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磷脂酰肌醇-3激酶催化亚基α(PIK3CA)突变:老年女性宫颈癌发生的可能危险因素。

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

作者信息

Cui Baoxia, Zheng Biying, Zhang Xi, Stendahl Ulf, Andersson Sonia, Wallin Keng-Ling

机构信息

Department of Molecular Medicine and Surgery, Karolinska University Hospital Solna, Karolinska Institutet, Stockholm, Sweden.

出版信息

Int J Oncol. 2009 Feb;34(2):409-16.

Abstract

PIK3CA encodes the p110alpha 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-invasive lesions was not significant (p=0.1372). In relation to age and HPV, the mutation rate was significantly higher in patients>or=60 years (p=0.001), while the rate of HPV infection was higher in patients<or=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.

摘要

PIK3CA基因编码磷脂酰肌醇3激酶的p110α催化亚基,该亚基调节对肿瘤形成、细胞增殖和凋亡至关重要的信号通路。在几种人类实体瘤中已检测到该基因的体细胞突变。我们研究了宫颈癌及其癌前病变中的这些突变,以及它们与HPV感染和患者临床数据的关联。采用PCR后直接基因组DNA测序分析这些突变。样本包括9个宫颈癌细胞系、184例浸润性宫颈癌和30例宫颈肿瘤。在184例浸润性宫颈癌中有15例(8.15%)检测到PIK3CA的错义突变。发现了一个新的突变G1638C(Q546H)。在宫颈癌细胞系中鉴定出3个突变。在癌前病变中未发现突变。浸润性和浸润前病变之间的突变频率差异无统计学意义(p = 0.1372)。关于年龄和HPV,年龄≥60岁的患者突变率显著更高(p = 0.001),而年龄≤60岁的患者HPV感染率更高(p = 0.025)。未发现与其他临床病理数据有显著相关性。结果表明,PIK3CA突变是恶性肿瘤进展中的晚期事件且不常见,但似乎它们促进老年女性的致癌作用。

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