The pathogenic E139D mutation stabilizes a non-canonical active state of the multi-domain phosphatase SHP2. [PDF]
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Erythrocyte membrane-encapsulated SZF nanocomposites for hyperuricemia therapy. [PDF]
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RAS Mutation-Specific Responses to Paralog- and State-Selective RAS Inhibitors. [PDF]
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A first-in-human phase 1 study of the SHP2 inhibitor BBP-398 in patients with advanced solid tumors. [PDF]
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Targeting SHP2 to reverse immune evasion and resistance to anti-PD-1 therapy in non-small cell lung cancer. [PDF]
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PD-1 suppresses CAR signaling by forming the inhibitory signalosome colocalizing to CAR microclusters. [PDF]
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Antitumor effects of LPM5140276 and its potential combination with SHP2 inhibition in KRAS<sup>G12D</sup>-mutant cancer. [PDF]
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Lung adenocarcinoma with KRAS-Q61H: clinicopathologic features, diagnostics, and the evolving treatment landscape. [PDF]
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Phosphatases in tumor cell immune escape: a perspective based on the camouflage, coercion, cytoprotection. [PDF]
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Crystallographic landscape of SHP2 provides molecular insights for SHP2 targeted drug discovery
Medicinal Research Reviews, 2022AbstractThe protein tyrosine phosphatase SHP2 encoded by PTPN11 is a promising therapeutic target for cancer therapy. The dynamic change of SHP2 between closed and open conformations under either physiological or pathological conditions provides opportunities to design SHP2 inhibitors for treating SHP2‐related diseases. To date, several SHP2 allosteric
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