Medicine

How Exercise Proteins May Protect Against Cancer Development

How the science connects

BiomarkerExercise physiologyCancer epidemiology

AI Insight

This study investigated whether circulating proteins act as biological intermediaries between physical activity and cancer risk using data from approximately 100,000 UK Biobank participants. While higher physical activity was causally associated with reduced risk of breast, colorectal, and prostate cancers through Mendelian randomization analysis, the researchers found limited evidence that the 436 proteins associated with physical activity actually mediate these protective effects. The findings suggest these proteins function primarily as biomarkers of physical activity rather than causal mechanisms explaining how exercise reduces cancer risk.


Understanding the biological pathways through which physical activity prevents cancer could help identify new therapeutic targets and optimize exercise recommendations for cancer prevention. However, this study indicates the relationship may be more complex than previously thought, requiring further investigation into alternative mechanisms beyond circulating protein levels.


⚠️ Preprint – Noch nicht peer-reviewed

Dieser Artikel wurde noch nicht von unabhängigen Experten begutachtet. Die Ergebnisse sind vorläufig und sollten mit Vorsicht interpretiert werden.

Introduction Higher physical activity (PA) is associated with lower risk of several cancers, but the biological mechanisms underlying these associations remain unclear. We integrated observational and Mendelian randomization (MR) approaches to investigate circulating proteins as potential intermediates linking PA to cancer risk. Methods We analysed accelerometer-derived PA measures (~100,000 participants), circulating protein levels (~53,000 participants) derived using the Olink Explore 3072 panel and cancer incidence (breast, colorectal, endometrial, and prostate cancers) via linked registry data among UK Biobank (UKB) participants. Observational associations were assessed using regression models and Cox proportional hazard models adjusting for demographic, lifestyle, and clinical covariates, including body mass index (BMI). Proteins associated with both overall acceleration average and cancer incidence were taken forward in a two-sample and two-step MR analyses using genome-wide association data. Results Higher overall acceleration average was observationally associated with lower risk of breast, colorectal, and endometrial cancer, with attenuation after BMI adjustment for endometrial and colorectal cancer, and a positive association with prostate cancer. MR analyses supported a protective causal effect of higher overall PA on breast, colorectal, and prostate cancer risk, and suggested a much larger effect than observational analyses. Overall, PA was observationally associated with 436 circulating proteins of which 44 were also associated with incident cancer risk. MR analyses provided some support that TNFSRF13B was influenced by physical activity in the same direction as the observational analyses but found conflicting evidence for an effect of TNFSRF13B on breast cancer, although the MR analysis is consistent with a protective effect of physical activity on breast cancer risk. Conclusions While higher overall physical activity appears to causally reduce risk of several cancers, circulating proteins associated with PA largely do not show strong evidence of being intermediates of these effects, suggesting they may act primarily as biomarkers of physical activity rather than causal intermediates.

Source: Exploring proteins as intermediates between physical activity and cancer in UK biobank