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Low Doses Naltrexone: The Potential Benefit Effects for its Use in Patients with Cancer
Ricardo David Couto1, Bruno Jose Dumêt Fernandes2
1Clinical Biochemistry Laboratory, Department of Clinical and Toxicological Analysis, Faculty of Pharmacy, Federal University of Bahia/UFBA, Salvador, Bahia, Brazil.
Abstract:
Naltrexone (NTX) is an opioid antagonist that inhibits cell proliferation in vivo when administered in low doses. Naltrexone in low doses can reduce tumor growth by interfering with cell signalling as well as by modifying the immune system. It acts as an Opioid Growth Factor receptor (OGFr) antagonist and the OGF-OGFr axis is an inhibitory biological pathway present in human cancer cells and tissues, being a target for the treatment with naltrexone low-dose (LDN). Clinical trials have proposed a unique mechanism(s) allowing LDN to affect tumors. LDN shows promising results for people with primary cancer of the bladder, breast, liver, lung, lymph nodes, colon and rectum. This short review provides further evidence to support the role of LDN as an anticancer agent.
Insights
Low-dose naltrexone (LDN) is an opioid antagonist that inhibits cancer cell proliferation and tumor growth. This review supports LDN as a promising anticancer agent targeting the OGF-OGFr pathway in various cancers.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Naltrexone (NTX), an opioid antagonist, inhibits cell proliferation in vivo at low doses.
- The OGF-OGFr axis is an inhibitory pathway in human cancers, targeted by low-dose naltrexone (LDN).
Purpose of the Study:
- To provide evidence supporting the role of LDN as an anticancer agent.
- To highlight LDN's potential in treating various primary cancers.
Main Methods:
- Review of clinical trials and existing evidence on LDN's anticancer mechanisms.
- Analysis of LDN's effects on cell signaling and immune modulation.
Main Results:
- LDN reduces tumor growth by interfering with cell signaling and modifying the immune system.
- LDN acts as an Opioid Growth Factor receptor (OGFr) antagonist.
- Promising results observed in clinical trials for bladder, breast, liver, lung, lymph node, and colorectal cancers.
Conclusions:
- LDN demonstrates significant potential as an anticancer agent.
- The OGF-OGFr pathway is a viable target for LDN therapy in oncology.
- Further research and clinical application of LDN for cancer treatment are warranted.
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