Targeting receptor tyrosine kinase MET in cancer: small molecule inhibitors and clinical progress

JJ Cui - Journal of medicinal chemistry, 2014 - ACS Publications
The HGF/MET signaling pathway is critical in mediating a wide range of normal physiological
functions including embryological development, wound healing, and tissue regeneration. …

Reprogramming the tumor microenvironment by genome editing for precision cancer therapy

K Liu, JJ Cui, Y Zhan, QY Ouyang, QS Lu, DH Yang… - Molecular Cancer, 2022 - Springer
The tumor microenvironment (TME) is essential for immune escape by tumor cells. It plays
essential roles in tumor development and metastasis. The clinical outcomes of tumors are …

Advanced space-based solar observatory (ASO-S): an overview

…, J Wu, L Deng, Y Huang, JF Yang, JJ Cui… - … in Astronomy and …, 2019 - iopscience.iop.org
The Advanced Space-based Solar Observatory (ASO-S) is a mission proposed for the 25th
solar maximum by the Chinese solar community. The scientific objectives are to study the …

Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal–epithelial transition factor (c-MET) kinase and …

JJ Cui, M Tran-Dubé, H Shen, M Nambu… - Journal of medicinal …, 2011 - ACS Publications
Because of the critical roles of aberrant signaling in cancer, both c-MET and ALK receptor
tyrosine kinases are attractive oncology targets for therapeutic intervention. The cocrystal …

An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms

…, S Yamazaki, TB Koudriakova, G Alton, JJ Cui… - Cancer research, 2007 - AACR
The c-Met receptor tyrosine kinase and its ligand, hepatocyte growth factor (HGF), have
been implicated in the progression of several human cancers and are attractive therapeutic …

A Selective Small Molecule Inhibitor of c-Met Kinase Inhibits c-Met-Dependent Phenotypes in Vitro and Exhibits Cytoreductive Antitumor Activity in Vivo

…, R Blake, KE Lipson, J Ramphal, S Do, JJ Cui… - Cancer research, 2003 - AACR
The c-Met receptor tyrosine kinase and its ligand, hepatocyte growth factor (HGF), have
been implicated in the development and progression of several human cancers and are …

Discovery of (10R)-7-Amino-12-fluoro-2,10,16-trimethyl-15-oxo-10,15,16,17-tetrahydro-2H-8,4-(metheno)pyrazolo[4,3-h][2,5,11]-benzoxadiazacyclotetradecine-3 …

…, A Brooun, BJ Burke, MR Collins, JJ Cui… - Journal of medicinal …, 2014 - ACS Publications
Although crizotinib demonstrates robust efficacy in anaplastic lymphoma kinase (ALK)-positive
non-small-cell lung carcinoma patients, progression during treatment eventually develops…

Repotrectinib (TPX-0005) is a next-generation ROS1/TRK/ALK inhibitor that potently inhibits ROS1/TRK/ALK solvent-front mutations

…, S Stopatschinskaja, DM Hyman, RC Doebele, JJ Cui… - Cancer discovery, 2018 - AACR
JJ Cui has ownership interest (including stock, patents, etc.) in TP Therapeutics, Inc. AT
Shaw is a consultant/advisory board member for member for TP Therapeutics, Pfizer, Blueprint …

Azvudine is a thymus-homing anti-SARS-CoV-2 drug effective in treating COVID-19 patients

…, FM Shao, K Wang, N Sheng, R Li, JJ Cui… - … and Targeted Therapy, 2021 - nature.com
Azvudine (FNC) is a nucleoside analog that inhibits HIV-1 RNA-dependent RNA polymerase
(RdRp). Recently, we discovered FNC an agent against SARS-CoV-2, and have taken it …

Heterogeneity of proangiogenic features in mesenchymal stem cells derived from bone marrow, adipose tissue, umbilical cord, and placenta

WJ Du, Y Chi, ZX Yang, ZJ Li, JJ Cui, BQ Song… - Stem cell research & …, 2016 - Springer
Background Mesenchymal stem cells (MSCs) have been widely proven effective for therapeutic
angiogenesis in ischemia animal models as well as clinical vascular diseases. Because …