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Yes-activated protein promotes primary resistance of BRAF V600E mutant metastatic colorectal cancer cells to mitogen-activated protein kinase pathway inhibitors

https://doi.org/10.21037/jgo-21-258
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ijc.31220openalex-snapshot
Palbociclib synergizes with BRAF and MEK inhibitors in treatment naïve melanoma but not after the development of BRAF inhibitor resistance
inferredcites →https://doi.org/10.1002/jcb.27808openalex-snapshot
Signal transducer and activator of transcription 3 inhibition enhances vemurafenib sensitivity in colon cancers harboring the BRAFV600E mutation
inferredcites →https://doi.org/10.1002/jcp.25850openalex-snapshot
The SGK1 inhibitor SI113 induces autophagy, apoptosis, and endoplasmic reticulum stress in endometrial cancer cells
inferredcites →https://doi.org/10.1016/j.bbrc.2017.06.092openalex-snapshot
The novel YAP target gene, SGK1, upregulates TAZ activity by blocking GSK3β-mediated TAZ destabilization
inferredcites →https://doi.org/10.1016/j.biopha.2019.108967openalex-snapshot
Qing Chang Hua Shi granule ameliorate inflammation in experimental rats and cell model of ulcerative colitis through MEK/ERK signaling pathway
inferredcites →https://doi.org/10.1016/j.canlet.2016.02.045openalex-snapshot
Nuclear accumulation of Yes-Associated Protein (YAP) maintains the survival of doxorubicin-induced senescent cells by promoting survivin expression
inferredcites →https://doi.org/10.1016/j.canlet.2017.05.015openalex-snapshot
A combinatorial strategy using YAP and pan-RAF inhibitors for treating KRAS-mutant pancreatic cancer
inferredcites →https://doi.org/10.1016/j.canlet.2017.05.017openalex-snapshot
Targeting of super-enhancers and mutant BRAF can suppress growth of BRAF -mutant colon cancer cells via repression of MAPK signaling pathway
inferredcites →https://doi.org/10.1016/j.ccell.2018.11.006openalex-snapshot
Loss of the FAT1 Tumor Suppressor Promotes Resistance to CDK4/6 Inhibitors via the Hippo Pathway
inferredcites →https://doi.org/10.1016/j.celrep.2015.03.015openalex-snapshot
Transcriptional Co-repressor Function of the Hippo Pathway Transducers YAP and TAZ
inferredcites →https://doi.org/10.1016/j.jhep.2009.02.027openalex-snapshot
Protein kinase SGK1 enhances MEK/ERK complex formation through the phosphorylation of ERK2: Implication for the positive regulatory role of SGK1 on the ERK function during liver regeneration
inferredcites →https://doi.org/10.1016/j.tranon.2020.100795openalex-snapshot
Encorafenib, Binimetinib, and Cetuximab in BRAF V600E-Mutated Colorectal Cancer
inferredcites →https://doi.org/10.1038/nature10868openalex-snapshot
Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR
inferredcites →https://doi.org/10.1038/ng.3218openalex-snapshot
The Hippo effector YAP promotes resistance to RAF- and MEK-targeted cancer therapies
inferredcites →https://doi.org/10.1038/onc.2017.120openalex-snapshot
Oncogenic KRAS-associated gene signature defines co-targeting of CDK4/6 and MEK as a viable therapeutic strategy in colorectal cancer
inferredcites →https://doi.org/10.1038/onc.2017.384openalex-snapshot
RAF inhibitor LY3009120 sensitizes RAS or BRAF mutant cancer to CDK4/6 inhibition by abemaciclib via superior inhibition of phospho-RB and suppression of cyclin D1
inferredcites →https://doi.org/10.1038/s41419-018-0698-3openalex-snapshot
miR-550a-3-5p acts as a tumor suppressor and reverses BRAF inhibitor resistance through the direct targeting of YAP
inferredcites →https://doi.org/10.1042/bj20141005openalex-snapshot
Hepatic serum- and glucocorticoid-regulated protein kinase 1 (SGK1) regulates insulin sensitivity in mice via extracellular-signal-regulated kinase 1/2 (ERK1/2)
inferredcites →https://doi.org/10.1056/nejmoa1908075openalex-snapshot
Encorafenib, Binimetinib, and Cetuximab in BRAF V600E–Mutated Colorectal Cancer
inferredcites →https://doi.org/10.1074/jbc.rev119.007963openalex-snapshot
Control of cellular responses to mechanical cues through YAP/TAZ regulation
inferredcites →https://doi.org/10.1080/15384101.2015.1032644openalex-snapshot
YAP in MAPK pathway targeted therapy resistance
inferredcites →https://doi.org/10.1080/23723556.2015.1021441openalex-snapshot
The Hippo effector YAP regulates the response of cancer cells to MAPK pathway inhibitors
