Effect of genistein supplementation on microenvironment regulation of breast tumors in obese mice.

IF 7.4 1区 医学 Q1 Medicine
Shengzi Jin, Yingce Zheng, Ding Li, Xingyao Liu, Tingting Zhu, Shuang Wang, Zhonghua Liu, Yun Liu
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引用次数: 0

Abstract

Obesity is an important risk factor for breast cancer in women before and after menopause. Adipocytes, key mediators in the tumor microenvironment, play a pivotal role in the relationship between obesity with cancer. However, the potential of dietary components in modulating this relationship remains underexplored. Genistein, a soy-derived isoflavone, has shown promise in reducing breast cancer risk, attenuating obesity-associated inflammation, and improving insulin resistance. However, there are no reports examining whether genistein has the ability to reduce the effects of obesity on breast tumor development. In this study, we constructed a mammary tumor model in ovariectomized obese mice and examined the effects of genistein on body condition and tumor growth. Moreover, the effects of genistein on the tumor microenvironment were examined via experimental observation of peritumoral adipocytes and macrophages. In addition, we further investigated the effect of genistein on adipocyte and breast cancer cell crosstalk via coculture experiments. Our findings indicate that dietary genistein significantly alleviates obesity, systemic inflammation, and metabolic disorders induced by a high-fat diet in ovariectomized mice. Notably, it also inhibits tumor growth in vivo. The impact of genistein extends to the tumor microenvironment, where it reduces the production of cancer-associated adipocytes (CAAs) and the recruitment of M2d-subtype macrophages. In vitro, genistein mitigates the transition of adipocytes into CAAs and inhibits the expression of inflammatory factors by activating PPAR-γ pathway and degrading nuclear NF-κB. Furthermore, it impedes the acquisition of invasive properties and epithelial‒mesenchymal transition in breast cancer cells under CAA-induced inflammation, disrupting the Wnt3a/β-catenin pathway. Intriguingly, the PPAR-γ inhibitor T0070907 counteracted the effects of genistein in the coculture system, underscoring the specificity of its action. Our study revealed that genistein can mitigate the adverse effects of obesity on breast cancer by modulating the tumor microenvironment. These findings provide new insights into how genistein intake and a soy-based diet can reduce breast cancer risk.

补充染料木素对肥胖小鼠乳腺肿瘤微环境调控的影响
肥胖是绝经前后妇女罹患乳腺癌的一个重要风险因素。脂肪细胞是肿瘤微环境的关键介质,在肥胖与癌症的关系中起着关键作用。然而,膳食成分在调节这种关系方面的潜力仍未得到充分探索。大豆中提取的异黄酮--染料木素在降低乳腺癌风险、减轻肥胖相关炎症反应和改善胰岛素抵抗方面表现出良好的前景。然而,目前还没有报告显示染料木素是否能够减少肥胖对乳腺肿瘤发生的影响。在这项研究中,我们用卵巢切除的肥胖小鼠构建了乳腺肿瘤模型,并考察了染料木素对身体状况和肿瘤生长的影响。此外,我们还通过实验观察瘤周脂肪细胞和巨噬细胞,研究了染料木素对肿瘤微环境的影响。此外,我们还通过共培养实验进一步研究了染料木素对脂肪细胞和乳腺癌细胞串联的影响。我们的研究结果表明,膳食中的染料木素能明显减轻卵巢切除小鼠因高脂肪饮食引起的肥胖、全身炎症和代谢紊乱。值得注意的是,它还能抑制体内肿瘤的生长。染料木素的影响延伸到肿瘤微环境,它能减少癌症相关脂肪细胞(CAA)的生成和 M2d 亚型巨噬细胞的招募。在体外,染料木素通过激活 PPAR-γ 通路和降解核 NF-κB 来缓解脂肪细胞向 CAA 的转化,并抑制炎症因子的表达。此外,在 CAA 诱导的炎症作用下,它还能破坏 Wnt3a/β-catenin 通路,从而阻碍乳腺癌细胞获得侵袭性和上皮-间质转化。耐人寻味的是,PPAR-γ抑制剂T0070907在共培养系统中抵消了染料木素的作用,强调了染料木素作用的特异性。我们的研究发现,染料木素可以通过调节肿瘤微环境来减轻肥胖对乳腺癌的不利影响。这些发现为人们提供了新的视角,让人们了解摄入染料木素和以大豆为基础的饮食是如何降低乳腺癌风险的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
12.00
自引率
0.00%
发文量
76
审稿时长
12 weeks
期刊介绍: Breast Cancer Research, an international, peer-reviewed online journal, publishes original research, reviews, editorials, and reports. It features open-access research articles of exceptional interest across all areas of biology and medicine relevant to breast cancer. This includes normal mammary gland biology, with a special emphasis on the genetic, biochemical, and cellular basis of breast cancer. In addition to basic research, the journal covers preclinical, translational, and clinical studies with a biological basis, including Phase I and Phase II trials.
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