Emerging strategies to target RAS signaling in human cancer therapy
K Chen, Y Zhang, L Qian, P Wang - Journal of hematology & oncology, 2021 - Springer
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common
oncogenes, and around 19% of patients with cancer harbor RAS mutations. Cells harboring …
oncogenes, and around 19% of patients with cancer harbor RAS mutations. Cells harboring …
Genomic complexity of multiple myeloma and its clinical implications
Multiple myeloma (MM) is a genetically complex disease that evolves from pre-malignant
stages, such as monoclonal gammaopathy of undetermined significance and smouldering …
stages, such as monoclonal gammaopathy of undetermined significance and smouldering …
[HTML][HTML] Comprehensive characterization of cancer driver genes and mutations
Identifying molecular cancer drivers is critical for precision oncology. Multiple advanced
algorithms to identify drivers now exist, but systematic attempts to combine and optimize …
algorithms to identify drivers now exist, but systematic attempts to combine and optimize …
Targeting RAS–ERK signalling in cancer: promises and challenges
AA Samatar, PI Poulikakos - Nature reviews Drug discovery, 2014 - nature.com
Abstract The RAS–RAF–MEK–ERK signalling pathway is hyperactivated in a high
percentage of tumours, most frequently owing to activating mutations of the KRAS, NRAS …
percentage of tumours, most frequently owing to activating mutations of the KRAS, NRAS …
MEK1 and MEK2 inhibitors and cancer therapy: the long and winding road
The role of the ERK signalling pathway in cancer is thought to be most prominent in tumours
in which mutations in the receptor tyrosine kinases RAS, BRAF, CRAF, MEK1 or MEK2 drive …
in which mutations in the receptor tyrosine kinases RAS, BRAF, CRAF, MEK1 or MEK2 drive …
Mechanisms of resistance to BRAF and MEK inhibitors and clinical update of US Food and Drug Administration-approved targeted therapy in advanced melanoma
S Kakadia, N Yarlagadda, R Awad… - OncoTargets and …, 2018 - Taylor & Francis
Approximately 50% of melanomas harbor an activating BRAF mutation. Combined BRAF
and MEK inhibitors such as dabrafenib and trametinib, vemurafenib and cobimetinib, and …
and MEK inhibitors such as dabrafenib and trametinib, vemurafenib and cobimetinib, and …
A phase I trial of the MEK inhibitor selumetinib (AZD6244) in pediatric patients with recurrent or refractory low-grade glioma: a Pediatric Brain Tumor Consortium …
A Banerjee, RI Jakacki, A Onar-Thomas, S Wu… - Neuro …, 2017 - academic.oup.com
Background. Activation of the mitogen-activated protein kinase pathway is important for
growth of pediatric low-grade gliomas (LGGs). The aim of this study was to determine the …
growth of pediatric low-grade gliomas (LGGs). The aim of this study was to determine the …
Targeting the MAPK–RAS–RAF signaling pathway in cancer therapy
L Santarpia, SM Lippman… - Expert opinion on …, 2012 - Taylor & Francis
Introduction: The MAPK pathway comprises several key signaling components and
phosphorylation events that play a role in tumorigenesis. These activated kinases transmit …
phosphorylation events that play a role in tumorigenesis. These activated kinases transmit …
The Hippo effector YAP promotes resistance to RAF-and MEK-targeted cancer therapies
L Lin, AJ Sabnis, E Chan, V Olivas, L Cade… - Nature …, 2015 - nature.com
Resistance to RAF-and MEK-targeted therapy is a major clinical challenge,,,. RAF and MEK
inhibitors are initially but only transiently effective in some but not all patients with BRAF …
inhibitors are initially but only transiently effective in some but not all patients with BRAF …
Selumetinib plus docetaxel for KRAS-mutant advanced non-small-cell lung cancer: a randomised, multicentre, placebo-controlled, phase 2 study
PA Jänne, AT Shaw, JR Pereira, G Jeannin… - The lancet …, 2013 - thelancet.com
Background No targeted therapies are available for KRAS-mutant non-small-cell lung
cancer (NSCLC). Selumetinib is an inhibitor of MEK1/MEK2, downstream of KRAS, with …
cancer (NSCLC). Selumetinib is an inhibitor of MEK1/MEK2, downstream of KRAS, with …