A review of recombinant HER3 affibodies with an effective diagnostic view of cancer cells.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2025-03-01 Epub Date: 2024-11-21 DOI:10.1080/1061186X.2024.2420202
Sahar Babaei Khorzoughi, Mehrnoosh Tavakoli, Mojtaba Mortazavi, Zahra Jafarnejad, Abdorrasoul Malekpour, Tara Kopaiee Malek, Farzane Kargar
{"title":"A review of recombinant HER3 affibodies with an effective diagnostic view of cancer cells.","authors":"Sahar Babaei Khorzoughi, Mehrnoosh Tavakoli, Mojtaba Mortazavi, Zahra Jafarnejad, Abdorrasoul Malekpour, Tara Kopaiee Malek, Farzane Kargar","doi":"10.1080/1061186X.2024.2420202","DOIUrl":null,"url":null,"abstract":"<p><p>Breast cancer is one of the leading causes of cancer-related deaths among women globally. Factors like increased expression of HER family members contribute to its development, with elevated HER3 levels-especially in conjunction with tyrosine kinase receptors like HER2-playing a critical role in activating cancer pathways essential for cell survival and proliferation. Detecting high HER3 levels is vital for effective treatment. Affibody proteins, a class that includes antibodies, are used to identify elevated HER3 expression due to their high binding affinity. These innovative non-immune probes show promise in therapy, diagnostics, and biotechnology because of their exceptional specificity and affinity for target proteins. The design of recombinant affibodies enhances HER3 detection accuracy and supports the development of targeted therapies. Advanced engineering techniques optimize these affibodies for stability and binding efficacy, making them suitable for clinical applications. Additionally, their versatility allows integration with imaging technologies for real-time monitoring of HER3 expression and therapeutic responses. This comprehensive approach could lead to more personalized treatment options for patients with HER3-positive breast cancers, improving patient management and outcomes. This study presents recombinant affibodies designed to bind HER3 for cancer cell identification and introduces novel methods for producing various affibody molecules.</p>","PeriodicalId":15573,"journal":{"name":"Journal of Drug Targeting","volume":" ","pages":"316-327"},"PeriodicalIF":4.3000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Drug Targeting","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/1061186X.2024.2420202","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Breast cancer is one of the leading causes of cancer-related deaths among women globally. Factors like increased expression of HER family members contribute to its development, with elevated HER3 levels-especially in conjunction with tyrosine kinase receptors like HER2-playing a critical role in activating cancer pathways essential for cell survival and proliferation. Detecting high HER3 levels is vital for effective treatment. Affibody proteins, a class that includes antibodies, are used to identify elevated HER3 expression due to their high binding affinity. These innovative non-immune probes show promise in therapy, diagnostics, and biotechnology because of their exceptional specificity and affinity for target proteins. The design of recombinant affibodies enhances HER3 detection accuracy and supports the development of targeted therapies. Advanced engineering techniques optimize these affibodies for stability and binding efficacy, making them suitable for clinical applications. Additionally, their versatility allows integration with imaging technologies for real-time monitoring of HER3 expression and therapeutic responses. This comprehensive approach could lead to more personalized treatment options for patients with HER3-positive breast cancers, improving patient management and outcomes. This study presents recombinant affibodies designed to bind HER3 for cancer cell identification and introduces novel methods for producing various affibody molecules.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
综述重组 HER3 亲和体对癌细胞的有效诊断。
乳腺癌是全球妇女因癌症死亡的最常见原因之一。HER家族成员表达增加等因素可能会导致乳腺癌的发生。HER3 表达的升高,尤其是与其他酪氨酸激酶受体(如 HER2)结合时,在激活对乳腺癌细胞存活和增殖至关重要的癌症通路方面发挥着重要作用。检测高水平的 HER3 对有效治疗癌症至关重要。Affibody 蛋白是包括抗体在内的一类物质,由于其特异的高结合亲和力,可用于检测 HER3 受体的高表达。亲和抗体是一种新型的非免疫探针,由于其特殊的特异性和高目标蛋白亲和力,在治疗、诊断和生物技术领域大有可为。这些重组亲和体的创新设计不仅提高了 HER3 检测的准确性,还促进了靶向治疗策略的开发。通过采用先进的工程技术,这些亲和抗体可以得到优化,从而提高稳定性和结合效力,使其成为临床应用的理想候选药物。此外,基于亲和抗体的系统具有多功能性,有可能与成像技术相结合,实现对 HER3 表达和治疗反应的实时监测。这种多方面的方法最终可为 HER3 阳性乳腺癌患者提供更多个性化的治疗方案,从而在这种具有挑战性的疾病中改善患者的整体管理和治疗效果。本研究介绍了用于癌细胞鉴定的与 HER3 结合的重组亲和体,以及生产一系列亲和体分子的新方法。
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 去求助
来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
期刊最新文献
Interactions and communications in the prostate tumour microenvironment: evolving towards effective cancer therapy. SIRT1: a potential therapeutic target for coronary heart disease combined with anxiety or depression. A review of recombinant HER3 affibodies with an effective diagnostic view of cancer cells. Evaluation of anti-diabetic effects of glimepiride/metformin cocrystal. Overcoming antibiotic resistance: the potential and pitfalls of drug repurposing.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1