# Parasitic Infections and Carcinogenesis: Molecular Mechanisms, Immune Modulation, and Emerging Therapeutic Strategies

**Authors:** Marta Pawłowska, Dorian Jarek, Jan Milanowski, Karolina Szewczyk-Golec

PMC · DOI: 10.32604/or.2025.071891 · Oncology Research · 2026-01-19

## TL;DR

This review explores how parasitic infections contribute to cancer by causing inflammation and immune changes, and highlights new treatment strategies.

## Contribution

The paper integrates parasitology and oncology to reveal novel mechanisms and therapeutic approaches for infection-induced cancers.

## Key findings

- Chronic parasitic infections drive tumorigenesis through inflammation and genomic instability.
- Parasite-derived exosomes reshape the tumor microenvironment.
- Emerging therapies include pathway inhibitors and parasite-based immunotherapies.

## Abstract

Parasitic infections are increasingly recognized as contributors to cancer development, yet the underlying oncogenic mechanisms remain insufficiently understood. Growing evidence from molecular oncology, immunology, and microbiome research suggests that chronic parasitic infections may drive tumorigenesis through sustained inflammation, deregulated signaling pathways, genomic instability, and the release of parasite-derived exosomes that reshape the tumor microenvironment. These insights underscore the need to integrate parasitology with cancer biology to understand infection-associated malignancies better. The aim of this narrative review is to synthesize current knowledge on how selected parasites contribute to cancer development and to highlight emerging therapeutic and diagnostic opportunities. We examine pathogens such as Schistosoma haematobium, Opisthorchis viverrini, Toxoplasma gondii, Plasmodium falciparum, and Leishmania spp., detailing their roles in chronic inflammation, immune modulation, and interactions with tumor-associated immune cells. The review further discusses parasite-induced immunosuppression, coinfections, and their cumulative impact on cancer risk. Additionally, we explore novel therapeutic approaches, including pathway inhibitors, epigenetic drugs, microbiome modulation, and engineered parasites. Future perspectives emphasize parasite-based immunotherapies, long-term epigenetic consequences of infection, and AI-driven multi-omics strategies for identifying oncogenic signatures. This review integrates advances from parasitology and oncology to provide new insights into biomarkers, targeted therapies, and mechanisms of infection-induced tumorigenesis. The literature search covered studies indexed in PubMed, Scopus, and Web of Science up to July 2025.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)
- **Species:** Schistosoma haematobium (taxon 6185), Opisthorchis viverrini (taxon 6198), Toxoplasma gondii (taxon 5811), Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Diseases:** Parasitic Infections (MESH:D010272), chronic inflammation (MESH:D007249), Carcinogenesis (MESH:D063646), infection (MESH:D007239), cancer (MESH:D009369)
- **Species:** Opisthorchis viverrini (Southeast Asian liver fluke, species) [taxon 6198], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Toxoplasma gondii (species) [taxon 5811], Schistosoma haematobium (species) [taxon 6185]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12848758/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12848758/full.md

## References

189 references — full list in the complete paper: https://tomesphere.com/paper/PMC12848758/full.md

---
Source: https://tomesphere.com/paper/PMC12848758