中性粒细胞与携带革兰氏阴性菌的巨噬细胞之间的相互作用会促进肥胖相关性乳腺癌的发生

Sina T. Takle, Sturla Magnus Grondal, Martin E. Lien, Priscilia Lianto, Wei Deng, Reidun Kristine Lillestol, Per Lonning, James B. Lorens, Stian Knappskog, Nils Halberg
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引用次数: 0

摘要

肥胖会促进更具侵袭性的乳腺癌表型。通过对激素受体阴性乳腺癌的空间和单细胞分析,我们发现肥胖患者的肿瘤微环境中富含颗粒酶 B(GZMB)阳性的肿瘤相关中性粒细胞(TANs)亚群。在肥胖环境中演化的乳腺肿瘤中,TANs靠近含有革兰氏阴性细菌脂多糖(LPS)的M2极化巨噬细胞。巨噬细胞的裂解释放出细菌的 LPS,激活局部的 GZMB+ TANs。这会诱导 S100 家族成员 S100A8 的释放,从而促进肿瘤的发展。总之,我们描述了一个由癌细胞、中性粒细胞和 M2 极化巨噬细胞组成的肥胖相关细胞网络,它能促进肿瘤生长。
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Interactions between neutrophils and macrophages harboring gram-negative bacteria promote obesity-associated breast cancer
Obesity promotes a more aggressive breast cancer phenotype. Through spatial and single-cell- based analysis of hormone receptor-negative breast cancers, we identify a subset of tumor- associated neutrophils (TANs) positive for granzyme B (GZMB) enriched in the tumor microenvironment of obese patients. In breast tumors evolved in obese environments, TANs are in proximity of M2 polarized macrophages containing lipopolysaccharides (LPS) from gram- negative bacteria. Pyroptosis of macrophages releases bacterial LPS, activating local GZMB+ TANs. This induces release of the S100 family member S100A8 that promotes tumor progression. In sum, we describe an obesity associated cellular network of cancer cells, neutrophils and M2 polarized macrophages that promotes tumor growth.
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