Evidence map›Paper›PMID 42340491›Full record

ArticleMolecular biology reports2026

Synergistic inhibitory effects of combined liposomal formulations of caffeic acid phenethyl ester and vitamin D on melanoma cell proliferation.

Azita Bahrami, Leila Zolghadr, Alireza Farasat, Nematollah Gheibi

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Article in Molecular biology reports, 2026. 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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5 · Who and what money

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4 authors.

Azita BahramiCellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Islamic Republic of Iran. azita.bahrami.1365@gmail.com.ORCID http://orcid.org/0000-0002-7863-2812
Leila ZolghadrDepartment of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Islamic Republic of Iran.ORCID http://orcid.org/0000-0001-5220-1048
Alireza FarasatMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Islamic Republic of Iran.ORCID http://orcid.org/0000-0002-4303-1101
Nematollah GheibiCellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Islamic Republic of Iran. gheibi_n@yahoo.com.ORCID http://orcid.org/0000-0001-7503-0894

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundcaffeic acid phenethyl ester (CAPE) and vitamin D inhibit melanoma growth through various anti-tumor mechanisms. The study investigated the impact of a 1:1 molar ratio of CAPE/vitamin D, both in free and liposomal forms, on inducing cytotoxicity in A375 and B16F10 melanoma cell lines, as well as HDF-1 normal human dermal fibroblasts.

methodsThe physical characteristics of liposomal CAPE/vitamin D prepared by thin-film hydration were analyzed. The cytotoxicity of CAPE and vitamin D combination, in free and liposomal forms, was assessed using the MTT assay, along with their synergy or antagonism analysis. CalcuSyn software was used to calculate the combination index, and the impact of both free and liposomal forms of CAPE/vitamin D on apoptosis and necrosis was examined. Nanomechanical properties and PI3K/AKT1 and BAX/BCL2 gene expression levels were also assessed.

resultsThe highest drug release from nanoliposomes was recorded at 88.12% for CAPE and 76.39% for vitamin D in pH = 5.5. The encapsulation efficiency of CAPE and vitamin D within liposomes was found to be 81.04% and 72.35%, respectively. The IC50 values for A375, B16F10 and HDF-1 cells exposed to liposomal formulations were 8.74 µg/mL, 13.36 µg/mL and 32.49 µg/mL, respectively, after 48 h, while cells incubated with a free mixture of CAPE and vitamin D had IC50 values of 18.31 µg/mL, 24.53 µg/mL and 40.68 µg/mL, respectively. Liposomal CAPE/vitamin D induced more apoptosis in cells than the free mixture, caused nanomechanical changes, and reduced the expression ratio of PI3K to AKT1 genes.

conclusionLiposomes containing CAPE and vitamin D in a 1:1 molar ratio were more effective in inducing A375, B16F10 and HDF-1 cells death compared to their free mixture.

Indexed as

Caffeic AcidsMelanomaPhenylethyl AlcoholVitamin DAnimalsApoptosisCell Line, TumorCell ProliferationDrug SynergismHumansLiposomesMicecaffeic acid phenethyl esterCaffeic AcidsLiposomesPhenylethyl AlcoholVitamin DApoptosisCAPELiposomesMelanoma cancerSynergismVitamin D

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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.