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

Author:

Bowers Laura W.1ORCID,Glenny Elaine M.2ORCID,Punjala Arunima3ORCID,Lanman Nadia A.45ORCID,Goldbaum Audrey6ORCID,Himbert Caroline7ORCID,Montgomery Stephanie A.8ORCID,Yang Peiying9ORCID,Roper Jatin10ORCID,Ulrich Cornelia M.7ORCID,Dannenberg Andrew J.11ORCID,Coleman Michael F.2ORCID,Hursting Stephen D.1212ORCID

Affiliation:

1. 1Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

2. 2Department of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

3. 3School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

4. 4Center for Cancer Research, Purdue University, West Lafayette, Indiana.

5. 5Department of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.

6. 6Department of Nutrition Science, Purdue University, West Lafayette, Indiana.

7. 7Department of Population Health Sciences, University of Utah, Salt Lake City, Utah.

8. 8Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

9. 9Department of Palliative, Rehabilitation, and Integrative Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas.

10. 10Department of Medicine, Duke University, Durham, North Carolina.

11. 11Department of Medicine (retired), Weill Cornell Medical College, New York, New York.

12. 12Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina.

Abstract

Abstract 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 obesity enhances murine colon carcinogenesis and expression of numerous tumoral procancer and immunosuppressive pathways. Moreover, we establish that weight loss via LFD and/or the NSAID sulindac mitigate procancer effects of obesity.

Funder

NIH

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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