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Acquired resistance to imatinib and secondary KIT exon 13 mutation in gastrointestinal stromal tumour
- Source :
- ResearcherID
- Publication Year :
- 2006
- Publisher :
- Spandidos Publications, 2006.
-
Abstract
- Gastrointestinal stromal tumours (GISTs) are the most common mesenchymal tumours of the gastrointestinal tract. Most of them have an activating mutation of KIT or PDGFRalpha tyrosine-kinase receptors. Imatinib is a selective tyrosine-kinase inhibitor of ABL, KIT and PDGFR, and provides a clinical benefit in about 85% of patients with advanced GIST. Unfortunately, secondary resistance following initial responses occurs in most of the cases, and molecular mechanisms are poorly understood. We sequenced KIT and PGDFRalpha exons from one patient with GIST before and after the development of imatinib resistance. We identified, in addition to a primary mutation in exon 9, a secondary mutation in KIT exon 13 (first kinase domain) in the resistant sample. We demonstrate for the first time the feasibility of sequencing such samples removed by non-surgical biopsies during imatinib therapy. Such a approach, far less invasive than surgery and combined with sequencing, will likely help in better tailoring the treatment of advanced GISTs and understanding the mechanisms of resistance and response to imatinib.
- Subjects :
- Cancer Research
Biopsy
Antineoplastic Agents
Biology
Piperazines
Receptor, Platelet-Derived Growth Factor beta
Exon
medicine
Humans
neoplasms
Gastrointestinal Neoplasms
Gastrointestinal tract
ABL
medicine.diagnostic_test
GiST
Cancer
Imatinib
Exons
Sequence Analysis, DNA
General Medicine
Middle Aged
medicine.disease
Molecular medicine
Proto-Oncogene Proteins c-kit
Pyrimidines
Oncology
Drug Resistance, Neoplasm
Benzamides
Mutation
Imatinib Mesylate
Cancer research
Female
Stromal Cells
medicine.drug
Subjects
Details
- ISSN :
- 17912431 and 1021335X
- Database :
- OpenAIRE
- Journal :
- Oncology Reports
- Accession number :
- edsair.doi.dedup.....7fbac693c3a8ac125dce3de14c8370d5
- Full Text :
- https://doi.org/10.3892/or.16.1.97