The recombinant anti-MET/EpCAM bispecific antibody fragment: a promising novel therapeutic approach for breast cancer treatment.

IF 2.7 3区 医学 Q2 ONCOLOGY
Investigational New Drugs Pub Date : 2025-06-01 Epub Date: 2025-05-30 DOI:10.1007/s10637-025-01546-3
Roya Mirzaei, Mohammadreza Azimi, Soroush Karimi, Mahshid Seyed Karimi, Seyed Ali Mir Aghel, Malihe Salehi, Neda Jalili, Fatemeh Yadegari, Leila Farahmand
{"title":"The recombinant anti-MET/EpCAM bispecific antibody fragment: a promising novel therapeutic approach for breast cancer treatment.","authors":"Roya Mirzaei, Mohammadreza Azimi, Soroush Karimi, Mahshid Seyed Karimi, Seyed Ali Mir Aghel, Malihe Salehi, Neda Jalili, Fatemeh Yadegari, Leila Farahmand","doi":"10.1007/s10637-025-01546-3","DOIUrl":null,"url":null,"abstract":"<p><p>Our study aims to target Met and EpCAM to inhibit angiogenesis in breast cancer, particularly triple-negative breast cancer (TNBC). We have developed a new bispecific antibody that targets both MET and EpCAM, which are commonly overexpressed in tumor cells. This antibody aims to reduce tumor cell proliferation and spread. After cloning and expressing the anti-Met/EPCAM sequence in Escherichia coli, we confirmed its accuracy through Western blot analysis. Flow cytometry indicated its binding activities to MET and EPCAM on MDA-MB-231 and MCF-7 cell lines. Our antibody showed anti-proliferative potential as indicated by apoptosis and MTT assay, leading to the inhibition of migration and invasion in breast cancer cell lines. After conducting a thorough analysis of cytokine production, we discovered that our bispecific antibody effectively influenced the levels of IL-8 and IL-6. These cytokines play crucial roles in angiogenesis and the progression of breast cancer. These findings indicate that our bispecific antibody holds promise as a potential therapy for triple-negative breast cancer. It has the potential to impede the formation of new blood vessels in tumors, thus restraining their growth and spread.</p>","PeriodicalId":14513,"journal":{"name":"Investigational New Drugs","volume":" ","pages":"687-700"},"PeriodicalIF":2.7000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Investigational New Drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10637-025-01546-3","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Our study aims to target Met and EpCAM to inhibit angiogenesis in breast cancer, particularly triple-negative breast cancer (TNBC). We have developed a new bispecific antibody that targets both MET and EpCAM, which are commonly overexpressed in tumor cells. This antibody aims to reduce tumor cell proliferation and spread. After cloning and expressing the anti-Met/EPCAM sequence in Escherichia coli, we confirmed its accuracy through Western blot analysis. Flow cytometry indicated its binding activities to MET and EPCAM on MDA-MB-231 and MCF-7 cell lines. Our antibody showed anti-proliferative potential as indicated by apoptosis and MTT assay, leading to the inhibition of migration and invasion in breast cancer cell lines. After conducting a thorough analysis of cytokine production, we discovered that our bispecific antibody effectively influenced the levels of IL-8 and IL-6. These cytokines play crucial roles in angiogenesis and the progression of breast cancer. These findings indicate that our bispecific antibody holds promise as a potential therapy for triple-negative breast cancer. It has the potential to impede the formation of new blood vessels in tumors, thus restraining their growth and spread.

重组抗met /EpCAM双特异性抗体片段:一种有前景的乳腺癌治疗新方法。
我们的研究旨在靶向Met和EpCAM抑制乳腺癌,特别是三阴性乳腺癌(TNBC)的血管生成。我们开发了一种新的双特异性抗体,可以同时靶向MET和EpCAM,这两种抗体在肿瘤细胞中普遍过表达。这种抗体旨在减少肿瘤细胞的增殖和扩散。我们克隆并在大肠杆菌中表达了抗met /EPCAM序列,并通过Western blot分析证实了其准确性。流式细胞术显示其在MDA-MB-231和MCF-7细胞系上与MET和EPCAM的结合活性。我们的抗体通过细胞凋亡和MTT实验显示出抗增殖潜能,从而抑制乳腺癌细胞株的迁移和侵袭。在对细胞因子的产生进行彻底的分析后,我们发现我们的双特异性抗体有效地影响了IL-8和IL-6的水平。这些细胞因子在血管生成和乳腺癌进展中起着至关重要的作用。这些发现表明,我们的双特异性抗体有望成为治疗三阴性乳腺癌的潜在疗法。它有可能阻碍肿瘤中新血管的形成,从而抑制肿瘤的生长和扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
×
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