Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)

The major mortality factor for women globally is breast cancer, and current treatments have several adverse effects. Hesperetin (HSP) is a flavone that occurs naturally with anti-tumor capabilities and has been investigated as a potential treatment for cancer. This study aimed to investigate the cyt...

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Main Authors: Ahmed Mohammed Salman, Esmaeil Babaei, Ahmed Salim Kadhim Al-Khafaji
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-01-01
Series:Journal of Advanced Pharmaceutical Technology & Research
Subjects:
Online Access:http://www.japtr.org/article.asp?issn=2231-4040;year=2024;volume=15;issue=1;spage=43;epage=48;aulast=Salman
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author Ahmed Mohammed Salman
Esmaeil Babaei
Ahmed Salim Kadhim Al-Khafaji
author_facet Ahmed Mohammed Salman
Esmaeil Babaei
Ahmed Salim Kadhim Al-Khafaji
author_sort Ahmed Mohammed Salman
collection DOAJ
description The major mortality factor for women globally is breast cancer, and current treatments have several adverse effects. Hesperetin (HSP) is a flavone that occurs naturally with anti-tumor capabilities and has been investigated as a potential treatment for cancer. This study aimed to investigate the cytotoxic and anti-malignant potential of HSP on breast cancer cells (BT-474) and normal cells (MCF-10a). The results indicated that HSP has dose-dependent cytotoxicity in BT-474 and MCF-10a cells. The elevated concentration of HSP lowered cell viability and proliferation. The half-maximal inhibitory concentration (IC50) of HSP in BT-474 cancer cells after a 48-h exposure was 279.2 μM/ml, while the IC50 in normal cells was 855.4 μM/ml. The cytotoxicity of HSP was more significant in cancer cell lines than in normal cell lines and this aspect presents a favorable factor in utilizing the drug for the treatment of breast cancer. The apoptotic effect of HSP in BT-474 cells was investigated, and it was found that the higher the concentration of HSP more the cells underwent apoptosis. Furthermore, the highest concentration of HSP led to overexpression of the MLH1 and MSH2 genes in both breast cancer and normal cell lines. Overall, our study suggests that HSP has an anticancer effect on breast cancer cell lines, and the effect is concentration dependent.
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spelling doaj.art-82d969b1cfd848b29869a1d13c3998142024-02-22T15:01:05ZengWolters Kluwer Medknow PublicationsJournal of Advanced Pharmaceutical Technology & Research2231-40400976-20942024-01-01151434810.4103/japtr.japtr_279_23Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)Ahmed Mohammed SalmanEsmaeil BabaeiAhmed Salim Kadhim Al-KhafajiThe major mortality factor for women globally is breast cancer, and current treatments have several adverse effects. Hesperetin (HSP) is a flavone that occurs naturally with anti-tumor capabilities and has been investigated as a potential treatment for cancer. This study aimed to investigate the cytotoxic and anti-malignant potential of HSP on breast cancer cells (BT-474) and normal cells (MCF-10a). The results indicated that HSP has dose-dependent cytotoxicity in BT-474 and MCF-10a cells. The elevated concentration of HSP lowered cell viability and proliferation. The half-maximal inhibitory concentration (IC50) of HSP in BT-474 cancer cells after a 48-h exposure was 279.2 μM/ml, while the IC50 in normal cells was 855.4 μM/ml. The cytotoxicity of HSP was more significant in cancer cell lines than in normal cell lines and this aspect presents a favorable factor in utilizing the drug for the treatment of breast cancer. The apoptotic effect of HSP in BT-474 cells was investigated, and it was found that the higher the concentration of HSP more the cells underwent apoptosis. Furthermore, the highest concentration of HSP led to overexpression of the MLH1 and MSH2 genes in both breast cancer and normal cell lines. Overall, our study suggests that HSP has an anticancer effect on breast cancer cell lines, and the effect is concentration dependent.http://www.japtr.org/article.asp?issn=2231-4040;year=2024;volume=15;issue=1;spage=43;epage=48;aulast=Salmanapoptosisbreast cancercytotoxicityflow cytometryhalf-maximal inhibitory concentrationhesperetinmalignancymlh1 gene expressionmsh2 gene expression3-(45-dimethylthiazol-2-yl)-25-diphenyltetrazolium bromide assayreal-time polymerase chain reaction
spellingShingle Ahmed Mohammed Salman
Esmaeil Babaei
Ahmed Salim Kadhim Al-Khafaji
Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
Journal of Advanced Pharmaceutical Technology & Research
apoptosis
breast cancer
cytotoxicity
flow cytometry
half-maximal inhibitory concentration
hesperetin
malignancy
mlh1 gene expression
msh2 gene expression
3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide assay
real-time polymerase chain reaction
title Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
title_full Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
title_fullStr Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
title_full_unstemmed Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
title_short Exploring the modulation of MLH1 and MSH2 gene expression in hesperetin-treated breast cancer cells (BT-474)
title_sort exploring the modulation of mlh1 and msh2 gene expression in hesperetin treated breast cancer cells bt 474
topic apoptosis
breast cancer
cytotoxicity
flow cytometry
half-maximal inhibitory concentration
hesperetin
malignancy
mlh1 gene expression
msh2 gene expression
3-(4
5-dimethylthiazol-2-yl)-2
5-diphenyltetrazolium bromide assay
real-time polymerase chain reaction
url http://www.japtr.org/article.asp?issn=2231-4040;year=2024;volume=15;issue=1;spage=43;epage=48;aulast=Salman
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AT esmaeilbabaei exploringthemodulationofmlh1andmsh2geneexpressioninhesperetintreatedbreastcancercellsbt474
AT ahmedsalimkadhimalkhafaji exploringthemodulationofmlh1andmsh2geneexpressioninhesperetintreatedbreastcancercellsbt474