Alternative Splicing and Leukemia Initiating Cells
- Conditions
- Acute Myeloid Leukemia
- Interventions
- Other: Assessment of splicing variants
- Registration Number
- NCT03156933
- Lead Sponsor
- Hospices Civils de Lyon
- Brief Summary
Aberrant RNA splicing and mutations in spliceosome complex in acute myeloid leukaemia (AML) are frequent. It have been shown that some splicing variants had a prognostic value in AML.
AML are characterized by their propensity to relapse because of the persistence of leukaemia initiating cells (LICs).
The aim of this study is to determine the splice variants on AML initiator cells and define a splicing pattern.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 500
- Age ≥ 18 years-old
- Patients treated at the south lyon hospital center
- Patients with a diagnosis of acute myeloid leukemia confirmed in cytology and whose involvement of the 11q23 locus was confirmed by in situ hybridization
- Patients for whom a sample is available in the cytogenetic laboratory of the south lyon hospital center
None
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Splicing variants Assessment of splicing variants Sample of acute myeloid leukaemia primary cells
- Primary Outcome Measures
Name Time Method Polymerase chain reaction 1 month Transcriptome analysis to determine the splicing variants on acute myeloid leukaemia initiator cells.
The analysis will focus on the gene encoding ABCA3 transporter and genes known to be mutated in patients with acute myeloid leukemia (FLT3, NPM1, c-Kit, N et K-RAS).
The duration of selection of samples is estimated to be one month.Ribonucleic acid sequencing 1 month Transcriptome analysis to determine the splicing variants on acute myeloid leukaemia initiator cells.
The analysis will focus on the gene encoding ABCA3 transporter and genes known to be mutated in patients with acute myeloid leukemia (FLT3, NPM1, c-Kit, N et K-RAS).
The duration of selection of samples is estimated to be one month.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Service d'hématologie du Centre Hospitalier Lyon Sud
🇫🇷Pierre-Bénite, France