Ahmadi Mohammad, Ahmadyousefi Yaghoub, Salimi Zahra, Mirzaei Rasoul, Najafi Rezvan, Amirheidari Bagher, Rahbarizadeh Fatemeh, Kheshti Javad, Safari Armin, Soleimani Meysam
Department of Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Medical Biotechnology, School of Advanced Medical Sciences and Technologies, Hamadan University of Medical Sciences, Hamadan, Iran.
ChemMedChem. 2023 Feb 1;18(3):e202200506. doi: 10.1002/cmdc.202200506. Epub 2022 Dec 5.
Active targeting using biological ligands has emerged as a novel strategy for the targeted delivery of diagnostic agents to tumor cells. Conjugating functional targeting moieties with diagnostic probes can increase their accumulation in tumor cells and tissues, enhancing signal detection and, thus, the sensitivity of diagnosis. Due to their small size, ease of chemical synthesis and site-specific modification, high tissue penetration, low immunogenicity, rapid blood clearance, low cost, and biosafety, peptides offer several advantages over antibodies and proteins in diagnostic applications. Epidermal growth factor receptor (EGFR) is one of the most promising cancer biomarkers for actively targeting diagnostic and therapeutic agents to tumor cells due to its active involvement and overexpression in various cancers. Several peptides for EGFR-targeting have been identified in the last decades, which have been obtained by multiple means including derivation from natural proteins, phage display screening, positional scanning synthetic combinatorial library, and in silico screening. Many studies have used these peptides as a targeting moiety for diagnosing different cancers in vitro, in vivo, and in clinical trials. This review summarizes the progress of EGFR-targeting peptide-based assays in the molecular diagnosis of cancer.
利用生物配体进行主动靶向已成为将诊断剂靶向递送至肿瘤细胞的一种新策略。将功能性靶向部分与诊断探针缀合可增加它们在肿瘤细胞和组织中的积累,增强信号检测,从而提高诊断的灵敏度。由于其尺寸小、易于化学合成和位点特异性修饰、组织穿透力强、免疫原性低、血液清除快、成本低以及生物安全性好,肽在诊断应用中比抗体和蛋白质具有多个优势。表皮生长因子受体(EGFR)因其在多种癌症中的积极参与和过表达,是将诊断和治疗剂主动靶向肿瘤细胞最有前景的癌症生物标志物之一。在过去几十年中已鉴定出几种靶向EGFR的肽,这些肽通过多种方式获得,包括从天然蛋白质衍生、噬菌体展示筛选、位置扫描合成组合文库和计算机筛选。许多研究已将这些肽用作体外、体内和临床试验中诊断不同癌症的靶向部分。本综述总结了基于靶向EGFR肽的检测方法在癌症分子诊断中的进展。