芦丁通过下调ABC转运蛋白、诱导ROS生成和重置氧化还原状态减轻乳腺癌对他莫昔芬的耐药

IF 2.8 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Heba Effat, Aliaa M. Radwan, Marwa Sharaky, Hamed A. Abosharaf
{"title":"芦丁通过下调ABC转运蛋白、诱导ROS生成和重置氧化还原状态减轻乳腺癌对他莫昔芬的耐药","authors":"Heba Effat,&nbsp;Aliaa M. Radwan,&nbsp;Marwa Sharaky,&nbsp;Hamed A. Abosharaf","doi":"10.1002/jbt.70490","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Breast cancer is one of the most lethal cancers in women worldwide. Tamoxifen (TAM), a nonsteroidal antiestrogen, is a highly successful treatment for breast cancer. However, developed resistance to TAM can substantially impair chemotherapy efficacy, resulting in poor prognosis and cancer recurrence. Rutin (RUT) is a dietary flavonoid with potent anticancer activities, however its fundamental mechanisms in the treatment of TAM-resistant breast cancer remain obscure. We used cell viability assay, qPCR, flow cytometric analysis combined with immunoblotting and molecular docking studies to assess the effects of RUT on chemoresistance, ATP-binding cassette transporters (ABC), and redox status resetting in TAM resistant breast cancer cells. Our results revealed that the treatment of resistant LCC2 cells with a combination of TAM and RUT effectively inhibited cell growth and proliferation. RUT reverses the resistance of LCC2 cells to TAM by downregulating the expression of <i>ABCB1, ABCC1, ABCC2</i>, and <i>ABCG2</i> multidrug resistance genes and inducing the production of reactive oxygen species. Further, western blot results exhibited that TAM combined with RUT reduced the expression levels of Nrf2, GCL, GLS, and SLCA711 proteins in LCC2 cells, which was corroborated by molecular docking. TAM and RUT combination may provide a promising treatment pathway to conquer TAM resistance and hence extend the life expectancy in breast cancer patients.</p></div>","PeriodicalId":15151,"journal":{"name":"Journal of Biochemical and Molecular Toxicology","volume":"39 9","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rutin Alleviates Breast Cancer Resistance to Tamoxifen By Downregulating ABC Transporters, Inducing ROS Generation and Resetting Redox Status\",\"authors\":\"Heba Effat,&nbsp;Aliaa M. Radwan,&nbsp;Marwa Sharaky,&nbsp;Hamed A. Abosharaf\",\"doi\":\"10.1002/jbt.70490\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Breast cancer is one of the most lethal cancers in women worldwide. Tamoxifen (TAM), a nonsteroidal antiestrogen, is a highly successful treatment for breast cancer. However, developed resistance to TAM can substantially impair chemotherapy efficacy, resulting in poor prognosis and cancer recurrence. Rutin (RUT) is a dietary flavonoid with potent anticancer activities, however its fundamental mechanisms in the treatment of TAM-resistant breast cancer remain obscure. We used cell viability assay, qPCR, flow cytometric analysis combined with immunoblotting and molecular docking studies to assess the effects of RUT on chemoresistance, ATP-binding cassette transporters (ABC), and redox status resetting in TAM resistant breast cancer cells. Our results revealed that the treatment of resistant LCC2 cells with a combination of TAM and RUT effectively inhibited cell growth and proliferation. RUT reverses the resistance of LCC2 cells to TAM by downregulating the expression of <i>ABCB1, ABCC1, ABCC2</i>, and <i>ABCG2</i> multidrug resistance genes and inducing the production of reactive oxygen species. Further, western blot results exhibited that TAM combined with RUT reduced the expression levels of Nrf2, GCL, GLS, and SLCA711 proteins in LCC2 cells, which was corroborated by molecular docking. TAM and RUT combination may provide a promising treatment pathway to conquer TAM resistance and hence extend the life expectancy in breast cancer patients.</p></div>\",\"PeriodicalId\":15151,\"journal\":{\"name\":\"Journal of Biochemical and Molecular Toxicology\",\"volume\":\"39 9\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Biochemical and Molecular Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jbt.70490\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biochemical and Molecular Toxicology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jbt.70490","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