inferredcites →https://doi.org/10.1111/pcmr.12211openalex-snapshot
Cyclin‐dependent kinases as therapeutic targets in melanoma
inferredcites →https://doi.org/10.1111/pcmr.12742openalex-snapshot
Inhibition of isoprenylation synergizes with MAPK blockade to prevent growth in treatment‐resistant melanoma, colorectal, and lung cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-12-3793openalex-snapshot
YAP/TEAD–Mediated Transcription Controls Cellular Senescence
inferredcites →https://doi.org/10.1158/0008-5472.can-17-1767openalex-snapshot
miR-6883 Family miRNAs Target CDK4/6 to Induce G1 Phase Cell-Cycle Arrest in Colon Cancer Cells
inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-0665openalex-snapshot
Apoptosis Induction in Human Melanoma Cells by Inhibition of MEK Is Caspase-Independent and Mediated by the Bcl-2 Family Members PUMA, Bim, and Mcl-1
inferredcites →https://doi.org/10.1158/1541-7786.mcr-17-0404openalex-snapshot
Targeting CDK1 and MEK/ERK Overcomes Apoptotic Resistance in BRAF-Mutant Human Colorectal Cancer
inferredcites →https://doi.org/10.1158/2159-8290.cd-17-1226openalex-snapshot
Combined BRAF, EGFR, and MEK Inhibition in Patients with BRAF V600E-Mutant Colorectal Cancer
inferredcites →https://doi.org/10.1158/2159-8290.cd-18-0125openalex-snapshot
Advances on the BRAF Front in Colorectal Cancer
inferredcites →https://doi.org/10.1158/2159-8290.cd-18-0224openalex-snapshot
Dual MAPK/CDK Targeting in Melanoma: New Approaches, New Challenges
inferredcites →https://doi.org/10.1159/000354486openalex-snapshot
Inhibition of Colonic Tumor Growth by the Selective SGK Inhibitor EMD638683
inferredcites →https://doi.org/10.15252/embj.201593584openalex-snapshot
Eradicating tumor drug resistance at its YAP‐biomechanical roots
inferredcites →https://doi.org/10.3322/caac.21387openalex-snapshot
Cancer statistics, 2017
inferredcites →https://doi.org/10.3322/caac.21395openalex-snapshot
Colorectal cancer statistics, 2017
inferredcites →https://doi.org/10.3390/ijms18071527openalex-snapshot
Role Played by Signalling Pathways in Overcoming BRAF Inhibitor Resistance in Melanoma
inferredcites →https://doi.org/10.3748/wjg.v21.i20.6180openalex-snapshot
SGK1 inhibits cellular apoptosis and promotes proliferationviathe MEK/ERK/p53 pathway in colitis
inferredcites →https://doi.org/10.3892/or.2018.6630openalex-snapshot
Inhibition of YAP reverses primary resistance to EGFR inhibitors in colorectal cancer cells
inferredcites →https://doi.org/10.5483/bmbrep.2018.51.3.018openalex-snapshot
Clinical implications of the Hippo-YAP pathway in multiple cancer contexts

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3940635openalex-extracted
Capicua Suppresses YAP1 To Limit Tumorigenesis and Maintain Drug Sensitivity in Human Cancer
inferred← citeshttps://doi.org/10.1002/jcb.30517openalex-snapshot
The rational modulation of autophagy sensitizes colorectal cancer cells to 5‐fluouracil and oxaliplatin
inferred← citeshttps://doi.org/10.1007/s44371-026-00562-3openalex-snapshot
Dual targeting of YAP1 and β-catenin: a therapeutic strategy for colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111443openalex-snapshot
Capicua suppresses YAP1 to limit tumorigenesis and maintain drug sensitivity in human cancer
inferred← citeshttps://doi.org/10.1016/j.drup.2026.101387openalex-snapshot
Programmed cell death network in cancer drug resistance: A framework for therapeutic intervention
inferred← citeshttps://doi.org/10.1038/s41598-023-50443-3openalex-snapshot
Characterization of dabrafenib-induced drug insensitivity via cellular barcoding and collateral sensitivity to second-line therapeutics
inferred← citeshttps://doi.org/10.3390/cancers16050852openalex-snapshot
Identification of a Gene Signature That Predicts Dependence upon YAP/TAZ-TEAD
inferred← citeshttps://doi.org/10.3390/cells10102715openalex-snapshot
Recent Therapeutic Approaches to Modulate the Hippo Pathway in Oncology and Regenerative Medicine
inferred← citeshttps://doi.org/10.3390/pharmaceutics14020391openalex-snapshot
Identification of a Quinone Derivative as a YAP/TEAD Activity Modulator from a Repurposing Library
inferred← citeshttps://doi.org/10.7150/ijbs.83586openalex-snapshot
Role Of YAP Signaling in Regulation of Programmed Cell Death and Drug Resistance in Cancer
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