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Mutation of PIK3CA: Possible risk factor for cervical carcinogenesis in older women

机译:PIK3CA突变:老年女性宫颈癌发生的可能危险因素

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PIK3CA encodes the p110α catalytic subunit of PI 3-kinase, which regulates signaling pathways important for neoplasia, cell proliferation and apoptosis. Somatic mutations in this gene have been detected in several solid human tumors. We investigated these mutations in cervical carcinoma and its precursors, and their association with HPV infection and patient clinical data. The mutations were analyzed using post-PCR direct genomic DNA sequencing. Samples included 9 cervical cancer cell lines, 184 invasive cervical carcinomas, and 30 cervical neoplasias. Missense mutations of PIK3CA were identified in 15/184 (8.15%) invasive cervical carcinomas. One novel mutation G1638C (Q546H) was found. Three mutations were identified in the cervical cancer lines. No mutations were found in the precursors. The difference in mutation frequency between invasive and pre-invavasive lesions was not significant (p=0.1372). In relation to age and HPV, the mutation rate was significantly higher in patients ≥60 years (p=0.001), while the rate of HPV infection was higher in patients ≤60 years (p=0.025). No significant correlation with other clinicopathological data was found. The results suggest that PIK3CA mutations are a late event and uncommon in the progression of malignant tumors, but it appears that they facilitate carcinogenesis in older women.
机译:PIK3CA编码PI 3-激酶的p110α催化亚基,它调节对于瘤形成,细胞增殖和凋亡重要的信号通路。已经在几种实体人类肿瘤中检测到了该基因的体细胞突变。我们调查了宫颈癌及其前体中的这些突变,以及它们与HPV感染和患者临床数据的关系。使用PCR后直接基因组DNA测序分析突变。样本包括9种宫颈癌细胞系,184种浸润性宫颈癌和30种宫颈肿瘤。在15/184(8.15%)浸润性宫颈癌中发现了PIK3CA的错义突变。发现了一种新的突变G1638C(Q546H)。在宫颈癌细胞系中鉴定出三个突变。在前体中未发现突变。浸润性和浸润前性病变之间的突变频率差异不明显(p = 0.1372)。关于年龄和HPV,≥60岁的患者的突变率显着更高(p = 0.001),而≤60岁的患者的HPV感染率则更高(p = 0.025)。与其他临床病理数据无显着相关性。结果表明,PIK3CA突变是晚期事件,在恶性肿瘤的进展中并不常见,但似乎它们促进了老年女性的癌变。

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