乳腺癌是全世界女性中最致命的癌症之一。他莫昔芬(TAM)是一种非甾体抗雌激素,是一种非常成功的乳腺癌治疗方法。然而,TAM的耐药会严重影响化疗效果,导致预后不良和癌症复发。芦丁(Rutin, RUT)是一种具有有效抗癌活性的膳食类黄酮,但其治疗tam耐药乳腺癌的基本机制尚不清楚。我们使用细胞活力测定、qPCR、流式细胞分析结合免疫印迹和分子对接研究来评估RUT对TAM耐药乳腺癌细胞的化疗耐药、atp结合盒转运蛋白(ABC)和氧化还原状态重置的影响。我们的研究结果表明,TAM和RUT联合治疗耐药LCC2细胞有效地抑制了细胞的生长和增殖。RUT通过下调ABCB1、ABCC1、ABCC2和ABCG2多药耐药基因的表达,诱导活性氧的产生,逆转LCC2细胞对TAM的耐药。此外,western blot结果显示,TAM联合RUT降低了LCC2细胞中Nrf2、GCL、GLS和SLCA711蛋白的表达水平,这一点通过分子对接得到了证实。TAM与RUT联合治疗可能为克服TAM耐药,延长乳腺癌患者的预期寿命提供了一条有希望的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rutin Alleviates Breast Cancer Resistance to Tamoxifen By Downregulating ABC Transporters, Inducing ROS Generation and Resetting Redox Status

Rutin Alleviates Breast Cancer Resistance to Tamoxifen By Downregulating ABC Transporters, Inducing ROS Generation and Resetting Redox Status

Breast cancer is one of the most lethal cancers in women worldwide. Tamoxifen (TAM), a nonsteroidal antiestrogen, is a highly successful treatment for breast cancer. However, developed resistance to TAM can substantially impair chemotherapy efficacy, resulting in poor prognosis and cancer recurrence. Rutin (RUT) is a dietary flavonoid with potent anticancer activities, however its fundamental mechanisms in the treatment of TAM-resistant breast cancer remain obscure. We used cell viability assay, qPCR, flow cytometric analysis combined with immunoblotting and molecular docking studies to assess the effects of RUT on chemoresistance, ATP-binding cassette transporters (ABC), and redox status resetting in TAM resistant breast cancer cells. Our results revealed that the treatment of resistant LCC2 cells with a combination of TAM and RUT effectively inhibited cell growth and proliferation. RUT reverses the resistance of LCC2 cells to TAM by downregulating the expression of ABCB1, ABCC1, ABCC2, and ABCG2 multidrug resistance genes and inducing the production of reactive oxygen species. Further, western blot results exhibited that TAM combined with RUT reduced the expression levels of Nrf2, GCL, GLS, and SLCA711 proteins in LCC2 cells, which was corroborated by molecular docking. TAM and RUT combination may provide a promising treatment pathway to conquer TAM resistance and hence extend the life expectancy in breast cancer patients.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.80
自引率
2.80%
发文量
277
审稿时长
6-12 weeks
期刊介绍: The Journal of Biochemical and Molecular Toxicology is an international journal that contains original research papers, rapid communications, mini-reviews, and book reviews, all focusing on the molecular mechanisms of action and detoxication of exogenous and endogenous chemicals and toxic agents. The scope includes effects on the organism at all stages of development, on organ systems, tissues, and cells as well as on enzymes, receptors, hormones, and genes. The biochemical and molecular aspects of uptake, transport, storage, excretion, lactivation and detoxication of drugs, agricultural, industrial and environmental chemicals, natural products and food additives are all subjects suitable for publication. Of particular interest are aspects of molecular biology related to biochemical toxicology. These include studies of the expression of genes related to detoxication and activation enzymes, toxicants with modes of action involving effects on nucleic acids, gene expression and protein synthesis, and the toxicity of products derived from biotechnology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信