Authors' Affiliations: Developmental, Molecular, and Chemical Biology Department, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine; Molecular Oncology Research Institute and Medical Oncology and Department of Pathology, Tufts Medical Center, Boston, Massachusetts; and Departments of Medicine, Duke University, Durham, North Carolina.
Cancer Res. 2013 Oct 1;73(19):6080-93. doi: 10.1158/0008-5472.CAN-13-0926. Epub 2013 Aug 19.
Obesity is one of the most important preventable causes of cancer and the most significant risk factor for breast cancer in postmenopausal women. Compared with lean women, obese women are more likely to be diagnosed with a larger, higher grade tumor, an increased incidence of lymph node metastases, and elevated risk of distant recurrence. However, the mechanisms connecting obesity to the pathogenesis of breast cancer are poorly defined. Here, we show that during obesity, adipocytes within human and mouse breast tissues recruit and activate macrophages through a previously uncharacterized CCL2/IL-1β/CXCL12 signaling pathway. Activated macrophages in turn promote stromal vascularization and angiogenesis even before the formation of cancer. Recapitulating these changes using a novel humanized breast cancer model was sufficient to promote angiogenesis and prime the microenvironment prior to neoplastic transformation for accelerated breast oncogenesis. These findings provide a mechanistic role for adipocytes and macrophages before carcinogenesis that may be critical for prevention and treatment of obesity-related cancer.
肥胖是癌症最重要的可预防病因之一,也是绝经后妇女乳腺癌的最重要危险因素。与瘦女性相比,肥胖女性更有可能被诊断出患有更大、更高分级的肿瘤,淋巴结转移的发生率更高,远处复发的风险也更高。然而,将肥胖与乳腺癌发病机制联系起来的机制尚未明确。在这里,我们表明,在肥胖期间,人乳腺组织和小鼠乳腺组织中的脂肪细胞通过一种以前未被描述的 CCL2/IL-1β/CXCL12 信号通路招募和激活巨噬细胞。活化的巨噬细胞反过来促进基质血管生成和血管生成,甚至在癌症形成之前。使用新的人源化乳腺癌模型再现这些变化足以促进血管生成,并在肿瘤转化前为微环境做好准备,从而加速乳腺癌的发生。这些发现为致癌前脂肪细胞和巨噬细胞提供了一个潜在的作用机制,这可能对预防和治疗肥胖相关癌症至关重要。