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肽-药物偶联物(PDC)数据库:肽-药物偶联物(PDC)的生物活性与药学信息

PDCdb: the biological activity and pharmaceutical information of peptide-drug conjugate (PDC).

作者信息

Sun Xiuna, Li Hanyang, Chen Zhen, Zhang Yang, Wei Zhangle, Xu Hangwei, Liao Yang, Jiang Wanghao, Ge Yichao, Zheng Lingyan, Li Teng, Wu Yuting, Luo Meiyin, Fang Luo, Dong Xiaowu, Xiao Mang, Han Lianyi, Jia Qingzhong, Zhu Feng

机构信息

School of Pharmacy, Hebei Medical University, Shijiazhuang 050017, China.

College of Pharmaceutical Sciences, Department of Otolaryngology Head and Neck Surgery, Sir Run Run Shaw Hospital, The Second Affiliated Hospital, Zhejiang University School of Medicine, State Key Laboratory of Advanced Drug Delivery and Release Systems, Zhejiang University, Hangzhou 310058, China.

出版信息

Nucleic Acids Res. 2025 Jan 6;53(D1):D1476-D1485. doi: 10.1093/nar/gkae859.

Abstract

Peptide-drug conjugates (PDCs) have emerged as a promising class of targeted therapeutics with substantial pharmaceutical advantages and market potentials, which is a combination of a peptide (selective to the disease-relevant target), a linker (stable in circulation but cleavable at target site) and a cytotoxic/radioactive drug (efficacious/traceable for disease). Among existing PDCs, those based on radiopharmaceuticals (a.k.a. radioactive drugs) are valued due to their accurate imaging and targeted destruction of disease sites. It's demanded to accumulate the biological activity and pharmaceutical information of PDCs. Herein, a database PDCdb was thus constructed to systematically describe these valuable data. Particularly, biological activities for 2036 PDCs were retrieved from literatures, which resulted in 1684, 613 and 2753 activity data generated based on clinical trial, animal model and cell line, respectively. Furthermore, the pharmaceutical information for all 2036 PDCs was collected, which gave the diverse data of (a) ADME property, plasma half-life and administration approach of a PDC and (b) chemical modification, primary target, mode of action, conjugating feature of the constituent peptide/linker/drug. In sum, PDCdb systematically provided the biological activities and pharmaceutical information for the most comprehensive list of PDCs among the available databases, which was expected to attract broad interest from related communities and could be freely accessible at: https://idrblab.org/PDCdb/.

摘要

肽-药物偶联物(PDCs)已成为一类具有巨大药学优势和市场潜力的靶向治疗药物,它是由一种肽(对疾病相关靶点具有选择性)、一个连接子(在循环中稳定但在靶点部位可裂解)和一种细胞毒性/放射性药物(对疾病有效/可追踪)组成的复合物。在现有的PDCs中,基于放射性药物(又称放射性药品)的PDCs因其对疾病部位的精确成像和靶向破坏而受到重视。需要积累PDCs的生物学活性和药学信息。在此,构建了一个数据库PDCdb来系统地描述这些有价值的数据。特别地,从文献中检索了2036种PDCs的生物学活性,分别得到了基于临床试验、动物模型和细胞系产生的1684、613和2753条活性数据。此外,收集了所有2036种PDCs的药学信息,这些信息提供了以下不同的数据:(a)一种PDC的吸收、分布、代谢和排泄特性、血浆半衰期和给药途径,以及(b)化学修饰、主要靶点、作用方式、组成肽/连接子/药物的偶联特征。总之,PDCdb系统地提供了现有数据库中最全面的PDCs列表的生物学活性和药学信息,预计将引起相关领域的广泛关注,可通过以下网址免费访问:https://idrblab.org/PDCdb/

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4487/11701599/1e247b19fd6a/gkae859figgra1.jpg

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