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脂肪细胞与肿瘤细胞之间的旁分泌相互作用招募并改变巨噬细胞至乳腺肿瘤微环境:肥胖与炎症在乳腺脂肪组织中的作用

Paracrine Interactions between Adipocytes and Tumor Cells Recruit and Modify Macrophages to the Mammary Tumor Microenvironment: The Role of Obesity and Inflammation in Breast Adipose Tissue.

作者信息

Santander Ana M, Lopez-Ocejo Omar, Casas Olivia, Agostini Thais, Sanchez Lidia, Lamas-Basulto Eduardo, Carrio Roberto, Cleary Margot P, Gonzalez-Perez Ruben R, Torroella-Kouri Marta

机构信息

Department of Microbiology and Immunology, University of Miami Miller School of Medicine, 1600 NW 10th Ave, Miami, FL 33136, USA.

Hormel Institute, University of Minnesota, Austin, MN 55912, USA.

出版信息

Cancers (Basel). 2015 Jan 15;7(1):143-78. doi: 10.3390/cancers7010143.

Abstract

The relationship between obesity and breast cancer (BC) has focused on serum factors. However, the mammary gland contains adipose tissue (AT) which may enable the crosstalk between adipocytes and tumor cells contributing to tumor macrophage recruitment. We hypothesize that the breast AT (bAT) is inflamed in obese females and plays a major role in breast cancer development. The effects of this interplay on macrophage chemotaxis were examined in vitro, using co-cultures of mouse macrophages, mammary tumor cells and adipocytes. Macrophages were exposed to the adipocyte and tumor paracrine factors leptin, CCL2 and lauric acid (alone or in combinations). In cell supernatants Luminex identified additional molecules with chemotactic and other pro-tumor functions. Focus on the adipokine leptin, which has been shown to have a central role in breast cancer pathogenesis, indicated it modulates macrophage phenotypes and functions. In vivo experiments demonstrate that mammary tumors from obese mice are larger and that bAT from obese tumor-bearers contains higher numbers of macrophages/CLS and hypertrophic adipocytes than bAT from lean tumor-bearers, thus confirming it is more inflamed. Also, bAT distal from the tumor is more inflamed in obese than in lean mice. Our results reveal that bAT plays a role in breast cancer development in obesity.

摘要

肥胖与乳腺癌(BC)之间的关系一直聚焦于血清因子。然而,乳腺含有脂肪组织(AT),这可能使脂肪细胞与肿瘤细胞之间产生相互作用,进而促进肿瘤巨噬细胞的募集。我们推测,肥胖女性的乳腺脂肪组织(bAT)会发生炎症反应,并在乳腺癌发展中起主要作用。利用小鼠巨噬细胞、乳腺肿瘤细胞和脂肪细胞的共培养体系,在体外研究了这种相互作用对巨噬细胞趋化性的影响。巨噬细胞暴露于脂肪细胞和肿瘤旁分泌因子瘦素、CCL2和月桂酸(单独或组合)中。在细胞上清液中,Luminex技术鉴定出了其他具有趋化和其他促肿瘤功能的分子。聚焦于脂肪因子瘦素,它已被证明在乳腺癌发病机制中起核心作用,研究表明它可调节巨噬细胞的表型和功能。体内实验表明,肥胖小鼠的乳腺肿瘤更大,且肥胖荷瘤小鼠的bAT中巨噬细胞/CLS和肥大脂肪细胞的数量高于瘦荷瘤小鼠的bAT,从而证实其炎症反应更严重。此外,与瘦小鼠相比,肥胖小鼠肿瘤远端的bAT炎症反应更明显。我们的研究结果表明,bAT在肥胖相关的乳腺癌发展中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4e8/4381255/fd66c21a649b/cancers-07-00143-g001.jpg

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