[HTML][HTML] KMT2D deficiency drives lung squamous cell carcinoma and hypersensitivity to RTK-RAS inhibition
Lung squamous cell carcinoma (LUSC) represents a major subtype of lung cancer with
limited treatment options. KMT2D is one of the most frequently mutated genes in LUSC (> …
limited treatment options. KMT2D is one of the most frequently mutated genes in LUSC (> …
A leucine-rich repeat protein provides a SHOC2 the RAS circuit: a structure-function perspective
JJ Kwon, WC Hahn - Molecular and Cellular Biology, 2021 - Taylor & Francis
ABSTRACT SHOC2 is a prototypical leucine-rich repeat protein that promotes downstream
receptor tyrosine kinase (RTK)/RAS signaling and plays important roles in several cellular …
receptor tyrosine kinase (RTK)/RAS signaling and plays important roles in several cellular …
[HTML][HTML] Single-cell transcriptomics reveals opposing roles of Shp2 in Myc-driven liver tumor cells and microenvironment
WS Chen, Y Liang, M Zong, JJ Liu, K Kaneko… - Cell reports, 2021 - cell.com
The mechanisms of Myc-driven liver tumorigenesis are inadequately understood. Herein we
show that Myc-driven hepatocellular carcinoma (HCC) is dramatically aggravated in mice …
show that Myc-driven hepatocellular carcinoma (HCC) is dramatically aggravated in mice …
Kinetics of RTK activation determine ERK reactivation and resistance to dual BRAF/MEK inhibition in melanoma
The combination of BRAF and MEK inhibitors (BRAFi/MEKi) has shown promising response
rates in treating BRAF-mutant melanoma by inhibiting ERK activation. However, treatment …
rates in treating BRAF-mutant melanoma by inhibiting ERK activation. However, treatment …
From stem to sternum: the role of shp2 in the skeleton
NR Jensen, RR Kelly, KD Kelly, SK Khoo… - Calcified Tissue …, 2023 - Springer
Src homology-2 domain-containing phosphatase 2 (SHP2) is a ubiquitously expressed
phosphatase that is vital for skeletal development and maintenance of chondrocytes …
phosphatase that is vital for skeletal development and maintenance of chondrocytes …
Overcoming MET-mediated resistance in oncogene-driven NSCLC
N Reischmann, C Schmelas, MÁ Molina-Vila… - Iscience, 2023 - cell.com
This study evaluates the efficacy of combining targeted therapies with MET or SHP2
inhibitors to overcome MET-mediated resistance in different NSCLC subtypes. A prevalence …
inhibitors to overcome MET-mediated resistance in different NSCLC subtypes. A prevalence …
AP1/Fra1 confers resistance to MAPK cascade inhibition in pancreatic cancer
C Schneeweis, S Diersch, Z Hassan, L Krauß… - Cellular and Molecular …, 2023 - Springer
Targeting KRAS downstream signaling remains an important therapeutic approach in
pancreatic cancer. We used primary pancreatic ductal epithelial cells and mouse models …
pancreatic cancer. We used primary pancreatic ductal epithelial cells and mouse models …
[HTML][HTML] Allosteric SHP2 inhibition increases apoptotic dependency on BCL2 and synergizes with venetoclax in FLT3-and KIT-mutant AML
B Popescu, C Stahlhut, TC Tarver, S Wishner… - Cell Reports …, 2023 - cell.com
Mutations in the receptor tyrosine kinases (RTKs) FLT3 and KIT are frequent and associated
with poor outcomes in acute myeloid leukemia (AML). Although selective FLT3 inhibitors …
with poor outcomes in acute myeloid leukemia (AML). Although selective FLT3 inhibitors …
[引用][C] Overcoming MET-mediated resistance in oncogene-driven NSCLC
C Schmelas, M Angel, C Esdar, J Albers… - europepmc.org
This study evaluates the efficacy of combining targeted therapies with MET or SHP2
inhibitors to overcome MET-mediated resistance in different NSCLC subtypes. A prevalence …
inhibitors to overcome MET-mediated resistance in different NSCLC subtypes. A prevalence …