Evidence map›Paper›PMID 41379470›Full record

ArticleThe Journal of craniofacial surgery

Peppermint ( Mentha piperita ) Essential Oil Induces Dose-Dependent Cytotoxicity in Human Laryngeal Carcinoma Cells (HNO210).

Zeynel Öztürk, Nuray Bayar Muluk, Suat Utku Keskin, Muhammet Volkan Bulbul, Elvin Alaskarov, Cemal Cingi

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Article in The Journal of craniofacial surgery. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Zeynel ÖztürkDepartment of Otorhinolaryngology, Faculty of Medicine, Istanbul Nişantaşi University and Baypark Hospital, Otolaryngology Clinics, Istanbul.
Nuray Bayar MulukDepartment of Otorhinolaryngology, Faculty of Medicine, Kirikkale University, Kirikkale.
Suat Utku KeskinSchool of Medicine, Koc University, Istanbul.
Muhammet Volkan BulbulDepartment of Histology and Embryology, School of Medicine, Agri Ibrahim Cecen University, Agri.
Elvin AlaskarovDepartment of Otorhinolaryngology, School of Medicine, Istanbul Medipol University, Istanbul.
Cemal CingiDepartment of Otorhinolaryngology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe investigated the cytotoxic effects of Mentha piperita oil on HNO210 human laryngeal cancer cells.

methodsEvery experiment used BHC11100312, BioHippo, cryopreserved HNO210 human laryngeal cancer cells. The cells were cultured in a specific medium containing fetal bovine serum (10%; ATCC 30-2020™) and an antibiotic-antimycotic solution (1%; Gibco, 15240062). Mentha piperita oil was serially diluted to prepare solutions at final concentrations of 10, 50, 100, 150, 200, 250, and 500 µg/mL. The colorimetric MTT assay (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) was used to assess the antiproliferative effects.

resultsA reduction in cell viability was observed after 24 hours of treatment with Mentha piperita oil, and this reduction was dose-dependent. At concentrations above 200 µg/mL, there was a clear cytotoxic response, with cell survival becoming nearly nonexistent. The growth and metabolic stability of HNO210 cells are significantly suppressed by M. piperita oil in vitro. The essential oil of Mentha piperita exhibits a strong cytotoxic effect on HNO210 cells, decreasing their metabolic activity and ability to proliferate after 24 hours of exposure. The treated cells showed obvious signs of cytoplasmic shrinkage, reduced cell density, and loss of intercellular connections. Membrane blebbing and partial detachment from the culture surface were also observed in the treated cultures, indicating cytotoxic stress and potential apoptotic events.

conclusionsMentha piperita oil inhibits the vitality of HNO210 laryngeal cancer cells. It exhibits anticancer potential and has a concentration-dependent cytotoxic effect. The antiproliferative properties of Mentha piperita oil make it a promising candidate for developing effective cancer treatments.

Indexed as

Laryngeal NeoplasmsMentha piperitaOils, VolatilePlant OilsCell Line, TumorCell ProliferationCell SurvivalColorimetryDose-Response Relationship, DrugHumansOils, Volatilepeppermint oilPlant OilsCell morphologycell viabilitycytotoxic effectlaryngeal carcinoma cellsMentha piperita oilMTT assay

Identifiers

PMID41379470
PMCPMC13290042

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.