Weight Loss and/or Sulindac Mitigate Obesity-associated Transcriptome, Microbiome, and Protumor Effects in a Murine Model of Colon Cancer

被引:4
作者
Bowers, Laura W. [1 ]
Glenny, Elaine M. [2 ]
Punjala, Arunima [3 ]
Lanman, Nadia A. [4 ,5 ]
Goldbaum, Audrey [6 ]
Himbert, Caroline [7 ]
Montgomery, Stephanie A. [8 ]
Yang, Peiying [9 ]
Roper, Jatin [10 ]
Ulrich, Cornelia M. [7 ]
Dannenberg, Andrew J. [11 ]
Coleman, Michael F. [2 ]
Hursting, Stephen D. [1 ,2 ,12 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Nutr, 135 Dauer Dr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Chapel Hill, NC 27599 USA
[4] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47907 USA
[5] Purdue Univ, Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[6] Purdue Univ, Dept Nutr Sci, W Lafayette, IN 47907 USA
[7] Univ Utah, Dept Populat Hlth Sci, Salt Lake City, UT USA
[8] Univ N Carolina, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[9] Univ Texas MD Anderson Canc Ctr, Dept Palliat Rehabil & Integrat Med, Houston, TX 77030 USA
[10] Duke Univ, Dept Med, Durham, NC USA
[11] Weill Cornell Med Coll, Dept Med, New York, NY USA
[12] Univ North Carolina Chapel Hill, Nutr Res Inst, Kannapolis, NC USA
关键词
RECEPTOR-TYPE-II; COLORECTAL-CANCER; RISK; GROWTH; CARCINOGENESIS; CHEMOPREVENTION; INDEX; TUMORIGENESIS; INACTIVATION; METAANALYSIS;
D O I
10.1158/1940-6207.CAPR-21-0531
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
? Obesity is associated with an increased risk of colon cancer. Our current study examines whether weight loss and/or treatment with the NSAID sulindac suppresses the protumor effects of obesity in a mouse model of colon cancer. Azoxymethane-treated male FVB/N mice were fed a low-fat diet (LFD) or high-fat diet (HFD) for 15 weeks, then HFD mice were randomized to remain on HFD (obese) or switch to LFD [formerly obese (FOb-LFD)]. Within the control (LFD), obese, and FOb-LFD groups, half the mice started sulindac treatment (140 ppm in the diet). All mice were euthanized 7 weeks later. FOb-LFD mice had intermediate body weight levels, lower than obese but higher than control (P < 0.05). Sulindac did not affect body weight. Obese mice had greater tumor multiplicity and burden than all other groups (P < 0.05). Transcriptomic profiling indicated that weight loss and sulindac each modulate the expression of tumor genes related to invasion and may promote a more antitumor immune landscape. Furthermore, the fecal microbes Coprobacillus, Prevotella, and Akkermansia muciniphila were positively correlated with tumor multiplicity and reduced by sulindac in obese mice. Coprobacillus abundance was also decreased in FOb-LFD mice. In sum, weight loss and sulindac treatment, alone and in combination, reversed the effects of chronic obesity on colon tumor multiplicity and burden. Our findings suggest that an investigation regarding the effects of NSAID treatment on colon cancer risk and/or progression in obese individuals is warranted, particularly for those unable to achieve moderate weight loss. Prevention Relevance: Obesity is a colon cancer risk and/or progression factor, but the underlying mechanisms are incompletely understood. Herein we demonstrate that obe-sity enhances murine colon carcinogenesis and expression of numerous tumoral procancer and immunosuppressive path-ways. Moreover, we establish that weight loss via LFD and/or the NSAID sulindac mitigate procancer effects of obesity.
引用
收藏
页码:481 / 495
页数:15
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