癌症驱动基因的突变:对前列腺癌进展的洞察

S. Prasad, S. Srivastava
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引用次数: 0

摘要

前列腺癌是男性最常见的泌尿肿瘤疾病之一,也是全球男性癌症相关死亡的主要原因。体细胞突变与癌症的发生有着密切的联系。癌基因和肿瘤抑制基因的突变改变了关键的细胞功能,可导致前列腺癌的发生和发展。全基因组测序已经确定了许多遗传变异,并进一步提供了驱动前列腺癌进展的基因突变的详细视图。TP53、SPOP、PTEN、ATM、AR、CTNNB1、FOXA1、KMT2D、BRACA2和APC是前列腺癌中常见的突变基因。本综述利用来自cBioPortal和PubMed的数据,总结了这些驱动基因突变对前列腺癌生存、进展和转移的现状和可能的影响。这项研究将有助于更好地了解前列腺癌患者临床变异性的生物学基础,并可能提供新的遗传诊断标记和药物靶点。
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Mutations in Cancer Driver Genes: An Insight into Prostate Cancer Progression
Prostate cancer is one of the most common uro-oncological disease in men and is globally leading cause of cancer related deaths in males. The somatic mutation has a strong link in the occurrence of cancer. Mutation in the oncogenes and tumor suppressor genes that alter key cellular functions can lead to prostate cancer initiation and progression. Whole genome sequencing has identified numerous genetic alternations and further provided a detail view of the mutations in genes that drive progression of prostate cancer. TP53, SPOP, PTEN, ATM, AR, CTNNB1, FOXA1, KMT2D, BRACA2 and APC were found as frequently mutated genes in prostate cancer. Using data from cBioPortal and PubMed, this review summarizes the status and possible impact of mutations in these driver genes on survival, progression, and metastasis of prostate cancer. This study will contribute a better understanding of biological basis for clinical variability in prostate cancer patients and may provide new genetic diagnostic markers and drug targets.
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