摘要:脂肪来源的单核细胞趋化蛋白-1在肥胖增强的男性乳腺癌模型中的致瘤性和代谢组学影响

Lin Yan, Sneha Sundaram, Bret M. Rust, M. Picklo, M. Bukowski
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引用次数: 0

摘要

乳腺癌是一种罕见但侵袭性的男性疾病。大约90%的男性乳腺癌为浸润性癌,其中25%在临床表现时有远处转移。肥胖是患乳腺癌的一个危险因素。单核细胞趋化蛋白-1 (MCP-1)是一种脂肪来源的细胞因子,其浓度因肥胖而升高。这项研究验证了脂肪来源的MCP-1与男性乳腺癌有关的假设。在2x2设计中,有或没有脂肪特异性Mcp-1基因敲低的雄性MMTV-PyMT小鼠[被称为Mcp-1-/-或野生型(WT)]被喂食标准AIN93G饮食或致肥性高脂肪饮食(HFD) 25周。AIN93G日粮和HFD分别含有16%和45%的大豆油能量。Mcp-1-/-小鼠脂肪Mcp-1表达低于WT小鼠。脂肪Mcp-1缺乏降低了喂食HFD的小鼠血浆Mcp-1浓度。无论基因型如何,喂食HFD的小鼠肿瘤进展率高于喂食AIN93G的小鼠(4679% vs 2430%)。与WT小鼠相比,Mcp-1-/-小鼠具有更长的肿瘤潜伏期(25.2周对18.0周),更低的肿瘤发病率(19%对56%),肿瘤进展率(2317%对472%)和肿瘤重量(0.23 g对0.64 g)。血浆代谢组学分析鉴定出87种代谢物,其中56种代谢物在四组中不同,其中24种在饮食中不同,22种在基因型中不同。稀疏偏最小二乘判别分析确定了四组中变化最大的10个主要代谢物。这些包括氨基酸(丙氨酸、异亮氨酸、亮氨酸、苯丙氨酸、苏氨酸和缬氨酸)和碳水化合物代谢物(富马酸、葡萄糖醛酸、己糖醛酸和苹果酸)。对鉴定的87种代谢物的综合通路分析表明,蛋白质生物合成和碳水化合物代谢途径在MMTV-PyMT小鼠中受到的干扰最大。总之,脂肪来源的MCP-1有助于乳腺肿瘤的发生,并改变雄性MMTV-PyMT小鼠的代谢。引文格式:林岩,Sneha Sundaram, Bret M. Rust, Matthew J. Picklo, Michael R. Bukowski。脂肪来源的单核细胞趋化蛋白-1在肥胖增强的男性乳腺癌模型中的致瘤性和代谢组学影响[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):2561。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 2561: Tumorigenic and metabolomic impacts of adipose-derived monocyte chemotactic protein-1 in a model of obesity-enhanced, male breast cancer
Breast cancer is a rare but aggressive disease in men. Approximately, 90% of all breast cancer in men are invasive carcinomas, 25% of which have distant metastasis at the time of clinical presentation. Obesity is a risk factor for breast cancer. Monocyte chemotactic protein-1 (MCP-1) is an adipose-derived cytokine whose concentrations are elevated by obesity. This study tested the hypothesis that adipose-derived MCP-1 contributes to male breast cancer. In a 2x2 design, male MMTV-PyMT mice with or without adipose specific Mcp-1 knockdown [designated as Mcp-1-/- or wild-type (WT)] were fed the standard AIN93G diet or an obesogenic, high-fat diet (HFD) for 25 weeks. The AIN93G diet and HFD contained 16% and 45% of energy from soybean oil, respectively. Mcp-1-/- mice had lower adipose Mcp-1 expression than WT mice. Adipose Mcp-1 deficiency reduced plasma concentrations of MCP-1 in mice fed the HFD. Mice fed the HFD had a greater tumor progression rate than mice fed the AIN93G diet (4679% vs 2430%), regardless of genotype. Mcp-1-/- mice, compared to WT mice, had a longer tumor latency (25.2 weeks vs 18.0 weeks) and lower tumor incidence (19% vs 56%), tumor progression rate (2317% vs 4792%), and tumor weights (0.23 g vs 0.64 g). Metabolomic analysis of plasma identified 87 metabolites, 56 of which differed among the four groups, including 24 that differed between the diets and 22 that differed between the genotypes. Sparse partial least squares-discriminant analysis identified 10 major metabolites that were altered the most among the four groups. These included amino acids (alanine, isoleucine, leucine, phenylalanine, threonine, and valine) and carbohydrate metabolites (fumaric acid, glucuronic acid, hexuronic acid, and malic acid). The integrated pathway analysis of the 87 identified metabolites showed that protein biosynthesis and carbohydrate metabolism pathways are the most disturbed in MMTV-PyMT mice. In conclusion, adipose-derived MCP-1 contributes to mammary tumorigenesis and alters metabolism in male MMTV-PyMT mice. Citation Format: Lin Yan, Sneha Sundaram, Bret M. Rust, Matthew J. Picklo, Michael R. Bukowski. Tumorigenic and metabolomic impacts of adipose-derived monocyte chemotactic protein-1 in a model of obesity-enhanced, male breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2561.
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