Varaico: Literature-Extracted Genetic Variants

Gene:MET
Variant:p.M1250T
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MET

NM_000245.4:p.M1250T

Associated Papers

Individualized management strategies for advanced non-small cell lung cancer with EGFR exon 19 deletion and L861Q compound mutations based on circulating tumor DNA monitoring: A case report.

Zhu X et al.

Oncology Letters, 2026

41509005 (PubMed )
Supplement: Supplementary_Data2.pdf

Autoregulation of the MET receptor tyrosine kinase by its intracellular juxtamembrane domain.

Linossi EM et al.

The Biochemical Journal, 2025

Discriminating activating, deactivating and resistance variants in protein kinases.

Singh G et al.

Genome Medicine, 2025

41152984 (PubMed )
Supplement: 13073_2025_1564_MOESM2_ESM.xlsx › Table_S6

On-target toxicity limits the efficacy of CDK11 inhibition against cancers with 1p36 deletions.

Julian L et al.

Biorxiv : the Preprint Server for Biology, 2025

40766692 (PubMed )
Supplement: media-14.xlsx › Table_S14_-_KINOMEscan_data

MET variants with activating N-lobe mutations identified in hereditary papillary renal cell carcinomas still require ligand stimulation.

Guérin C et al.

Molecular Oncology, 2025

STX-721, a Covalent EGFR/HER2 Exon 20 Inhibitor, Utilizes Exon 20-Mutant Dynamic Protein States and Achieves Unique Mutant Selectivity Across Human Cancer Models.

Pagliarini RA et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2025

40465424 (PubMed )
Supplement: ccr-24-3833_supplementary_tables1_suppts1.xlsx › Table_2_-_kinomescan

Dual Disruption of DNA Repair by a Novel CHK2 Inhibitor, ART-446, and Olaparib is a Promising Strategy for Triple-Negative Breast Cancer Therapy.

Kang HJ et al.

Biomolecules & Therapeutics, 2025

40195731 (PubMed )
Supplement: bt-33-3-458-supple.pdf

Expert consensus on the diagnosis and treatment of non-small cell lung cancer with MET alteration.

Feng H et al.

Cancer Biology & Medicine, 2025

MET variants with activating N-lobe mutations identified in hereditary papillary renal cell carcinomas still require ligand stimulation.

Guérin C et al.

Biorxiv : the Preprint Server for Biology, 2025

Image-Based Phenotypic Profiling Enables Rapid and Accurate Assessment of EGFR-Activating Mutations in Tissues from Lung Cancer Patients.

Lei Q et al.

Journal of the American Chemical Society, 2025

39745025 (PubMed )
Supplement: ja4c16528_si_001.pdf

Discovery of MDI-114215: A Potent and Selective LIMK Inhibitor To Treat Fragile X Syndrome.

Baldwin AG et al.

Journal of Medicinal Chemistry, 2025

39711116 (PubMed )
Supplement: jm4c02694_si_002.pdf

Discovery of a Novel Mutant-Selective Epidermal Growth Factor Receptor Inhibitor Using an In Silico Enabled Drug Discovery Platform.

Igawa H et al.

Journal of Medicinal Chemistry, 2024

39666597 (PubMed )
Supplement: jm4c01405_si_001.pdf

Advances in the diagnosis and treatment of MET-variant digestive tract tumors.

Zhang C et al.

World Journal of Gastrointestinal Oncology, 2024

A first-in-class Wiskott-Aldrich syndrome protein activator with antitumor activity in hematologic cancers.

Spriano F et al.

Haematologica, 2024

38899342 (PubMed )
Supplement: 2022_282672_SPRIANO_TABS4_SUPPL.xlsx › Discoverex-KINOMEscan

GLI1 confers resistance to PARP inhibitors by activating the DNA damage repair pathway.

Ikeuchi H et al.

Oncogene, 2024

39095584 (PubMed )
Supplement: 41388_2024_3105_MOESM2_ESM.xlsx › Supplementary_Table_S6

Strain-release alkylation of Asp12 enables mutant selective targeting of K-Ras-G12D.

Zheng Q et al.

Nature Chemical Biology, 2024

38443470 (PubMed )
Supplement: 41589_2024_1565_MOESM1_ESM.pdf

Suppression of Glioblastoma Stem Cell Potency and Tumor Growth via LRRK2 Inhibition.

Park S et al.

International Journal of Stem Cells, 2024

38584542 (PubMed )
Supplement: ijsc-17-3-319-supple.pdf

Activating Point Mutations in the MET Kinase Domain Represent a Unique Molecular Subset of Lung Cancer and Other Malignancies Targetable with MET Inhibitors.

Pecci F et al.

