Literature DB >> 31054863

Doxycycline, salinomycin, monensin and ivermectin repositioned as cancer drugs.

Anna Markowska1, Joanna Kaysiewicz2, Janina Markowska3, Adam Huczyński4.   

Abstract

Chemotherapy is one of the standard methods for the treatment of malignant tumors. It aims to cause lethal damage to cellular structures, mainly DNA. Noteworthy, in recent years discoveries of novel anticancer agents from well-known antibiotics have opened up new treatment pathways for several cancer diseases. The aim of this review article is to describe new applications for the following antibiotics: doxycycline (DOX), salinomycin (SAL), monensin (MON) and ivermectin (IVR) as they are known to show anti-tumor activity, but have not yet been introduced into standard oncological therapy. To date, these agents have been used for the treatment of a broad-spectrum of bacterial and parasitic infectious diseases and are widely available, which is why they were selected. The data presented here clearly show that the antibiotics mentioned above should be recognised in the near future as novel agents able to eradicate cancer cells and cancer stem cells (CSCs) across several cancer types.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anticancer antibiotic; Cancer stem cells; New anticancer agent; Off-target effect

Mesh:

Substances:

Year:  2019        PMID: 31054863     DOI: 10.1016/j.bmcl.2019.04.045

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  17 in total

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4.  The Battle against COVID 19 Pandemic: What we Need to Know Before we "Test Fire" Ivermectin.

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Review 6.  Targeting Reactive Oxygen Species Capacity of Tumor Cells with Repurposed Drug as an Anticancer Therapy.

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7.  Safety of inhaled ivermectin as a repurposed direct drug for treatment of COVID-19: A preclinical tolerance study.

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Review 9.  Recycling the Purpose of Old Drugs to Treat Ovarian Cancer.

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10.  Narasin inhibits tumor metastasis and growth of ERα‑positive breast cancer cells by inactivation of the TGF‑β/SMAD3 and IL‑6/STAT3 signaling pathways.

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