Potential anti-cancer drugs commonly used for other indications
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
25544649
DOI
10.2174/1568009615666141229152812
PII: CCDT-EPUB-64230
Knihovny.cz E-resources
- MeSH
- Anthelmintics therapeutic use MeSH
- Antihypertensive Agents therapeutic use MeSH
- Cytostatic Agents therapeutic use MeSH
- Hypoglycemic Agents therapeutic use MeSH
- Humans MeSH
- Neoplasms drug therapy MeSH
- Drug Repositioning * MeSH
- Antineoplastic Agents therapeutic use MeSH
- Psychotropic Drugs therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Anthelmintics MeSH
- Antihypertensive Agents MeSH
- Cytostatic Agents MeSH
- Hypoglycemic Agents MeSH
- Antineoplastic Agents MeSH
- Psychotropic Drugs MeSH
An increasing resistance of mammalian tumor cells to chemotherapy along with the severe side effects of commonly used cytostatics has raised the urgency in the search for new anti-cancer agents. Several drugs originally approved for indications other than cancer treatment have recently been found to have a cytostatic effect on cancer cells. These drugs could be expediently repurposed as anti-cancer agents, since they have already been tested for toxicity in humans and animals. The groups of newly recognized potential cytostatics discussed in this review include benzimidazole anthelmintics (albendazole, mebendazole, flubendazole), anti-hypertensive drugs (doxazosin, propranolol), psychopharmaceuticals (chlorpromazine, clomipramine) and antidiabetic drugs (metformin, pioglitazone). All these drugs have a definite potential to be used especially in combinations with other cytostatics; the chemotherapy targeting of multiple sites now represents a promising approach in cancer treatment. The present review summarizes recent information about the anti-cancer effects of selected drugs commonly used for other medical indications. Our aim is not to collect all the reported results, but to present an overview of various possibilities. Advantages, disadvantages and further perspectives regarding individual drugs are discussed and evaluated.
References provided by Crossref.org
Flubendazole exhibits anti-glioblastoma effect by inhibiting STAT3 and promoting cell cycle arrest
Benzimidazoles Downregulate Mdm2 and MdmX and Activate p53 in MdmX Overexpressing Tumor Cells