Chen Huaizeng, Wang Hanzhi, Liu Jia, Cheng Qi, Chen Xiaojing, Ye Feng
Women's Reproductive Health Key Laboratory of Zhejiang Province, Women's Hospital, School of Medicine, Zhejiang University.
Department of Obstetrics and Gynecology, Women's Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, PR China.
Medicine (Baltimore). 2019 Apr;98(17):e15359. doi: 10.1097/MD.0000000000015359.
This study was performed to investigate the relationship between the MUTYH Gln324His (CAG/CAC) genotype and risk of cervical squamous cell carcinoma (CSCC) in a case-control setting. Mismatch amplification-polymerase chain reaction (MA-PCR) was applied to detect the polymorphism in 400 CSCC, 400 CIN III and 1200 control participants. The homozygous His324His (CAC/CAC) genotype of MUTYH was associated with significantly increased risk of CIN III (OR = 1.94) and CSCC (OR = 3.83). Increased risk of CIN III (OR = 1.34) and CSCC (OR = 1.97) was additionally observed with the heterozygous CAG/CAC genotype. Overall, individuals in both CAC/CAC and CAG/CAC genotype groups were at higher risk of cervical carcinoma (CINIII (OR = 1.46) and CSCC (OR = 2.34)). Within the HR-HPV infection-positive group, CAC/CAC and CAG/CAC genotypes were significantly enriched in relation to CIN III and CSCC. Moreover, we observed a positive correlation between the proportion of homozygous CAC/CAC MUTYH genotype and malignant prognostic factors of CSCC, such as cell differentiation grade and lymph node metastasis. These findings clearly highlight associations between the MUTYH Gln324His (CAG/CAC) polymorphism and susceptibility to CSCC, HR-HPV infection and specific prognostic factors, supporting the utility of this variant as an early indicator for patients at high risk of cervical carcinoma.
本研究旨在通过病例对照研究,探讨MUTYH基因Gln324His(CAG/CAC)基因型与宫颈鳞状细胞癌(CSCC)风险之间的关系。采用错配扩增-聚合酶链反应(MA-PCR)检测400例CSCC患者、400例CIN III患者和1200例对照者的基因多态性。MUTYH基因的纯合子His324His(CAC/CAC)基因型与CIN III(OR = 1.94)和CSCC(OR = 3.83)风险显著增加相关。杂合子CAG/CAC基因型也观察到CIN III(OR = 1.34)和CSCC(OR = 1.97)风险增加。总体而言,CAC/CAC和CAG/CAC基因型组个体患宫颈癌(CINIII(OR = 1.46)和CSCC(OR = 2.34))的风险更高。在HR-HPV感染阳性组中,CAC/CAC和CAG/CAC基因型在CIN III和CSCC患者中显著富集。此外,我们观察到纯合子CAC/CAC MUTYH基因型比例与CSCC的恶性预后因素(如细胞分化程度和淋巴结转移)之间呈正相关。这些发现清楚地突出了MUTYH Gln324His(CAG/CAC)多态性与CSCC易感性、HR-HPV感染及特定预后因素之间的关联,支持将该变异作为宫颈癌高危患者的早期指标。