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The Inflammation-Mediated Bidirectional Relationship Between Cardiovascular Disease and Cancer
Shahzaib Chughtai1, Shofikur Shuhag2, Daksh Saksena3
1College of Medicine, Central Michigan University, 1632 Stone St, Saginaw, MI 48602, USA.
Diseases (Basel, Switzerland)
|July 27, 2026
Summary
Cancer and atherosclerotic cardiovascular disease (ASCVD) share biological pathways, driven by chronic inflammation. Targeting these shared mechanisms may offer dual benefits for preventing and treating both conditions.
Area of Science:
- Oncology
- Cardiology
- Inflammation Biology
Background:
- Cancer and atherosclerotic cardiovascular disease (ASCVD) are leading global causes of death.
- These diseases are increasingly recognized as biologically interconnected, not separate entities.
- Chronic inflammation is a potential key link, influencing shared pathways like endothelial dysfunction, oxidative stress, and thrombosis.
Purpose of the Study:
- To review the bidirectional relationship between ASCVD and cancer.
- To explore how shared inflammatory pathways connect these diseases.
- To discuss potential therapeutic strategies targeting these common mechanisms.
Main Methods:
- Narrative review of existing epidemiologic and mechanistic data.
- Analysis of scientific literature on cancer-cardiovascular disease links.
- Identification of shared biological pathways and risk factors.
Main Results:
- Epidemiologic data show increased cancer incidence in ASCVD patients and accelerated vascular disease in cancer survivors.
- Shared inflammatory pathways, including endothelial dysfunction and thrombosis, contribute to both cancer progression and ASCVD.
- Emerging evidence suggests targeting shared pathways may offer dual benefits.
Conclusions:
- ASCVD and cancer share common biological underpinnings, particularly chronic inflammation.
- Therapeutic strategies targeting shared pathways (e.g., statins, IL-6 inhibition, lifestyle changes) hold promise for dual prevention and treatment.
- Further biomarker-guided trials with integrated cardiovascular and oncologic endpoints are necessary to confirm causality and optimize management.
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