Suppr超能文献

脂肪细胞特异性Zeb1下调重塑肿瘤相关脂肪微环境以促进女性乳腺癌进展。

Adipocyte-specific Zeb1 downregulation remodels the tumor-associated adipose microenvironment to facilitate female breast cancer progression.

作者信息

Cao Lixia, Sun Wei, Chen Xiao, Liu Lei, Zhao Shaorong, Liu Jingjing, Ou Yang, Guo Min, Qi Chunchun, Li Zhaoxian, Shi Jie, Liu Yuxin, Shuai Qiuying, Zuo Siyu, Hu Huayu, Yu Tianwen, Wang Yanjing, Feng Mengdan, Lv Jianying, Wang Hang, Sun Peiqing, Zhang Jin, Wang Longlong, Shi Yi, Yang Shuang

机构信息

Tianjin Key Laboratory of Tumor Microenvironment and Neurovascular Regulation, School of Medicine, Nankai University, Tianjin, PR China.

Tianjin Medical University Cancer Institute & Hospital, Tianjin, PR China.

出版信息

Nat Commun. 2025 Jul 1;16(1):6011. doi: 10.1038/s41467-025-61088-3.

Abstract

Upon penetrating the basement membrane, breast cancer cells directly interact with their surrounding adipose tissue, which forms a unique tumor-associated adipose microenvironment (TAME). However, the underlying mechanism of lipid metabolic remodeling in the TAME remains elusive. Herein, we report a Zeb1-orchestrated bidirectional communication between breast cancer cells and their adjacent cancer-associated adipocytes (CAAs). At the molecular level, breast cancer cells, through the secretion of adrenomedullin (AM), induce downregulation of Zeb1 expression to activate the Atgl/Hsl/Scd-dependent lipolysis in CAAs, resulting in the release of palmitoleic acid (POA) into the TAME. In turn, the increased POA in breast cancer competes with arachidonic acid (ARA) for the phospholipid synthesis, leaving more ARA is utilized for PDG production to trigger the malignant progression of breast cancer and AM production. Importantly, disruption of Zeb1-dependent lipolytic activity and/or membrane phospholipid remodeling within the TAME dramatically diminishes the aggressiveness of breast cancer in vitro and in vivo.

摘要

穿透基底膜后,乳腺癌细胞直接与其周围的脂肪组织相互作用,形成独特的肿瘤相关脂肪微环境(TAME)。然而,TAME中脂质代谢重塑的潜在机制仍不清楚。在此,我们报道了一种由Zeb1精心策划的乳腺癌细胞与其相邻的癌症相关脂肪细胞(CAA)之间的双向通讯。在分子水平上,乳腺癌细胞通过分泌肾上腺髓质素(AM)诱导Zeb1表达下调,从而激活CAA中依赖于Atgl/Hsl/Scd的脂肪分解,导致棕榈油酸(POA)释放到TAME中。反过来,乳腺癌中增加的POA与花生四烯酸(ARA)竞争磷脂合成,使更多的ARA用于PDG生成,从而触发乳腺癌的恶性进展和AM生成。重要的是,破坏TAME中依赖于Zeb1的脂肪分解活性和/或膜磷脂重塑会显著降低乳腺癌在体外和体内的侵袭性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验