Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells

Abstract Breast cancer is the second most common type of cancer worldwide and the leading cause of cancer death in women. Dietary bioactive compounds may act at different stages of carcinogenesis, including tumor initiation, promotion, and progression. Spices have been used for thousands of years an...

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Main Authors: Carlos Luan A. Passos, Renata Madureira Polinati, Christian Ferreira, Nathalia Alexia Nascimento dos Santos, Daniel Galinis V. Lima, Jerson Lima da Silva, Eliane Fialho
Format: Article
Language:English
Published: Nature Portfolio 2023-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-40535-5
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author Carlos Luan A. Passos
Renata Madureira Polinati
Christian Ferreira
Nathalia Alexia Nascimento dos Santos
Daniel Galinis V. Lima
Jerson Lima da Silva
Eliane Fialho
author_facet Carlos Luan A. Passos
Renata Madureira Polinati
Christian Ferreira
Nathalia Alexia Nascimento dos Santos
Daniel Galinis V. Lima
Jerson Lima da Silva
Eliane Fialho
author_sort Carlos Luan A. Passos
collection DOAJ
description Abstract Breast cancer is the second most common type of cancer worldwide and the leading cause of cancer death in women. Dietary bioactive compounds may act at different stages of carcinogenesis, including tumor initiation, promotion, and progression. Spices have been used for thousands of years and have many bioactive compounds with chemopreventive and chemotherapeutic properties. Curcumin has a multitude of beneficial biological properties, including anti-inflammatory and anticancer effects. This study investigated the effects of cotreatment with curcumin and the chemotherapeutic drug melphalan in cultured MDA-MB-231 breast cancer cells. When used alone, both curcumin and melphalan had a cytotoxic effect on breast cancer cells. Combined treatment with 11.65 µM of curcumin and 93.95 µM of melphalan (CURC/MEL) reduced cell viability by 28.64% and 72.43% after 24 h and 48 h, respectively. CURC/MEL reduced the number of colony-forming units and increased ROS levels by 1.36-fold. CURC/MEL alter cell cycle progression, induce apoptosis, and upregulate caspases-3, -7, and -9, in MDA-MB-231 cells. Cotreatment with curcumin and melphalan have anti-breast cancer cells effects and represent a promising candidate for clinical testing.
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spelling doaj.art-4d85013fcf734e4890a85f6048eeafa02023-11-19T13:08:36ZengNature PortfolioScientific Reports2045-23222023-08-0113111110.1038/s41598-023-40535-5Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cellsCarlos Luan A. Passos0Renata Madureira Polinati1Christian Ferreira2Nathalia Alexia Nascimento dos Santos3Daniel Galinis V. Lima4Jerson Lima da Silva5Eliane Fialho6Functional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroFunctional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroFunctional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroFunctional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroFunctional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroMedical Biochemistry Institute, Federal University of Rio de JaneiroFunctional Foods Laboratory, Nutrition Institute, Federal University of Rio de JaneiroAbstract Breast cancer is the second most common type of cancer worldwide and the leading cause of cancer death in women. Dietary bioactive compounds may act at different stages of carcinogenesis, including tumor initiation, promotion, and progression. Spices have been used for thousands of years and have many bioactive compounds with chemopreventive and chemotherapeutic properties. Curcumin has a multitude of beneficial biological properties, including anti-inflammatory and anticancer effects. This study investigated the effects of cotreatment with curcumin and the chemotherapeutic drug melphalan in cultured MDA-MB-231 breast cancer cells. When used alone, both curcumin and melphalan had a cytotoxic effect on breast cancer cells. Combined treatment with 11.65 µM of curcumin and 93.95 µM of melphalan (CURC/MEL) reduced cell viability by 28.64% and 72.43% after 24 h and 48 h, respectively. CURC/MEL reduced the number of colony-forming units and increased ROS levels by 1.36-fold. CURC/MEL alter cell cycle progression, induce apoptosis, and upregulate caspases-3, -7, and -9, in MDA-MB-231 cells. Cotreatment with curcumin and melphalan have anti-breast cancer cells effects and represent a promising candidate for clinical testing.https://doi.org/10.1038/s41598-023-40535-5
spellingShingle Carlos Luan A. Passos
Renata Madureira Polinati
Christian Ferreira
Nathalia Alexia Nascimento dos Santos
Daniel Galinis V. Lima
Jerson Lima da Silva
Eliane Fialho
Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
Scientific Reports
title Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
title_full Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
title_fullStr Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
title_full_unstemmed Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
title_short Curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells
title_sort curcumin and melphalan cotreatment induces cell cycle arrest and apoptosis in mda mb 231 breast cancer cells
url https://doi.org/10.1038/s41598-023-40535-5
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