TY - JOUR
T1 - Comparison of FDA Approved Kinase Targets to Clinical Trial Ones
T2 - Insights from Their System Profiles and Drug-Target Interaction Networks
AU - Xu, Jingyu
AU - Wang, Panpan
AU - Yang, Hong
AU - Zhou, Jin
AU - Li, Yinghong
AU - Li, Xiaoxu
AU - Xue, Weiwei
AU - Yu, Chunyan
AU - Tian, Yubin
AU - Zhu, Feng
N1 - Publisher Copyright:
© 2016 Jingyu Xu et al.
PY - 2016
Y1 - 2016
N2 - Kinase is one of the most productive classes of established targets, but the majority of approved drugs against kinase were developed only for cancer. Intensive efforts were therefore exerted for releasing its therapeutic potential by discovering new therapeutic area. Kinases in clinical trial could provide great opportunities for treating various diseases. However, no systematic comparison between system profiles of established targets and those of clinical trial ones was conducted. The reveal of probable difference or shift of trend would help to identify key factors defining druggability of established targets. In this study, a comparative analysis of system profiles of both types of targets was conducted. Consequently, the systems profiles of the majority of clinical trial kinases were identified to be very similar to those of established ones, but percentages of established targets obeying the system profiles appeared to be slightly but consistently higher than those of clinical trial targets. Moreover, a shift of trend in the system profiles from the clinical trial to the established targets was identified, and popular kinase targets were discovered. In sum, this comparative study may help to facilitate the identification of the druggability of established drug targets by their system profiles and drug-target interaction networks.
AB - Kinase is one of the most productive classes of established targets, but the majority of approved drugs against kinase were developed only for cancer. Intensive efforts were therefore exerted for releasing its therapeutic potential by discovering new therapeutic area. Kinases in clinical trial could provide great opportunities for treating various diseases. However, no systematic comparison between system profiles of established targets and those of clinical trial ones was conducted. The reveal of probable difference or shift of trend would help to identify key factors defining druggability of established targets. In this study, a comparative analysis of system profiles of both types of targets was conducted. Consequently, the systems profiles of the majority of clinical trial kinases were identified to be very similar to those of established ones, but percentages of established targets obeying the system profiles appeared to be slightly but consistently higher than those of clinical trial targets. Moreover, a shift of trend in the system profiles from the clinical trial to the established targets was identified, and popular kinase targets were discovered. In sum, this comparative study may help to facilitate the identification of the druggability of established drug targets by their system profiles and drug-target interaction networks.
UR - http://www.scopus.com/inward/record.url?scp=84982170279&partnerID=8YFLogxK
U2 - 10.1155/2016/2509385
DO - 10.1155/2016/2509385
M3 - Article
C2 - 27547755
AN - SCOPUS:84982170279
SN - 2314-6133
VL - 2016
JO - BioMed Research International
JF - BioMed Research International
M1 - 2509385
ER -