噬菌体展示
生物信息学
表皮生长因子受体
免疫原性
体内
癌症
计算生物学
靶向治疗
癌症研究
肽库
肽
生物
抗体
免疫学
生物化学
肽序列
生物技术
基因
遗传学
作者
Mohammad Ahmadi,Yaghoub Ahmadyousefi,Zahra Salimi,Rasoul Mirzaei,Rezvan Najafi,Bagher Amirheidari,Fatemeh Rahbarizadeh,Javad Kheshti,Armin Safari,Meysam Soleimani
出处
期刊:ChemMedChem
[Wiley]
日期:2022-12-05
卷期号:18 (3)
被引量:4
标识
DOI:10.1002/cmdc.202200506
摘要
Abstract 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.
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