Chen Wei, Yang Heng, Tang Wen-Ru, Feng Shi-Jun, Wei Yun-Lin
Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, Yunnan, China E-mail :
Asian Pac J Cancer Prev. 2014;15(22):9643-7. doi: 10.7314/apjcp.2014.15.22.9643.
Several studies have been performed to investigate the association of the HER2 Ile655Val polymorphism and breast cancer risk. However, the results were inconsistent. To understand the precise relationship, a meta-analysis was here conducted.
A search of PubMed conducted to investigate links between the HER2 Ile655Val polymorphism and breast cancer, identified a total of 32 studies, of which 29, including 14,926 cases and 15,768 controls, with odds ratios (ORs) with 95% confidence intervals were used to assess any association.
In the overall analysis, the HER2 Ile655Val polymorphism was associated with breast cancer in an additive genetic model (OR=1.136, 95% CI 1.043-1.239, p=0.004) and in a dominant genetic (OR=1.118, 95% CI 1.020-1.227, p=0.018), while no association was found in a recessive genetic model. On subgroup analysis, an association with breast cancer was noted in the additive genetic model (OR=1.111, 95% CI: 1.004-1.230, p=0.042) for the Caucasian subgroup. No significant associations were observed in Asians and Africans in any of the genetic models.
In summary, our meta-analysis findings suggest that the HER2 Ile655Val polymorphism is marginally associated with breast cancer susceptibility in worldwide populations with additive and dominant models, but not a recessive model.
已经进行了多项研究来调查HER2基因Ile655Val多态性与乳腺癌风险之间的关联。然而,结果并不一致。为了明确二者的确切关系,我们进行了一项荟萃分析。
通过检索PubMed来研究HER2基因Ile655Val多态性与乳腺癌之间的联系,共识别出32项研究,其中29项研究(包括14926例病例和15768例对照)的比值比(OR)及其95%置信区间被用于评估二者之间的关联。
在总体分析中,HER2基因Ile655Val多态性在加性遗传模型(OR = 1.136,95% CI 1.043 - 1.239,p = 0.004)和显性遗传模型(OR = 1.118,95% CI 1.020 - 1.227,p = 0.018)中与乳腺癌相关,而在隐性遗传模型中未发现关联。亚组分析显示,在白种人亚组的加性遗传模型中(OR = 1.111,95% CI:1.004 - 1.230,p = 0.042)该多态性与乳腺癌有关。在任何遗传模型中,亚洲人和非洲人未观察到显著关联。
总之,我们的荟萃分析结果表明,HER2基因Ile655Val多态性在全球人群中,与乳腺癌易感性在加性和显性模型中存在微弱关联,但与隐性模型无关。