Bhardwaj Priya, Brown Kristy A
Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Graduate School of Medical Sciences, Weill Cornell Medicine, New York, NY, United States.
Front Oncol. 2021 Mar 30;11:638918. doi: 10.3389/fonc.2021.638918. eCollection 2021.
Obesity is an established risk factor for breast cancer growth and progression. A number of advances have been made in recent years revealing new insights into this link. Early events in breast cancer development involve the neoplastic transformation of breast epithelial cells to cancer cells. In obesity, breast adipose tissue undergoes significant hormonal and inflammatory changes that create a mitogenic microenvironment. Many factors that are produced in obesity have also been shown to promote tumorigenesis. Given that breast epithelial cells are surrounded by adipose tissue, the crosstalk between the adipose compartment and breast epithelial cells is hypothesized to be a significant player in the initiation and progression of breast cancer in individuals with excess adiposity. The present review examines this crosstalk with a focus on obese breast adipose-derived estrogen, inflammatory mediators and adipokines, and how they are mechanistically linked to breast cancer risk and growth through stimulation of oxidative stress, DNA damage, and pro-oncogenic transcriptional programs. Pharmacological and lifestyle strategies targeting these factors and their downstream effects are evaluated for feasibility and efficacy in decreasing the risk of obesity-induced breast epithelial cell transformation and consequently, breast cancer development.
肥胖是乳腺癌生长和进展的既定风险因素。近年来取得了一些进展,揭示了对这种联系的新见解。乳腺癌发展的早期事件涉及乳腺上皮细胞向癌细胞的肿瘤转化。在肥胖状态下,乳腺脂肪组织会发生显著的激素和炎症变化,从而形成有丝分裂原性微环境。肥胖状态下产生的许多因素也已被证明可促进肿瘤发生。鉴于乳腺上皮细胞被脂肪组织包围,脂肪组织区室与乳腺上皮细胞之间的相互作用被认为是肥胖个体乳腺癌发生和进展的重要因素。本综述探讨了这种相互作用,重点关注肥胖乳腺脂肪衍生的雌激素、炎症介质和脂肪因子,以及它们如何通过刺激氧化应激、DNA损伤和促癌转录程序在机制上与乳腺癌风险和生长相关联。针对这些因素及其下游效应的药理学和生活方式策略在降低肥胖诱导的乳腺上皮细胞转化风险以及进而降低乳腺癌发生风险方面的可行性和有效性进行了评估。