Department of Oncology, General Hospital, Jinan Command of the People's Liberation Army, Shifan Street 25, Tianqiao District, Jinan 250031, China.
J Cancer Res Clin Oncol. 2012 Jun;138(6):979-89. doi: 10.1007/s00432-012-1171-9. Epub 2012 Feb 23.
P-glycoprotein, the product of the MDR1 gene, is a transmembrane active efflux pump for a variety of environmental toxins and xenobiotics. Epidemiological studies have evaluated the association between MDR1 C3435T polymorphism and cancer susceptibility. However, published data are still inconclusive.
To derive a more precise assessment of this relevance, we performed a meta-analysis, up to September 2010, of 5,196 cases with different cancer types and 6,827 controls from 34 published case-control studies. Summary odds ratios (ORs) and corresponding 95% confidence intervals (CIs) for MDR1 C3435T polymorphism and cancer were estimated using fixed- and random-effects models when appropriate.
The overall results suggested that the variant was associated with a moderately increased cancer risk in all comparison models tested (OR = 1.26, 95% CI: 1.06-1.50 for TT vs. CC; OR = 1.19, 95% CI: 1.04-1.37 for CT vs. CC; OR = 1.15, 95% CI: 1.01-1.32 for recessive model; OR = 1.21, 95% CI: 1.06-1.38 for domain model, and OR = 1.14, 95% CI: 1.04-1.26 for allele contrast). In the subgroup analysis by cancer types, significant associations were found in breast cancer (OR = 1.66, 95% CI: 1.24-2.21 for TT vs. CC; OR = 1.44, 95% CI: 1.14-1.82 for recessive model; OR = 1.41, 95% CI: 1.10-1.81 for domain model; and OR = 1.31, 95% CI: 1.13-1.52 for allele contrast) and renal cancer (OR = 1.99, 95% CI: 1.37-2.90 for TT vs. CC; OR = 1.74, 95% CI: 1.25-2.42 for domain model; OR = 1.43, 95% CI: 1.09-1.88 for recessive model; and OR = 1.40, 95% CI: 1.17-1.68 for allele contrast). However, no significant associations were found in colorectal cancer, gastric cancer, and acute lymphoblastic leukemia for all genetic models. In the ethnicity subgroup analysis, a significant association with cancer among Caucasians was found under the dominant model, homozygote comparison, CT versus CC comparison, and allele comparison.
In summary, this meta-analysis suggests that the MDR1 C3435T polymorphism is associated with cancer susceptibility, increasing the risk of breast and renal cancer.
P-糖蛋白是 MDR1 基因的产物,是一种跨膜主动外排泵,可将多种环境毒素和外源性物质排出细胞。流行病学研究评估了 MDR1 C3435T 多态性与癌症易感性之间的关系。然而,目前已发表的数据仍存在争议。
为了更准确地评估这种相关性,我们对截至 2010 年 9 月的 34 项已发表的病例对照研究中的 5196 例不同癌症类型的病例和 6827 例对照进行了荟萃分析。使用固定效应模型和随机效应模型分别计算 MDR1 C3435T 多态性与癌症的总比值比(OR)及其 95%置信区间(95%CI)。
总体结果表明,在所有测试的比较模型中,变异型与癌症的中度增加风险相关(TT 与 CC 相比,OR=1.26,95%CI:1.06-1.50;CT 与 CC 相比,OR=1.19,95%CI:1.04-1.37;隐性模型,OR=1.15,95%CI:1.01-1.32;域模型,OR=1.21,95%CI:1.06-1.38;等位基因对比,OR=1.14,95%CI:1.04-1.26)。按癌症类型进行亚组分析时,在乳腺癌(TT 与 CC 相比,OR=1.66,95%CI:1.24-2.21;隐性模型,OR=1.44,95%CI:1.14-1.82;域模型,OR=1.41,95%CI:1.10-1.81;等位基因对比,OR=1.31,95%CI:1.13-1.52)和肾癌(TT 与 CC 相比,OR=1.99,95%CI:1.37-2.90;域模型,OR=1.74,95%CI:1.25-2.42;隐性模型,OR=1.43,95%CI:1.09-1.88;等位基因对比,OR=1.40,95%CI:1.17-1.68)中发现与癌症有显著关联,但在结直肠癌、胃癌和急性淋巴细胞白血病中,所有遗传模型均未发现与癌症有显著关联。在种族亚组分析中,显性模型、纯合子比较、CT 与 CC 比较和等位基因比较显示,白种人癌症易感性与 MDR1 C3435T 多态性相关。
综上所述,本荟萃分析表明,MDR1 C3435T 多态性与癌症易感性相关,增加了乳腺癌和肾癌的发病风险。