[HTML][HTML] Overcoming Immune Checkpoint Therapy Resistance with SHP2 Inhibition in Cancer and Immune Cells: A Review of the Literature and Novel Combinatorial …
Simple Summary This is a thorough literature review of SHP2 inhibition, its application in
cancer therapy and current uses as an immune modulator. The aberrant activation of SHP2 …
cancer therapy and current uses as an immune modulator. The aberrant activation of SHP2 …
[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 …
phosphatase-2) is widely recognized as a carcinogenic phosphatase. As a promising anti …
[HTML][HTML] Tyrosine phosphatase PTPN11/SHP2 in solid tumors - bull's eye for targeted therapy?
X Chen, SJ Keller, P Hafner, AY Alrawashdeh… - Frontiers in …, 2024 - frontiersin.org
Encoded by PTPN11, the Src-homology 2 domain-containing phosphatase 2 (SHP2)
integrates signals from various membrane-bound receptors such as receptor tyrosine …
integrates signals from various membrane-bound receptors such as receptor tyrosine …
Allosteric inhibitors of SHP2 with therapeutic potential for cancer treatment
SHP2, a cytoplasmic protein-tyrosine phosphatase encoded by the PTPN11 gene, is
involved in multiple cell signaling processes including Ras/MAPK and Hippo/YAP pathways …
involved in multiple cell signaling processes including Ras/MAPK and Hippo/YAP pathways …
Assessing cellular target engagement by SHP2 (PTPN11) phosphatase inhibitors
LJ Lambert, C Romero, DJ Sheffler… - JoVE (Journal of …, 2020 - jove.com
The Src-homology 2 (SH2) domain-containing phosphatase 2 (SHP2), encoded by the
PTPN11 proto-oncogene, is a key mediator of receptor tyrosine kinase (RTK)-driven cell …
PTPN11 proto-oncogene, is a key mediator of receptor tyrosine kinase (RTK)-driven cell …
Allosteric SHP2 inhibitors in cancer: Targeting the intersection of RAS, resistance, and the immune microenvironment
The nonreceptor protein tyrosine phosphatase SHP2 (encoded by PTPN11) integrates
growth and differentiation signals from receptor tyrosine kinases (RTKs) into the …
growth and differentiation signals from receptor tyrosine kinases (RTKs) into the …
Targeting SHP2 as a promising strategy for cancer immunotherapy
Q Liu, J Qu, M Zhao, Q Xu, Y Sun - Pharmacological research, 2020 - Elsevier
Src homology-2-containing protein tyrosine phosphatase 2 (SHP2) is a major phosphatase
involved in several cellular processes. In recent years, SHP2 has been the focus of …
involved in several cellular processes. In recent years, SHP2 has been the focus of …
SHP2 Inhibition as a Promising Anti-cancer Therapy: Function in Tumor Cell Signaling and Immune Modulation
J Wang, L Zhang, CA Pratilas… - Journal of Cancer …, 2021 - scientificarchives.com
The protein tyrosine phosphatase SHP2, encoded by PTPN11, functions as a critical signal
transduction regulator and interacts with key signaling molecules in both RAS/ERK and PD …
transduction regulator and interacts with key signaling molecules in both RAS/ERK and PD …
BPI-442096: A potent and selective inhibitor of SHP2 for the treatment of multiple cancers
L Li, B Fu, H Han, Z Sun, X Zhao, X Jv, J Tong, J Zhao… - Cancer Research, 2022 - AACR
Src homology region 2 domain-containing phosphatase-2 (SHP-2) is a key node in the RAS
signaling pathway. Allosteric inhibition of SHP2 phosphatase is a potential therapeutic …
signaling pathway. Allosteric inhibition of SHP2 phosphatase is a potential therapeutic …
SHP-1: the next checkpoint target for cancer immunotherapy?
HA Watson, S Wehenkel, J Matthews… - Biochemical Society …, 2016 - portlandpress.com
The immense power of the immune system is harnessed in healthy individuals by a range of
negative regulatory signals and checkpoints. Manipulating these checkpoints through …
negative regulatory signals and checkpoints. Manipulating these checkpoints through …
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