首页> 美国卫生研究院文献>Cancers >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
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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

机译:脂肪细胞和肿瘤细胞之间的旁分泌相互作用招募和修改巨噬细胞对乳腺肿瘤微环境:肥胖和​​炎症在乳房脂肪组织中的作用。

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摘要

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.
机译:肥胖与乳腺癌(BC)之间的关系集中在血清因素上。然而,乳腺含有脂肪组织(AT),其可使脂肪细胞与肿瘤细胞之间的串扰促进肿瘤巨噬细胞的募集。我们假设肥胖女性的乳房AT(bAT)会发炎,并且在乳腺癌的发展中起主要作用。使用小鼠巨噬细胞,乳腺肿瘤细胞和脂肪细胞的共培养物,在体外检查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(单独或组合使用)。在细胞上清液中,Luminex鉴定了具有趋化性和其他促肿瘤功能的其他分子。专注于已证明在乳腺癌发病机制中起着重要作用的脂肪因子瘦素表明它可调节巨噬细胞表型和功能。体内实验表明,肥胖小鼠的乳腺肿瘤更大,并且来自肥胖肿瘤承担者的bAT所含的巨噬细胞/ CLS和肥大性脂肪细胞的数量要多于来自肥胖肿瘤承担者的bAT,从而证实它更易发炎。而且,与瘦小鼠相比,肥胖患者离肿瘤远处的bAT发炎程度更高。我们的结果表明,bAT在肥胖症的乳腺癌发展中起作用。

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