Cancer Discovery, 2024

An ALK2 inhibitor, BLU-782, prevents heterotopic ossification in a mouse model of fibrodysplasia ossificans progressiva.

Davis AJ et al.

Science Translational Medicine, 2024

38809966 (PubMed )
Supplement: scitranslmed.abp8334_data_file_s1.zip › abp8334_data_file_S1.xlsx › fig_S1

Discovery and Preclinical Characterization of BIIB129, a Covalent, Selective, and Brain-Penetrant BTK Inhibitor for the Treatment of Multiple Sclerosis.

Himmelbauer MK et al.

Journal of Medicinal Chemistry, 2024

38712838 (PubMed )
Supplement: jm4c00220_si_003.xlsx › comnpound_25

Conserved regulatory motifs in the juxtamembrane domain and kinase N-lobe revealed through deep mutational scanning of the MET receptor tyrosine kinase domain.

Estevam GO et al.

Biorxiv : the Preprint Server for Biology, 2024

Recording and classifying MET receptor mutations in cancers.

Guérin C et al.

Elife, 2024

Biophysical and structural characterization of the impacts of MET phosphorylation on tepotinib binding.

Grädler U et al.

The Journal of Biological Chemistry, 2023

Discovery of a Potent and Selective CDKL5/GSK3 Chemical Probe That Is Neuroprotective.

Ong HW et al.

Acs Chemical Neuroscience, 2023

37084253 (PubMed )
Supplement: cn3c00135_si_001.pdf

Multiparameter phenotypic screening for endogenous TFEB and TFE3 translocation identifies novel chemical series modulating lysosome function.

Carling PJ et al.

Autophagy, 2023

35786165 (PubMed )
Supplement: KAUP_A_2095834_SM5251.zip › Supplementary_Tables_R7.xlsx › Table_S5_-_KINOMEscan_2

Mutations in the MET tyrosine kinase domain and resistance to tyrosine kinase inhibitors in non-small-cell lung cancer.

Yao Y et al.

Respiratory Research, 2023

SGC-CLK-1: A chemical probe for the Cdc2-like kinases CLK1, CLK2, and CLK4.

Tiek D et al.

Current Research in Chemical Biology, 2023

38009092 (PubMed )
Supplement: NIHMS1942723-supplement-Supplementary_data_2.xlsx › CAF-022

MET Signaling Pathways, Resistance Mechanisms, and Opportunities for Target Therapies.

Rivas S et al.

International Journal of Molecular Sciences, 2022

36430388 (PubMed )
Supplement: ijms-23-13898-s001.zip › ijms-1981646-supplementary.pdf

The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK.

Zhang CS et al.

Nature Metabolism, 2022

36217034 (PubMed )
Supplement: 42255_2022_640_MOESM1_ESM.pdf

Designing Novel BCR-ABL Inhibitors for Chronic Myeloid Leukemia with Improved Cardiac Safety.

Pandrala M et al.

Journal of Medicinal Chemistry, 2022

35944901 (PubMed )
Supplement: jm1c01853_si_003.xlsx › US073-0016151-O_GVW001-01-p-000

Discovery and Characterization of a Novel Series of Chloropyrimidines as Covalent Inhibitors of the Kinase MSK1.

Hall A et al.

Acs Medicinal Chemistry Letters, 2022

35859861 (PubMed )
Supplement: ml2c00134_si_001.pdf

Insight into Targeting Exon20 Insertion Mutations of the Epidermal Growth Factor Receptor with Wild Type-Sparing Inhibitors.

Lategahn J et al.

Journal of Medicinal Chemistry, 2022

35486541 (PubMed )
Supplement: jm1c02080_si_001.pdf

Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I.

Sebai M et al.

Human Mutation, 2022

A new ALK inhibitor overcomes resistance to first- and second-generation inhibitors in NSCLC.

Lu Y et al.

Embo Molecular Medicine, 2022

34845836 (PubMed )
Supplement: EMMM-14-e14296-s001.pdf

Discovery of AS-1763: A Potent, Selective, Noncovalent, and Orally Available Inhibitor of Bruton's Tyrosine Kinase.

Kawahata W et al.

Journal of Medicinal Chemistry, 2021

34529443 (PubMed )
Supplement: jm1c01279_si_001.pdf

Capmatinib for patients with non-small cell lung cancer with MET exon 14 skipping mutations: A review of preclinical and clinical studies.

Wu YL et al.

Cancer Treatment Reviews, 2021

A narrative review of MET inhibitors in non-small cell lung cancer with MET exon 14 skipping mutations.

Santarpia M et al.

Translational Lung Cancer Research, 2021

Oncogenic mechanism-based pharmaceutical validation of therapeutics targeting MET receptor tyrosine kinase.

Yao HP et al.

Therapeutic Advances in Medical Oncology, 2021

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."