Department of Science, The Wheatley School, Old Westbury, NY, USA.
J Cancer Res Clin Oncol. 2019 Mar;145(3):625-636. doi: 10.1007/s00432-018-2817-z. Epub 2018 Dec 12.
Mutations in the tumor suppressor gene TP53 are associated with a variety of cancers. Therefore, it is important to know the occurrence and prognostic effects of TP53 mutations in certain cancers.
Over 29,000 cases from the April 2016 release of the International Agency for Research on Cancer (IARC) TP53 Database were analyzed to determine the distribution of germline and somatic mutations in the TP53 gene. Subsequently, 7,893 cancer cases were compiled in cBioPortal for Cancer Genomics from the 33 most recent The Cancer Genome Atlas (TCGA) studies to determine the prevalence of TP53 mutations in cancers and their effects on survival and disease-free survival times.
The data were analyzed, and it was found that the majority of TP53 mutations were missense and the major mutational hotspots were located at codons 248, 273, 175, and 245 in exons 4-8 for somatic mutations with the addition of codon 337 and other mutations in exons 9-10 for germline mutations. Out of 33 TGCA studies, the effects of TP53 mutations were statistically significant in nine cancers (lung adenocarcinoma, hepatocellular carcinoma, head and neck squamous cell carcinoma, acute myeloid leukemia, clear cell renal cell carcinoma (RCC), papillary RCC, chromophobe RCC, uterine endometrial carcinoma, and thymoma) for survival time and in five cancers (pancreatic adenocarcinoma, hepatocellular carcinoma, chromophobe RCC, acute myeloid leukemia, and thymoma) for disease-free survival time. It was also found that the most common p53 mutation in hepatocellular carcinomas (R249S) was a much better indicator for poor prognosis than TP53 mutations as a whole. In addition, in cases of ovarian serous cystadenocarcinoma, the co-occurrence of TP53 and BRCA mutations resulted in longer survival and disease-free survival times than the presence of neither TP53 nor BRCA mutations.
TP53 mutations are potential prognostic markers that can be used to further improve the accuracy of predicting survival and disease-free survival times of cancer patients.
抑癌基因 TP53 的突变与多种癌症有关。因此,了解 TP53 突变在某些癌症中的发生和预后影响非常重要。
分析了国际癌症研究机构(IARC)TP53 数据库 2016 年 4 月发布的超过 29000 例病例,以确定 TP53 基因中外显子 4-8 中胚系和体细胞突变的分布。随后,从 33 项最新的癌症基因组图谱(TCGA)研究中在 cBioPortal for Cancer Genomics 中编译了 7893 例癌症病例,以确定癌症中 TP53 突变的流行率及其对生存和无病生存时间的影响。
对数据进行分析后发现,TP53 突变大多数为错义突变,主要突变热点位于外显子 4-8 的 248、273、175 和 245 密码子,以及外显子 9-10 的 337 密码子和其他突变。在 33 项 TCGA 研究中,TP53 突变对 9 种癌症(肺腺癌、肝细胞癌、头颈部鳞状细胞癌、急性髓系白血病、透明细胞肾细胞癌、乳头状肾细胞癌、嫌色细胞肾细胞癌、子宫内膜癌和胸腺瘤)的生存时间和 5 种癌症(胰腺腺癌、肝细胞癌、嫌色细胞肾细胞癌、急性髓系白血病和胸腺瘤)的无病生存时间有统计学意义。此外,在肝细胞癌中,最常见的 p53 突变(R249S)是比整体 TP53 突变更好的预后指标。此外,在卵巢浆液性囊腺癌病例中,TP53 和 BRCA 突变的同时存在导致生存和无病生存时间长于既没有 TP53 也没有 BRCA 突变的存在。
TP53 突变是潜在的预后标志物,可用于进一步提高预测癌症患者生存和无病生存时间的准确性。