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From veterinary antibiotic to cancer therapy: revisiting anticancer potential of Monensin
Ali Darabniya1,2, Sara Shahriari3, Reza Fazeli3
1Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran. a-darabniya@razi.tums.ac.ir.
Abstract:
Monensin, a polyether ionophore widely used in veterinary medicine, has recently emerged as a multimodal anticancer candidate. This review provides a comprehensive overview of preclinical studies showing that monensin exerts selective cytotoxic and anti-progression effects across a wide range of malignancies. Its activity spans breast cancer to leukemia, reflecting both versatility and significant therapeutic potential. In breast cancer, monensin reduces proliferation, induces apoptosis, and enhances chemosensitivity, suggesting a role in combination therapies. In prostate cancer, it disrupts androgen receptor signaling, induces oxidative stress, and triggers mitochondria-dependent apoptosis. In pancreatic cancer, it suppresses EGFR signaling and promotes programmed cell death, while in ovarian and cervical cancers, it inhibits proliferation, migration, and invasion by modulating EGFR and MEK/ERK pathways and enhancing SUMOylation. In renal carcinoma, monensin induces cell-cycle arrest, autophagy, and apoptosis, whereas in bladder and squamous cell carcinoma, it interferes with EGFR-related signaling and lectin-mediated interactions. It selectively kills liver cancer cells through intracellular Na⁺ overload and mitochondrial damage, and in thyroid cancer, it disrupts cellular respiration and AMPK/mTOR signaling. In glioblastoma, it exhibits both anti-tumor and anti-angiogenic effects, while in hematologic malignancies such as leukemia and lymphoma, it induces apoptosis, cell-cycle arrest, and glycosylation alterations. Collectively, these findings highlight monensin as a highly promising, broad-spectrum anticancer candidate. Its multifaceted mechanisms of action and consistent efficacy across diverse tumor types provide a compelling rationale for continued preclinical evaluation and potential clinical translation. These insights position monensin as an innovative therapeutic avenue, offering new hope for the development of versatile and effective cancer treatments.
Insights
Monensin, a veterinary drug, shows broad-spectrum anticancer potential by selectively killing diverse cancer cells. Preclinical studies reveal its effectiveness against various malignancies, including breast, prostate, and liver cancers.
Area of Science:
- Oncology
- Pharmacology
- Veterinary Medicine
Background:
- Monensin, a polyether ionophore, is widely used in veterinary medicine.
- Emerging evidence suggests monensin possesses multimodal anticancer properties.
Purpose of the Study:
- To provide a comprehensive overview of preclinical studies on monensin's anticancer effects.
- To explore monensin's efficacy and mechanisms across various cancer types.
Main Methods:
- Review of preclinical studies investigating monensin's effects on cancer cells.
- Analysis of monensin's impact on proliferation, apoptosis, signaling pathways, and cellular processes in diverse malignancies.
Main Results:
- Monensin demonstrates selective cytotoxic and anti-progression effects in breast, prostate, pancreatic, ovarian, cervical, renal, bladder, squamous cell, liver, thyroid, glioblastoma, leukemia, and lymphoma models.
- Mechanisms include apoptosis induction, cell-cycle arrest, disruption of signaling pathways (e.g., EGFR, androgen receptor, AMPK/mTOR), mitochondrial damage, and glycosylation alterations.
Conclusions:
- Monensin is a promising broad-spectrum anticancer candidate with multifaceted mechanisms of action.
- Consistent efficacy across diverse tumor types warrants continued preclinical evaluation and potential clinical translation for novel cancer treatments.
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