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NOTCH1 mutations in +12 chronic lymphocytic leukemia (CLL) confer an unfavorable prognosis, induce a distinctive transcriptional profiling and refine the intermediate prognosis of +12 CLL
- Publication Year :
- 2012
- Publisher :
- Ferrata Storti Foundation, 2012.
-
Abstract
- Trisomy 12, the third most frequent chromosomal aberration in chronic lymphocytic leukemia (CLL), confers an intermediate prognosis. In our cohort of 104 untreated patients carrying +12, NOTCH1 mutations occurred in 24% of cases and were associated to unmutated IGHV genes (P=0.003) and +12 as a sole cytogenetic abnormality (P=0.008). NOTCH1 mutations in +12 CLL associated with an approximately 2.4 fold increase in the risk of death, a significant shortening of survival (P
- Subjects :
- Male
Transcription, Genetic
Chronic lymphocytic leukemia
Trisomy
Biology
Independent predictor
Chromosomes
trisomy 12
Mutation Rate
immune system diseases
Cytogenetic Abnormality
hemic and lymphatic diseases
medicine
Pair 12
Humans
Receptor, Notch1
Gene
neoplasms
Aged
Chromosomes, Human, Pair 12
Gene Expression Profiling
notch1 mutations
Hematology
Middle Aged
Cell cycle
Chronic Lymphocytic Leukemia
NOTCH1
prognosis
medicine.disease
Survival Analysis
Leukemia, Lymphocytic, Chronic, B-Cell
Settore MED/15 - MALATTIE DEL SANGUE
Immunology
Mutation
Cancer research
chronic lymphocytic leukemia
gene expression profile
Female
Risk of death
Original Articles and Brief Reports
IGHV@
Human
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....2870a1fc42b5415dd39579d2fd281c26