| Literature DB >> 29577418 |
Marie-Charlotte Brüggen1,2, Joanna Mangana1,2, Anja Irmisch1,2, Lars E French1,2, Mitchell P Levesque1,2, Phil F Cheng1,2, Reinhard Dummer1,2.
Abstract
Methadone (Met) mainly acts as a μ-opioid receptor agonist. Recent evidence pointing towards the role of Met in sensitization of certain cancer cell lines to chemotherapeutic agents has promoted the hypothesis that Met may be a useful adjuvant to cancer chemotherapy. We wanted to address whether Met has, alone or in combination with a chemotherapeutic agent, an effect on melanoma cell viability in vitro. Only a small fraction (4.3%) of our 102 melanoma biobank cell lines with RNA-sequencing data showed expression of the main receptor for Met (OPRM1). We assessed the viability of melanoma cell lines with high, medium or low/no OPRM1 expression (OPRM1high , OPRM1med , OPRM1neg ) 72 hours after treatment with Met alone or combined with cisplatin (Cis). Our analyses show that Met alone did not affect cell viability. While Cis/Met treatment did not have an effect on viability of OPRM1med or OPRM1neg cell lines, it resulted in a slightly decreased cell viability of OPRM1high cells. Clinically, concurrent temozolomide/Met treatment did not have an effect in our single-case report of a patient suffering from uveal melanoma. Taken together, our findings do not provide evidence for recommending Met as an adjuvant to chemotherapy in patients with melanoma.Entities:
Keywords: OPRM1; cisplatin; melanoma; methadone
Mesh:
Substances:
Year: 2018 PMID: 29577418 DOI: 10.1111/exd.13543
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960