Sex differences in colonic gene expression and fecal microbiota composition in a mouse model of obesity-associated colorectal cancer

被引:0
|
作者
Chang, Yoo-Mee [1 ]
Kang, Yoo-Ree [1 ]
Lee, Yu-Gyeong [1 ]
Sung, Mi-Kyung [1 ]
机构
[1] Sookmyung Womens Univ, Dept Food & Nutr, Coll Human Ecol, 100 Cheongpa Ro 47 Gil, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
ESTROGEN PLUS PROGESTIN; INFLAMMATION; CARCINOGENESIS; DIET; PATHWAY; TARGET;
D O I
10.1038/s41598-024-53861-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study investigated the sex-specific correlation between obesity and colorectal cancer emphasizing a more pronounced association in males. Estrogen, chromosomal genes, and gut bacteria were assessed in C57BL6/J male, female and ovariectomized (OVX) female mice, subjected to either a low-fat diet (LFD) or high-fat diet (HFD) for 14 weeks. Induction of colon tumor involved azoxymethane (10 mg/kg) administration, followed by three cycles of dextran sulfate sodium. Male mice on HFD exhibited higher final body weight and increased colon tumors compared to females. Colonic mucin 2 expression was significantly higher in females. HFD-modulated differentially expressed genes numbered 290 for males, 64 for females, and 137 for OVX females. Only one up-regulated gene (Gfra3) overlapped between females and OVX females, while two down-regulated genes (Thrsp and Gbp11) overlapped between males and OVX females. Genes up-regulated by HFD in males were linked to cytokine-cytokine interaction, HIF-1 signaling pathway, central carbon metabolism in cancer. Sex-specific changes in gut microbial composition in response to HFD were observed. These findings suggest a male-specific vulnerability to HFD-induced colon tumor formation, implicating key genes and colonic bacteria in colon tumorigenesis.
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页数:14
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