A comprehensive review of SHP2 and its role in cancer

MD Asmamaw, XJ Shi, LR Zhang, HM Liu - Cellular Oncology, 2022 - Springer
Src homology 2-containing protein tyrosine phosphatase 2 (SHP2) is a non-receptor protein
tyrosine phosphatase ubiquitously expressed mainly in the cytoplasm of several tissues …

Double-edged roles of protein tyrosine phosphatase SHP2 in cancer and its inhibitors in clinical trials

Y Song, M Zhao, H Zhang, B Yu - Pharmacology & therapeutics, 2022 - Elsevier
Phosphorylation is a reversible post-translational modification regulated by phosphorylase
and dephosphorylase to mediate important cellular events. Src homology-2-containing …

BI-3406, a potent and selective SOS1–KRAS interaction inhibitor, is effective in KRAS-driven cancers through combined MEK inhibition

MH Hofmann, M Gmachl, J Ramharter, F Savarese… - Cancer Discovery, 2021 - AACR
KRAS is the most frequently mutated driver of pancreatic, colorectal, and non–small cell lung
cancers. Direct KRAS blockade has proved challenging, and inhibition of a key downstream …

Strategies targeting protein tyrosine phosphatase SHP2 for cancer therapy

Y Song, S Wang, M Zhao, X Yang… - Journal of medicinal …, 2022 - ACS Publications
The protein tyrosine phosphatase SHP2 encoded by PTPN11 is a promising therapeutic
target for cancer therapy, while the multifaceted roles of SHP2 complicate the drug discovery …

[HTML][HTML] Overcoming resistance to drugs targeting KRASG12C mutation

D Jiao, S Yang - The Innovation, 2020 - cell.com
Activating KRAS mutations are present in 25% of human cancer. Although oncogenic Ras
was deemed" undruggable" in the past, recent efforts led to the development of …

Turn and face the strange: § a new view on phosphatases

M Köhn - ACS central science, 2020 - ACS Publications
Phosphorylation as a post-translational modification is critical for cellular homeostasis.
Kinases and phosphatases regulate phosphorylation levels by adding or removing …

[HTML][HTML] KRAS G12C mutations in NSCLC: from target to resistance

A Addeo, GL Banna, A Friedlaender - Cancers, 2021 - mdpi.com
Simple Summary A better understanding of the role of KRAS and its different mutations has
led to the development of specific small-molecule inhibitors able to target KRAS G12C, an …

Discovery of novel Src homology-2 domain-containing phosphatase 2 and histone deacetylase dual inhibitors with potent antitumor efficacy and enhanced antitumor …

M Liu, S Gao, T Liang, X Qiu, X Yang… - Journal of Medicinal …, 2022 - ACS Publications
Both Src homology-2 domain-containing phosphatase 2 (SHP2) and histone deacetylase
(HDAC) are important oncoproteins and potential immunomodulators. In this study, we first …

Crystallographic landscape of SHP2 provides molecular insights for SHP2 targeted drug discovery

Y Song, X Yang, S Wang, M Zhao… - Medicinal Research …, 2022 - Wiley Online Library
The protein tyrosine phosphatase SHP2 encoded by PTPN11 is a promising therapeutic
target for cancer therapy. The dynamic change of SHP2 between closed and open …

[HTML][HTML] Strategies to overcome drug resistance using SHP2 inhibitors

M Liu, S Gao, RM Elhassan, X Hou, H Fang - Acta Pharmaceutica Sinica B, 2021 - Elsevier
Encoded by PTPN11, the SHP2 (Src homology-2 domain-containing protein tyrosine
phosphatase-2) is widely recognized as a carcinogenic phosphatase. As a promising anti …