Hillers-Ziemer Lauren E, McMahon Rachel Q, Hietpas Margaret, Paderta Gretchen, LeBeau Jennelle, McCready Jessica, Arendt Lisa M
Program in Cellular and Molecular Biology, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA.
Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Drive, Madison, WI 53706, USA.
Cancers (Basel). 2020 Feb 21;12(2):502. doi: 10.3390/cancers12020502.
Obesity is correlated with worsened prognosis and treatment resistance in breast cancer. Macrophage-targeted therapies are currently in clinical trials, however, little is known about how obesity may impact treatment efficacy. Within breast adipose tissue, obesity leads to chronic, macrophage-driven inflammation, suggesting that obese breast cancer patients may benefit from these therapies. Using a high fat diet model of obesity, we orthotopically transplanted cancer cell lines into the mammary glands of obese and lean mice. We quantified changes in tumor invasiveness, angiogenesis and metastasis, and examined the efficacy of macrophage depletion to diminish tumor progression in obese and lean mice. Mammary tumors from obese mice grew significantly faster, were enriched for cancer stem-like cells (CSCs) and were more locally invasive and metastatic. Tumor cells isolated from obese mice demonstrated enhanced expression of stem cell-related pathways including and . Despite more rapid growth, mammary tumors from obese mice had reduced necrosis, higher blood vessel density, and greater macrophage recruitment. Depletion of macrophages in obese tumor-bearing mice resulted in increased tumor necrosis, reduced endothelial cells, and enhanced recruitment of CD8 T cells compared to IgG-treated controls. Macrophages may be an important clinical target to improve treatment options for obese breast cancer patients.
肥胖与乳腺癌预后恶化及治疗抵抗相关。针对巨噬细胞的疗法目前正处于临床试验阶段,然而,关于肥胖如何影响治疗效果却知之甚少。在乳腺脂肪组织中,肥胖会导致由巨噬细胞驱动的慢性炎症,这表明肥胖的乳腺癌患者可能会从这些疗法中获益。我们利用高脂肪饮食诱导的肥胖模型,将癌细胞系原位移植到肥胖和瘦小鼠的乳腺中。我们量化了肿瘤侵袭性、血管生成和转移的变化,并研究了巨噬细胞清除对肥胖和瘦小鼠肿瘤进展的抑制效果。肥胖小鼠的乳腺肿瘤生长明显更快,富含癌干细胞样细胞(CSC),且更具局部侵袭性和转移性。从肥胖小鼠分离出的肿瘤细胞显示出包括[此处原文缺失具体通路名称]和[此处原文缺失具体通路名称]在内的干细胞相关通路的表达增强。尽管生长更快,但肥胖小鼠的乳腺肿瘤坏死减少、血管密度更高且巨噬细胞募集更多。与IgG处理的对照组相比,肥胖荷瘤小鼠体内巨噬细胞的清除导致肿瘤坏死增加、内皮细胞减少以及CD8 T细胞募集增强。巨噬细胞可能是改善肥胖乳腺癌患者治疗选择的一个重要临床靶点。