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BIOMARKER:

CDH2 overexpression + KRAS wild-type

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Other names: CDH2, Cadherin 2, CDHN, Cadherin 2, Type 1, N-Cadherin (Neuronal), Neural Cadherin, N-Cadherin, Cadherin-2, CDw325, CD325, NCAD, Calcium-Dependent Adhesion Protein, Neuronal, CD325 Antigen, N-Cadherin 1, KRAS, KRAS proto-oncogene GTPase, KRAS1, KRAS2, NS, NS3, OES, CFC2, RALD, K-Ras, RASK2, KI-RAS, C-K-RAS, K-RAS2A, K-RAS2B, K-RAS4A, K-RAS4B, K-Ras 2, C-K-RAS, c-Ki-ras, c-Ki-ras2, Kirsten rat sarcoma viral oncogene homolog
Entrez ID:
Related biomarkers:
1year
N-Cadherin acts as a predictive biomarker for anti-FGFR therapy in KRAS wild-type NSCLC (AACR 2023)
Therefore, it is essential the identification of new biomarkers that could help to predict more accurately those patients that could benefit from anti-FGFR therapy.Materials and We have treated 15 NSCLC PDX models with high FGFR1 expression levels and variable N-Cadherin expression levels, with the FGFR inhibitor (FGFRi) AZD4547... In conclusion, previous research had underlined N-Cadherin as a potential biomarker of response to FGFRi, while not successful in all contexts. Transcriptome study of PDXs classified as responder or non-responder to FGFRi revealed a differential gene expression pattern, with an upregulation of N-Cadherin pathway observed in the Responder group, while an enrichment of KRAS signaling and KRAS mutations in non-Responders. Furthermore, we validated our finding using a cell line repository that confirm that N-Cadherin could predict FGFR-targeted therapy efficacy but only in the KRAS wildtype context .
KRAS (KRAS proto-oncogene GTPase) • FGFR (Fibroblast Growth Factor Receptor) • CDH2 (Cadherin 2)
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KRAS mutation • FGFR1 amplification • KRAS wild-type • RAS wild-type • FGFR1 expression • CDH1 expression • CDH2 overexpression + KRAS wild-type • KRAS expression
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fexagratinib (ABSK091)