相关。这些评估肿瘤代谢相关基因的方法可能导致更准确的患者风险测量和潜在的额外治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High GLP1R gene copy numbers associated with microsatellite instability for multiple cancers and with better survival probabilities for glioblastoma.

While the Warburg effect is well-known and frequently studied, the molecular features that facilitate increased tumor cell glycolytic activity have yet to be extensively investigated. We hypothesized that amplification of genes encoding proteins related to glucose metabolism could be a mechanism to facilitate increased glycolysis. Thus, we applied a precision-guided copy number variation analysis approach to the GLP1R, AMFR, GCG, GPI, and ACTA1 genes across three different cancer types. Results indicated that higher CNs of GLP1R in glioblastoma were associated with better patient outcomes, while high CNs of GPI in lower-grade gliomas were associated with worse outcomes. Results also indicated that high microsatellite instability directly correlated with high CNs for most of the above indicated genes. These approaches to assessing tumor metabolism-related genes may lead to more accurate measures of patient risk and potential additional treatment options.

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来源期刊
Cell Cycle
Cell Cycle 生物-细胞生物学
CiteScore
7.70
自引率
2.30%
发文量
281
审稿时长
1 months
期刊介绍: Cell Cycle is a bi-weekly peer-reviewed journal of high priority research from all areas of cell biology. Cell Cycle covers all topics from yeast to man, from DNA to function, from development to aging, from stem cells to cell senescence, from metabolism to cell death, from cancer to neurobiology, from molecular biology to therapeutics. Our goal is fast publication of outstanding research.
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