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Main Authors: Saleh, Mai A, Masoud, Hassan M M, Habib, Mohamed R, AbdElGhany, Sherif R, Amer, Maggie E, Abouel-Nour, Mohamed Fathy
Format: Artículo científico
Language:en
Published: Scientific reports 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/40940399/
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author Saleh, Mai A
Masoud, Hassan M M
Habib, Mohamed R
AbdElGhany, Sherif R
Amer, Maggie E
Abouel-Nour, Mohamed Fathy
author_facet Saleh, Mai A
Masoud, Hassan M M
Habib, Mohamed R
AbdElGhany, Sherif R
Amer, Maggie E
Abouel-Nour, Mohamed Fathy
Saleh, Mai A
Masoud, Hassan M M
Habib, Mohamed R
AbdElGhany, Sherif R
Amer, Maggie E
Abouel-Nour, Mohamed Fathy
collection PubMed - marine biology
contents Marine-derived peptides from Rapana venosa inhibit breast cancer cell growth through synergistic mechanisms with doxorubicin. Saleh, Mai A Masoud, Hassan M M Habib, Mohamed R AbdElGhany, Sherif R Amer, Maggie E Abouel-Nour, Mohamed Fathy Humans Doxorubicin Breast Neoplasms Animals Drug Synergism Apoptosis Female Cell Proliferation Peptides Gastropoda Cell Line, Tumor MCF-7 Cells Antineoplastic Agents Gene Expression Regulation, Neoplastic Snails Marine natural products are a promising source of novel anticancer agents. This study evaluated the antitumor activity of peptide fractions derived from the marine gastropod Rapana venosa against human breast cancer cell lines MCF-7 (estrogen receptor-positive) and MDA-MB-231 (triple-negative). Peptides were isolated by enzymatic hydrolysis and Fast Protein Liquid Chromatography. All seven isolated fractions were systematically screened against four human cancer cell lines (MCF-7, MDA-MB-231, CaCo-2, and HepG2) to assess cancer type selectivity. Cytotoxicity was assessed using MTT assay, while cell cycle progression and apoptosis were analyzed by flow cytometry. Gene expression changes were examined by RT-qPCR. Two peptide fractions, RV1 and RV2, demonstrated remarkable selectivity for breast cancer cells, exhibiting 25-95-fold higher potency compared to other cancer types. These fractions showed significant dose-dependent cytotoxicity with IC values of 6.887-7.288 μg/ml (RV1) and 4.886-6.268 μg/ml (RV2) against breast cancer cells. Both fractions induced G0/G1 cell cycle arrest and promoted apoptosis through multiple pathways, upregulating pro-apoptotic genes (TP53, AIFM1, CASP3, BAX) and downregulating anti-apoptotic markers (BCL2, miR-155). Most significantly, combination treatments with doxorubicin resulted in remarkable synergistic effects, with RV2 + doxorubicin achieving 78.9% total apoptosis compared to 33.5% with doxorubicin alone. These results indicate that R. venosa-derived peptides exert selective anticancer effects against breast cancer cells through multiple mechanisms. The observed selectivity and synergism with doxorubicin suggest their potential as targeted adjuvant agents in combination chemotherapy. Further structural characterization and in vivo studies are needed to advance their therapeutic development.
format Artículo científico
id pubmed_40940399
institution PubMed
language en
publishDate 2025
publisher Scientific reports
record_format pubmed
spellingShingle Marine-derived peptides from Rapana venosa inhibit breast cancer cell growth through synergistic mechanisms with doxorubicin.
Saleh, Mai A
Masoud, Hassan M M
Habib, Mohamed R
AbdElGhany, Sherif R
Amer, Maggie E
Abouel-Nour, Mohamed Fathy
Humans
Doxorubicin
Breast Neoplasms
Animals
Drug Synergism
Apoptosis
Female
Cell Proliferation
Peptides
Gastropoda
Cell Line, Tumor
MCF-7 Cells
Antineoplastic Agents
Gene Expression Regulation, Neoplastic
Snails
Marine-derived peptides from Rapana venosa inhibit breast cancer cell growth through synergistic mechanisms with doxorubicin. Saleh, Mai A Masoud, Hassan M M Habib, Mohamed R AbdElGhany, Sherif R Amer, Maggie E Abouel-Nour, Mohamed Fathy Humans Doxorubicin Breast Neoplasms Animals Drug Synergism Apoptosis Female Cell Proliferation Peptides Gastropoda Cell Line, Tumor MCF-7 Cells Antineoplastic Agents Gene Expression Regulation, Neoplastic Snails Marine natural products are a promising source of novel anticancer agents. This study evaluated the antitumor activity of peptide fractions derived from the marine gastropod Rapana venosa against human breast cancer cell lines MCF-7 (estrogen receptor-positive) and MDA-MB-231 (triple-negative). Peptides were isolated by enzymatic hydrolysis and Fast Protein Liquid Chromatography. All seven isolated fractions were systematically screened against four human cancer cell lines (MCF-7, MDA-MB-231, CaCo-2, and HepG2) to assess cancer type selectivity. Cytotoxicity was assessed using MTT assay, while cell cycle progression and apoptosis were analyzed by flow cytometry. Gene expression changes were examined by RT-qPCR. Two peptide fractions, RV1 and RV2, demonstrated remarkable selectivity for breast cancer cells, exhibiting 25-95-fold higher potency compared to other cancer types. These fractions showed significant dose-dependent cytotoxicity with IC values of 6.887-7.288 μg/ml (RV1) and 4.886-6.268 μg/ml (RV2) against breast cancer cells. Both fractions induced G0/G1 cell cycle arrest and promoted apoptosis through multiple pathways, upregulating pro-apoptotic genes (TP53, AIFM1, CASP3, BAX) and downregulating anti-apoptotic markers (BCL2, miR-155). Most significantly, combination treatments with doxorubicin resulted in remarkable synergistic effects, with RV2 + doxorubicin achieving 78.9% total apoptosis compared to 33.5% with doxorubicin alone. These results indicate that R. venosa-derived peptides exert selective anticancer effects against breast cancer cells through multiple mechanisms. The observed selectivity and synergism with doxorubicin suggest their potential as targeted adjuvant agents in combination chemotherapy. Further structural characterization and in vivo studies are needed to advance their therapeutic development.
title Marine-derived peptides from Rapana venosa inhibit breast cancer cell growth through synergistic mechanisms with doxorubicin.
topic Humans
Doxorubicin
Breast Neoplasms
Animals
Drug Synergism
Apoptosis
Female
Cell Proliferation
Peptides
Gastropoda
Cell Line, Tumor
MCF-7 Cells
Antineoplastic Agents
Gene Expression Regulation, Neoplastic
Snails
url https://pubmed.ncbi.nlm.nih.gov/40940399/