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胆囊收缩素(CCK)和胆囊收缩素受体(CCKAR)基因变异与胆道癌和结石易感性的关系:中国上海的一项基于人群的研究。

Variants in CCK and CCKAR genes to susceptibility to biliary tract cancers and stones: a population-based study in Shanghai, China.

机构信息

Department of Epidemiology, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine.

出版信息

J Gastroenterol Hepatol. 2013 Sep;28(9):1476-81. doi: 10.1111/jgh.12278.

Abstract

BACKGROUND AND AIM

Altered motility of the gallbladder is associated with an increased risk of gallstones and can result in biliary tract cancers. Cholecystokinin (CCK) is an important modulator of gallbladder motility which functions by activating CCK type-A receptor (CCKAR). The aim of this study was to determine whether genetic variants in CCK and CCKAR are associated with the risk of biliary tract cancers and stones.

METHODS

We investigated the associations between nine single nucleotide polymorphisms in CCK and CCKAR in a population-based case-control study, including 439 biliary tract cancer cases (253 gallbladder, 133 extrahepatic bile duct, and 53 ampulla of Vater cancer cases), 429 biliary stone cases, and 447 population controls in Shanghai, China.

RESULTS

We found that women with the CCKAR rs1800855 AA genotype had an increased risk of gallbladder cancer (odds ratio = 2.37, 95% confidence interval (CI): 1.36-4.14) compared with subjects with the TT genotype, and remained significant after Bonferroni correction (P = 0.0056). Additionally, female carriers of the CCKAR haplotype C-T-C-T (rs2071011-rs915889-rs3822222-rs1800855) had a reduced risk of gallbladder cancer (odds ratio = 0.61, 95% confidence interval: 0.43-0.86) compared with those with the G-C-C-A haplotype; the association also remained significant after Bonferroni correction.

CONCLUSIONS

These findings suggest that variants in the CCKAR gene may influence the risk of gallbladder cancer in women. Additional studies are needed to confirm our findings.

摘要

背景与目的

胆囊运动功能的改变与胆结石风险的增加有关,并可能导致胆道癌。胆囊收缩素(CCK)是调节胆囊运动的重要调节剂,通过激活胆囊收缩素 A 型受体(CCKAR)发挥作用。本研究旨在确定 CCK 和 CCKAR 中的遗传变异是否与胆道癌和结石的风险相关。

方法

我们在中国上海进行了一项基于人群的病例对照研究,包括 439 例胆道癌病例(253 例胆囊癌、133 例肝外胆管癌和 53 例壶腹癌)、429 例胆石症病例和 447 例人群对照,研究了 CCK 和 CCKAR 中 9 个单核苷酸多态性与胆道癌和结石风险的关系。

结果

我们发现,与 TT 基因型相比,女性 CCKAR rs1800855 AA 基因型的胆囊癌风险增加(比值比=2.37,95%置信区间:1.36-4.14),且在 Bonferroni 校正后仍有统计学意义(P=0.0056)。此外,与携带 G-C-C-A 单倍型的个体相比,女性 CCKAR 单倍型 C-T-C-T(rs2071011-rs915889-rs3822222-rs1800855)的携带者患胆囊癌的风险降低(比值比=0.61,95%置信区间:0.43-0.86);在 Bonferroni 校正后,该关联仍然显著。

结论

这些发现表明 CCKAR 基因中的变异可能影响女性胆囊癌的风险。需要进一步的研究来证实我们的发现。

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