1. FMS mutations in patients following cytotoxic therapy for lymphoma
- Author
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Richard Clarke, Ridge Sa, Hugh McGlynn, Andrew H. Baker, Rose Ann Padua, Phillip Cachia, Allan Jacobs, and J. A. Whittaker
- Subjects
Adult ,Male ,Cancer Research ,Molecular Sequence Data ,Mutant ,Population ,Antineoplastic Agents ,medicine.disease_cause ,Proto-Oncogene Mas ,hemic and lymphatic diseases ,Proto-Oncogenes ,Biopsy ,medicine ,Humans ,education ,Gene ,Polymorphism, Single-Stranded Conformational ,Aged ,DNA Primers ,Mutation ,education.field_of_study ,Base Sequence ,medicine.diagnostic_test ,Cytotoxins ,business.industry ,Lymphoma, Non-Hodgkin ,Point mutation ,Single-strand conformation polymorphism ,Genes, fms ,Hematology ,Middle Aged ,medicine.disease ,Hodgkin Disease ,Lymphoma ,Genes, ras ,Oncology ,Immunology ,Cancer research ,Female ,business - Abstract
Point mutations at codons 301 and 969 of the FMS proto-oncogene have been reported in both myelodysplasia (MDS) and acute myeloid leukaemia (AML). We report here the incidence of such mutations in patients at risk of developing secondary MDS and AML. Peripheral blood DNA from 70 patients in remission from lymphoma was screened for mutations by oligonucleotide (ONH) using mutant specific probes. Codon 969 mutations were detected in 11 of the 70 (15.7%) cases. No codon 301 mutations were detected. Five of these mutations were confirmed using an independent technique (single nucleotide primer extension analysis, SNPE) and a further mutation was detected in a single patient using single-stranded conformational polymorphism analysis (SSCP). No codon 969 mutations were detected in 62 lymphoma biopsy specimens from these patients or from three patients with detectable FMS mutations where pre-therapy marrow was investigated by ONH. No mutations at either codons 301 or 969 were detected by ONH in 61 normal controls. Somatic mutations at codon 969 of the FMS gene occur commonly following cytotoxic therapy for lymphoma and their detection indicates the presence of a clonally expanded population of abnormal cells.
- Published
- 1995