Body Weight Correlates with Molecular Variances in Patients with Cancer

Author:

Huang Fengyuan12ORCID,Xu Peng12ORCID,Yue Zongliang12ORCID,Song Yuwei12ORCID,Hu Kaili12ORCID,Zhao Xinyang3ORCID,Gao Min14ORCID,Chong Zechen125ORCID

Affiliation:

1. 1Informatics Institute, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.

2. 2Department of Genetics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.

3. 3Department of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, Kansas.

4. 4Department of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.

5. 5HudsonAlpha Institute for Biotechnology, Huntsville, Alabama.

Abstract

Abstract Overweight and obesity are identified by a high body mass index (BMI) and carry significant health risks due to associated comorbidities. Although epidemiologic data connect overweight/obesity with 13 cancer types, a better understanding of the molecular mechanisms underlying this correlation is needed to improve prevention and treatment strategies. In this study, we conducted a comprehensive analysis of molecular differences between overweight or obese patients and normal weight patients across 14 different cancer types from The Cancer Genome Atlas. Using the propensity score weighting algorithm to control for confounding factors, obesity-specific mutational features were identified, such as higher mutation burden in rectal cancer and biased mutational signatures in other cancers. Differentially expressed genes (DEG) in tumors from patients with overweight/obesity were predominantly upregulated and enriched in inflammatory and hormone-related pathways. These DEGs were significantly associated with survival rates in various cancer types, highlighting the impact of elevated body fat on gene expression profiles and clinical outcomes in patients with cancer. Interestingly, while high BMI seemed to have a negative impact on most cancer types, the normal weight–biased mutational and gene expression patterns indicated overweight/obesity may be beneficial in endometrial cancer, suggesting the presence of an “obesity paradox” in this context. Body fat also significantly impacted the tumor microenvironment by modulating immune cell infiltration, underscoring the importance of understanding the interplay between weight and immune response in cancer progression. Together, this study systematically elucidates the molecular differences corresponding to body weight in multiple cancer types, offering potentially critical insights for developing precision therapy for patients with cancer. Significance: Elucidation of the complex interplay between body weight and the molecular landscape of cancer could potentially guide tailored therapies and improve patient management amid the global obesity crisis.

Funder

National Institute of General Medical Sciences

National Institute on Minority Health and Health Disparities

National Heart, Lung, and Blood Institute

Publisher

American Association for Cancer Research (AACR)

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