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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2024 pubmed 7 citations

Role of innate host defense proteins in oral cancerogenesis.

Winter. Jochen J; Jepsen. Søren S

Key Findings

  • Chronic inflammation, such as periodontitis, is a major driver of oral squamous cell carcinoma.
  • LL‑37 and other innate defense peptides can directly stimulate tumor growth by binding to growth‑promoting receptors and activating cancer‑related genes.
  • Bacterial challenges in the oral cavity can further amplify the tumor‑promoting effects of these peptides.

Practical Outcomes

  • If you’re using LL‑37 or similar peptides for antimicrobial or anti‑inflammatory purposes, be aware of a potential link to oral cancer, especially if you have chronic gum disease. Prioritize good oral hygiene and monitor any oral lesions. Consider limiting long‑term, high‑dose LL‑37 exposure until more safety data are available.

Summary

The review says that a natural antimicrobial peptide called LL‑37, which is part of our innate immune system, can sometimes act like a double‑edged sword in the mouth. While it helps fight infections, it may also bind to cell receptors and turn on genes that encourage oral cancer, especially when chronic gum disease or bacterial infections are present.

Abstract

It is nowadays well accepted that chronic inflammation plays a pivotal role in tumor initiation and progression. Under this aspect, the oral cavity is predestined to examine this connection because periodontitis is a highly prevalent chronic inflammatory disease and oral squamous cell carcinomas are the most common oral malignant lesions. In this review, we describe how particular molecules of the human innate host defense system may participate as molecular links between these two important chronic noncommunicable diseases (NCDs). Specific focus is directed toward antimicrobial polypeptides, such as the cathelicidin LL-37 and human defensins, as well as S100 proteins and alarmins. We report in which way these peptides and proteins are able to initiate and support oral tumorigenesis, showing direct mechanisms by binding to growth-stimulating cell surface receptors and/or indirect effects, for example, inducing tumor-promoting genes. Finally, bacterial challenges with impact on oral cancerogenesis are briefly addressed.

Study Information

Provider

pubmed

Year

2024

Date

2024-01-24T00:00:00.000Z

DOI

10.1111/prd.12552

Citations

7

References

236