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从前肥胖小鼠的乳腺和肿瘤微环境的改变。

Alterations in the mammary gland and tumor microenvironment of formerly obese mice.

机构信息

Cancer Biology Program, University of Wisconsin-Madison, Madison, WI, 53705, USA.

Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, 53706, USA.

出版信息

BMC Cancer. 2023 Dec 1;23(1):1183. doi: 10.1186/s12885-023-11688-3.

Abstract

BACKGROUND

Obesity is a risk factor for breast cancer, and women with obesity that develop breast cancer have a worsened prognosis. Within the mammary gland, obesity causes chronic, macrophage-driven inflammation and adipose tissue fibrosis. Weight loss is a recommended intervention to resolve obesity, but the impact of weight loss on the mammary gland microenvironment and in tumors has not been well identified.

METHODS

To examine the effects of weight loss following obesity, mice were fed a high-fat diet for 16 weeks to induce obesity, then switched to a low-fat diet for 6 weeks. We examined changes in immune cells, including fibrocytes, which are myeloid lineage cells that have attributes of both macrophages and myofibroblasts, and collagen deposition within the mammary glands of non-tumor-bearing mice and within the tumors of mice that were transplanted with estrogen receptor alpha positive TC2 tumor cells.

RESULTS

In formerly obese mice, we observed reduced numbers of crown-like structures and fibrocytes in mammary glands, while collagen deposition was not resolved with weight loss. Following transplant of TC2 tumor cells into the mammary glands of lean, obese, and formerly obese mice, diminished collagen deposition and cancer-associated fibroblasts were observed in tumors from formerly obese mice compared to obese mice. Within tumors of obese mice, increased myeloid-derived suppressor cells and diminished CD8 T cells were identified, while the microenvironment of tumors of formerly obese mice were more similar to tumors from lean mice. When TC2 tumor cells were mixed with CD11bCD34 myeloid progenitor cells, which are the cells of origin for fibrocytes, and transplanted into mammary glands of lean and obese mice, collagen deposition within the tumors of both lean and obese was significantly greater than when tumor cells were mixed with CD11bCD34 monocytes or total CD45 immune cells.

CONCLUSIONS

Overall, these studies demonstrate that weight loss resolved some of the microenvironmental conditions within the mammary gland that may contribute to tumor progression. Additionally, fibrocytes may contribute to early collagen deposition in mammary tumors of obese mice leading to the growth of desmoplastic tumors.

摘要

背景

肥胖是乳腺癌的一个风险因素,而肥胖的乳腺癌患者预后更差。在乳腺中,肥胖会导致慢性、巨噬细胞驱动的炎症和脂肪组织纤维化。减肥是一种推荐的干预措施,可以解决肥胖问题,但减肥对乳腺微环境和肿瘤的影响尚未得到很好的确定。

方法

为了研究肥胖后减肥的效果,我们让小鼠喂食高脂肪饮食 16 周以诱导肥胖,然后切换到低脂肪饮食 6 周。我们检查了免疫细胞的变化,包括纤维母细胞,纤维母细胞是具有巨噬细胞和肌成纤维细胞特征的骨髓谱系细胞,以及非肿瘤负荷小鼠乳腺内和雌激素受体α阳性 TC2 肿瘤细胞移植小鼠肿瘤内的胶原沉积的变化。

结果

在以前肥胖的小鼠中,我们观察到乳腺中冠层样结构和纤维母细胞数量减少,而胶原沉积并未随体重减轻而消除。将 TC2 肿瘤细胞移植到瘦鼠、肥胖鼠和以前肥胖鼠的乳腺中后,与肥胖鼠相比,以前肥胖鼠的肿瘤中胶原沉积和癌相关成纤维细胞减少。在肥胖鼠的肿瘤中,发现髓源性抑制细胞增加,CD8 T 细胞减少,而以前肥胖鼠肿瘤的微环境更类似于瘦鼠的肿瘤。当 TC2 肿瘤细胞与 CD11bCD34 髓系祖细胞(纤维母细胞的起源细胞)混合并移植到瘦鼠和肥胖鼠的乳腺中时,与肿瘤细胞与 CD11bCD34 单核细胞或总 CD45 免疫细胞混合相比,肿瘤内的胶原沉积在瘦鼠和肥胖鼠中均显著增加。

结论

总的来说,这些研究表明,减肥解决了乳腺中一些可能促进肿瘤进展的微环境条件。此外,纤维母细胞可能导致肥胖小鼠乳腺肿瘤中早期胶原沉积,导致促结缔组织增生性肿瘤的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82af/10693119/fa5fd5322bf4/12885_2023_11688_Fig1_HTML.jpg

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