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The Gut-Adipose-Tumor Axis in Obesity-Related Cancer
Juan Feng1, Yiyang Huang1, Sien Lai1
1Guangdong Provincial Engineering and Technology Research Center for Gene Editing, School of Medicine, Foshan University, Foshan 528000, China.
Obesity drives cancer through the gut-adipose-tumor axis, a complex interaction between the gut microbiome, fat tissue, and tumors. Understanding this axis offers new avenues for obesity-related cancer prevention and treatment.
Area of Science:
- Oncology
- Microbiome Research
- Metabolic Syndrome
Background:
- The global obesity epidemic is a significant risk factor for cancer incidence and mortality.
- The gut-adipose-tumor axis is increasingly recognized as a key mediator in obesity-related carcinogenesis.
- This axis involves intricate crosstalk between the gut microbiome, adipose tissue, and the tumor microenvironment.
Purpose of the Study:
- To review the current understanding of the gut-adipose-tumor axis.
- To explore its epidemiological, pathophysiological, and therapeutic implications.
- To identify future research directions for obesity-related cancers.
Main Methods:
- Literature review synthesizing current evidence on the gut-adipose-tumor axis.
- Analysis of the mechanisms linking obesity, gut dysbiosis, adipose tissue dysfunction, and cancer progression.
- Examination of therapeutic strategies targeting this axis.
Main Results:
- Obesity-induced gut dysbiosis promotes systemic inflammation and alters metabolite profiles.
- Dysfunctional adipose tissue, influenced by gut signals, exacerbates chronic inflammation and secretes cancer-promoting mediators.
- The combined effects create a pro-carcinogenic environment that impacts the tumor microenvironment.
Conclusions:
- The gut-adipose-tumor axis is a critical integrated system in obesity-related carcinogenesis.
- Targeting this axis presents novel opportunities for cancer prevention and treatment strategies.
- Further research is crucial for elucidating mechanisms and developing effective therapies for obesity-related cancers.
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