Department of Microbiology and Immunology, University of Louisville, 505 South Hancock Street, Louisville, KY 40202, USA.
Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, KY, USA.
Cell Metab. 2018 Nov 6;28(5):689-705.e5. doi: 10.1016/j.cmet.2018.07.006. Epub 2018 Aug 9.
It is clear that obesity increases the risk of many types of cancer, including breast cancer. However, the underlying molecular mechanisms by which obesity is linked to cancer risk remain to be defined. Herein, we report that circulating adipose fatty acid binding protein (A-FABP) promotes obesity-associated breast cancer development. Using clinical samples, we demonstrated that circulating A-FABP levels were significantly increased in obese patients with breast cancer in comparison with those without breast cancer. Circulating A-FABP released by adipose tissue directly targeted mammary tumor cells, enhancing tumor stemness and aggressiveness through activation of the IL-6/STAT3/ALDH1 pathway. Importantly, genetic deletion of A-FABP successfully reduced tumor ALHD1 activation and obesity-associated mammary tumor growth and development in different mouse models. Collectively, these data suggest circulating A-FABP as a new link between obesity and breast cancer risk, thereby revealing A-FABP as a potential new therapeutic target for treatment of obesity-associated cancers.
很明显,肥胖会增加多种癌症的风险,包括乳腺癌。然而,肥胖与癌症风险相关的潜在分子机制仍有待确定。在此,我们报告循环脂肪组织脂肪酸结合蛋白(A-FABP)可促进肥胖相关的乳腺癌发生。通过临床样本,我们发现与无乳腺癌的患者相比,肥胖伴乳腺癌患者的循环 A-FABP 水平显著升高。脂肪组织释放的循环 A-FABP 可直接靶向乳腺肿瘤细胞,通过激活 IL-6/STAT3/ALDH1 通路增强肿瘤干性和侵袭性。重要的是,A-FABP 的基因缺失成功减少了肿瘤 ALDH1 的激活以及不同小鼠模型中肥胖相关的乳腺肿瘤生长和发展。总的来说,这些数据表明循环 A-FABP 是肥胖和乳腺癌风险之间的新联系,从而揭示 A-FABP 是治疗肥胖相关癌症的潜在新治疗靶点。