A bibliometric analysis of PROTAC from 2001 to 2021

被引:82
作者
Li, Deping [1 ]
Yu, Dongmin [2 ]
Li, Yan [1 ]
Yang, Renze [1 ]
机构
[1] Gannan Med Univ, Dept Pharm, Affiliated Hosp 1, Ganzhou 341000, Peoples R China
[2] Gannan Med Univ, Dept Breast Dis, Affiliated Hosp 1, Comprehens Ctr, Ganzhou 341000, Peoples R China
关键词
Proteolysis targeting chimera (PROTAC); Bibliometric; VOSviewer; CiteSpace; Cancer; TARGETED PROTEIN-DEGRADATION; E3 UBIQUITIN LIGASE; SMALL-MOLECULE PROTACS; SELECTIVE DEGRADATION; ESTROGEN-RECEPTOR; DRUG DISCOVERY; MEDIATED DEGRADATION; INDUCE DEGRADATION; CHIMERAS PROTACS; HIGHLY POTENT;
D O I
10.1016/j.ejmech.2022.114838
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Proteolysis targeting chimera (PROTAC) technology, one of the targeted protein degradation technologies, has drawn marked attention from researchers of both academia and industry in recent years. After over two decades of development, the literature on it has proliferated. In order to better grasp the frontiers and hot spots of PROTAC, this bibliometric analysis was carried out. The articles and reviews regarding PROTAC were culled from the Web of Science Core Collection. General information and the trend of publication outputs, countries/ regions, authors, journals, influential papers, and keywords in this field were visually analyzed using CtieSpace, VOSviewer, or Excel software. As a result, a total of 808 publications were included. The number of papers regarding PROTAC significantly increased yearly. These papers mainly come from 45 countries/regions led by the USA and China. 3886 authors were identified participating in these studies, among which Craig M. Crews had the most significant number and influential articles. Journal of Medicinal Chemistry and European Journal of Medicinal Chemistry are the two journals with the most papers. After analysis, the most influential papers were identified in the area, including highly cited papers, references with citation burst, and high co-citated papers. The most common keywords including cancer, E3 ligase, drug discovery, epigenetic, resistance, and so on, represent the current and developing areas of study. BRDs, androgen receptor (AR), HDACs, estrogen receptor (ER), EGFR, CDKs, and KRAS are the most common targets. At last, frontiers and challenges of PROTAC were discussed through the bibliometric analysis. This paper will be helpful for better understanding the frontiers and hotspots of PROTAC.
引用
收藏
页数:21
相关论文
共 144 条
[1]   Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs [J].
An, Sainan ;
Fu, Liwu .
EBIOMEDICINE, 2018, 36 :553-562
[2]   Developing potent PROTACs tools for selective degradation of HDAC6 protein [J].
An, Zixuan ;
Lv, Wenxing ;
Su, Shang ;
Wu, Wei ;
Rao, Yu .
PROTEIN & CELL, 2019, 10 (08) :606-609
[3]   Solution Conformations Shed Light on PROTAC Cell Permeability [J].
Atilaw, Yoseph ;
Poongavanam, Vasanthanathan ;
Nilsson, Caroline Svensson ;
Duy Nguyen ;
Giese, Anja ;
Meibom, Daniel ;
Erdelyi, Mate ;
Kihlberg, Jan .
ACS MEDICINAL CHEMISTRY LETTERS, 2021, 12 (01) :107-114
[4]   Lysosome-targeting chimaeras for degradation of extracellular proteins [J].
Banik, Steven M. ;
Pedram, Kayvon ;
Wisnovsky, Simon ;
Ahn, Green ;
Riley, Nicholas M. ;
Bertozzi, Carolyn R. .
NATURE, 2020, 584 (7820) :291-+
[5]   Use of PROTACS as molecular probes of angiogenesis [J].
Bargagna-Mohan, P ;
Baek, SH ;
Lee, H ;
Kim, K ;
Mohan, R .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (11) :2724-2727
[6]   Huntingtin-lowering strategies for Huntington's disease [J].
Barker, Roger A. ;
Fujimaki, Motoki ;
Rogers, Priya ;
Rubinsztein, David C. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2020, 29 (10) :1125-1132
[7]   Accumulation of PNPLA3 on lipid droplets is the basis of associated hepatic steatosis [J].
BasuRay, Soumik ;
Wang, Yang ;
Smagris, Eriks ;
Cohen, Jonathan C. ;
Hobbs, Helen H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (19) :9521-9526
[8]   Targeted Degradation of Oncogenic KRASG12C by VHL-Recruiting PROTACs [J].
Bond, Michael J. ;
Chu, Ling ;
Nalawansha, Dhanusha A. ;
Li, Ke ;
Crews, Craig M. .
ACS CENTRAL SCIENCE, 2020, 6 (08) :1367-1375
[9]   Lessons in PROTAC Design from Selective Degradation with a Promiscuous Warhead [J].
Bondeson, Daniel P. ;
Smith, Blake E. ;
Burslem, George M. ;
Buhimschi, Alexandru D. ;
Hines, John ;
Jaime-Figueroa, Saul ;
Wang, Jing ;
Hamman, Brian D. ;
Ishchenko, Alexey ;
Crews, Craig M. .
CELL CHEMICAL BIOLOGY, 2018, 25 (01) :78-+
[10]  
Bondeson DP, 2015, NAT CHEM BIOL, V11, P611, DOI [10.1038/NCHEMBIO.1858, 10.1038/nchembio.1858]