Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australia.
Cancer Epidemiol Biomarkers Prev. 2022 Dec 5;31(12):2116-2125. doi: 10.1158/1055-9965.EPI-22-0505.
Perturbation of the insulin/insulin-like growth factor (IGF) signaling system is often cited as a mechanism driving breast cancer risk. A systematic review identified prospective cohort studies and Mendelian randomization studies that examined the effects of insulin/IGF signaling (IGF, their binding proteins (IGFBP), and markers of insulin resistance] on breast cancer risk. Meta-analyses generated effect estimates; risk of bias was assessed and the Grading of Recommendations Assessment, Development and Evaluation system applied to evaluate the overall quality of the evidence. Four Mendelian randomization and 19 prospective cohort studies met our inclusion criteria. Meta-analysis of cohort studies confirmed that higher IGF-1 increased risk of breast cancer; this finding was supported by the Mendelian randomization studies. IGFBP-3 did not affect breast cancer. Meta analyses for connecting-peptide and fasting insulin showed small risk increases, but confidence intervals were wide and crossed the null. The quality of evidence obtained ranged from 'very low' to 'moderate'. There were insufficient studies to examine other markers of insulin/IGF signaling. These findings do not strongly support the biological plausibility of the second part of the physical activity-insulin/IGF signaling system-breast cancer pathway. Robust conclusions cannot be drawn due to the dearth of high quality studies. See related article by Swain et al., p. 2106.
胰岛素/胰岛素样生长因子(IGF)信号系统的紊乱通常被认为是导致乳腺癌风险的机制之一。一项系统评价确定了前瞻性队列研究和孟德尔随机化研究,这些研究检查了胰岛素/IGF 信号(IGF、其结合蛋白(IGFBP)和胰岛素抵抗标志物)对乳腺癌风险的影响。荟萃分析生成了效应估计值;评估了偏倚风险,并应用推荐评估、制定和评估系统(Grading of Recommendations Assessment, Development and Evaluation system)对证据的整体质量进行了评估。四项孟德尔随机化研究和 19 项前瞻性队列研究符合我们的纳入标准。队列研究的荟萃分析证实,较高的 IGF-1 增加了乳腺癌的风险;孟德尔随机化研究支持这一发现。IGFBP-3 对乳腺癌没有影响。连接肽和空腹胰岛素的荟萃分析显示出较小的风险增加,但置信区间较宽,且超过了零。获得的证据质量从“非常低”到“中等”不等。没有足够的研究来检查胰岛素/IGF 信号系统的其他标志物。这些发现并不能强有力地支持体力活动-胰岛素/IGF 信号系统-乳腺癌途径的第二部分的生物学合理性。由于高质量研究的缺乏,无法得出明确的结论。请参阅 Swain 等人的相关文章,第 2106 页。