Evaluation of Anti-cancer effect of a Novel Formulation from Umbilical Cord Blood Stem CellDerived Exosomes and Retinoic acid as a potential therapeutic candidate against Malignant Melanoma
type: CreativeWork
description: This study focused on two potential therapeutic modalities with good safety profiles, i.e., Retinoic acid (RA) and Umbilical cord blood stem cell (CBSC)-derived exosomes as an anti-cancer drug. The current in vitro study has evaluated the genotoxicity and cytotoxicity of RA and CBSC-derived exosomes, either alone or combined, on lymphocytes from healthy individuals and melanoma patients and on the CHL-1 and FM55 melanoma cell lines. The optimal doses were identified as 10 µM for RA and 120 µl of 107 particles/ml for CBSC-derived exosomes. Both doses significantly exerted cytotoxic and genotoxic effects on FM55 and CHL-1 melanoma cells compared to lymphocytes from healthy and melanoma patients where both treatments showed genoprotective effect (***p<0.001) against oxidative stress induced by hydrogen peroxide (H2O2) and UVA+B (1.2mW/cm2). Moreover, RA rescued DNA damage caused by oxidative stress in both healthy and melanoma lymphocytes. However, in both melanoma cell lines, RA aggravated the genotoxic effect (***p<0.001). Similar results were observed with the CBSC-derived exosomes treatment (***p<0.001). The combined treatment (10 µM RA + 120 µl of 107 particles/ml CBSC-derived exosomes) synergistically increased observed DNA damage in both melanoma cell lines. Moreover, the findings from Western blotting support the RT-qPCR results and the level of upregulation of Caspase-3, P53 and P21 was slightly higher using Western blotting compared to the RT-qPCR and significant initiation of apoptosis was evident in all treatment groups with downregulation of S100 and Bcl-2, particularly for the combined treatment of RA and CBSC-derived exosomes. Therefore, significant activation of p53-mediated apoptosis was detected in FM55 and CHL1 melanoma cells.
abstract: This study focused on two potential therapeutic modalities with good safety profiles, i.e., Retinoic acid (RA) and Umbilical cord blood stem cell (CBSC)-derived exosomes as an anti-cancer drug. The current in vitro study has evaluated the genotoxicity and cytotoxicity of RA and CBSC-derived exosomes, either alone or combined, on lymphocytes from healthy individuals and melanoma patients and on the CHL-1 and FM55 melanoma cell lines. The optimal doses were identified as 10 µM for RA and 120 µl of 107 particles/ml for CBSC-derived exosomes. Both doses significantly exerted cytotoxic and genotoxic effects on FM55 and CHL-1 melanoma cells compared to lymphocytes from healthy and melanoma patients where both treatments showed genoprotective effect (***p<0.001) against oxidative stress induced by hydrogen peroxide (H2O2) and UVA+B (1.2mW/cm2). Moreover, RA rescued DNA damage caused by oxidative stress in both healthy and melanoma lymphocytes. However, in both melanoma cell lines, RA aggravated the genotoxic effect (***p<0.001). Similar results were observed with the CBSC-derived exosomes treatment (***p<0.001). The combined treatment (10 µM RA + 120 µl of 107 particles/ml CBSC-derived exosomes) synergistically increased observed DNA damage in both melanoma cell lines. Moreover, the findings from Western blotting support the RT-qPCR results and the level of upregulation of Caspase-3, P53 and P21 was slightly higher using Western blotting compared to the RT-qPCR and significant initiation of apoptosis was evident in all treatment groups with downregulation of S100 and Bcl-2, particularly for the combined treatment of RA and CBSC-derived exosomes. Therefore, significant activation of p53-mediated apoptosis was detected in FM55 and CHL1 melanoma cells.
author: Masood, Ayesha
language: en
keywords: Malignant melanoma, Retinol, Umbilical Cord Blood Stem Cell-Derived Exosomes, Skin cancer, Comet assay, Western blotting, RT–qPCR, CCK8 assay, Anti-cancer
date modified: 2026-07-24T01:13:34Z
provider: University of Bradford
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Bradford