Zhang Guangzhe, Xu Qian, Liu Jingwei, Lv Zhi, Lu Youzhu, Yang Huaiwei, Sun Liping, Xing Chengzhong, Yuan Yuan
Tumor Etiology and Screening Department of Cancer Institute and General Surgery, the First Hospital of China Medical University, and Key Laboratory of Cancer Etiology and Prevention (China Medical University), Liaoning Provincial Education Department, Shenyang 110001, China.
J Cancer. 2019 Apr 20;10(7):1772-1780. doi: 10.7150/jca.26722. eCollection 2019.
Although the impact and potential mechanisms of p53 polymorphisms on human malignancies have been intensively studied, analyses for association between p53 polymorphisms and colorectal cancer (CRC) risk were still limited to some common variants. Moreover, the majority of previous studies did not classify the specimens of CRC based on tumor location. This case-control study aimed to evaluate the association of five p53 polymorphisms (rs1042522, rs12947788, rs1625895, rs2909430 and rs12951053) with the risk of low rectal cancer (LRC) and investigate the prognostic significance. A total of 347 cases and 353 controls from a Chinese population were recruited and genotyped using KASP assay. Individuals carrying the variant rs12947788 A allele were observed to associate with an increased risk of LRC. After stratification for clinicopathological parameters, rs12947788 was significantly co-related with the histological type of LRC under a dominant model. Although none of the selected p53 polymorphisms was significantly associated with patient prognosis in total population, significant associations with the overall survival were revealed in the heterozygosis carriers vs. wild type carriers model through subgroup analyses based on clinical characteristics. Moreover, haplotype analyses showed that C-A-G-A-A haplotype was associated with a significantly higher LRC risk as compared to the other haplotypes. In low rectal cancer, P53 protein expression was obviously higher in p53 rs1042522 mutant carriers than in other genotypes. Our study further proves the involvement of p53 polymorphisms in pathogenesis of LRC and may provide potential therapeutic implications.
尽管p53基因多态性对人类恶性肿瘤的影响及潜在机制已得到深入研究,但p53基因多态性与结直肠癌(CRC)风险之间关联的分析仍局限于一些常见变异。此外,以往大多数研究并未根据肿瘤位置对CRC标本进行分类。本病例对照研究旨在评估5种p53基因多态性(rs1042522、rs12947788、rs1625895、rs2909430和rs12951053)与低位直肠癌(LRC)风险的关联,并探讨其预后意义。共招募了347例病例和353例来自中国人群的对照,并使用竞争性等位基因特异性PCR(KASP)分析进行基因分型。观察到携带rs12947788变异A等位基因的个体与LRC风险增加相关。在对临床病理参数进行分层后,在显性模型下,rs12947788与LRC的组织学类型显著相关。尽管所选的p53基因多态性在总体人群中均未与患者预后显著相关,但通过基于临床特征的亚组分析,在杂合子携带者与野生型携带者模型中发现了与总生存期的显著关联。此外,单倍型分析表明,与其他单倍型相比,C-A-G-A-A单倍型与LRC风险显著更高相关。在低位直肠癌中,p53 rs1042522突变携带者的P53蛋白表达明显高于其他基因型。我们的研究进一步证明了p53基因多态性参与低位直肠癌的发病机制,并可能提供潜在的治疗意义。