Department of Microbiology, Immunology, and Cancer Biology, University of Virginia, Charlottesville, Virginia.
Gut Microbes and Health Programme, Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom.
Cancer Immunol Res. 2022 Nov 2;10(11):1309-1325. doi: 10.1158/2326-6066.CIR-21-1120.
Establishing commensal dysbiosis, defined as an inflammatory gut microbiome with low biodiversity, before breast tumor initiation, enhances early dissemination of hormone receptor-positive (HR+) mammary tumor cells. Here, we sought to determine whether cellular changes occurring in normal mammary tissues, before tumor initiation and in response to dysbiosis, enhanced dissemination of HR+ tumors. Commensal dysbiosis increased both the frequency and profibrogenicity of mast cells in normal, non-tumor-bearing mammary tissues, a phenotypic change that persisted after tumor implantation. Pharmacological and adoptive transfer approaches demonstrated that profibrogenic mammary tissue mast cells from dysbiotic animals were sufficient to enhance dissemination of HR+ tumor cells. Using archival HR+ patient samples, we determined that enhanced collagen levels in tumor-adjacent mammary tissue positively correlated with mast cell abundance and HR+ breast cancer recurrence. Together, these data demonstrate that mast cells programmed by commensal dysbiosis activate mammary tissue fibroblasts and orchestrate early dissemination of HR+ breast tumors.
在乳腺癌起始前建立共生失调,定义为具有低生物多样性的炎症性肠道微生物组,可增强激素受体阳性(HR+)乳腺肿瘤细胞的早期扩散。在这里,我们试图确定在肿瘤起始前和对失调的反应中发生在正常乳腺组织中的细胞变化是否增强了 HR+肿瘤的扩散。共生失调增加了正常非肿瘤乳腺组织中肥大细胞的频率和促纤维化性,这种表型变化在肿瘤植入后仍然存在。药理和过继转移方法表明,来自失调动物的促纤维化性乳腺组织肥大细胞足以增强 HR+肿瘤细胞的扩散。使用存档的 HR+患者样本,我们确定肿瘤附近乳腺组织中增强的胶原蛋白水平与肥大细胞丰度和 HR+乳腺癌复发呈正相关。总之,这些数据表明,共生失调编程的肥大细胞激活乳腺组织成纤维细胞,并协调 HR+乳腺癌的早期扩散。