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Series GSE229046 Query DataSets for GSE229046
Status Public on May 22, 2024
Title MIR4435-2HG as a novel predictive biomarker of chemotherapy response and death in pediatric B-cell ALL [RNA-seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary B-cell acute lymphoid leukemias (B-ALL) are the most common neoplastic diseases in children. Survival rates in Hispanics are lower than in non-Hispanic children. It is, therefore, necessary to find predictive and prognostic biomarkers of relapse and death in this population. Our aim was to identify biomarkers of treatment response, which may also predict relapse and death, through identifying differentially expressed and methylated genes between patients who responded or did not respond to induction treatment. DNA and RNA samples were extracted from 28 bone marrow samples from Hispanic children newly diagnosed with B-ALL. mRNA was sequenced using the NextSeq2000 Illumina platform. Bisulfite-treated DNA was annealed to Illumina Infinium EPIC Methylation chips. Gene expression and differential methylation were compared between responders and non-responders at day 15 and at the end of induction chemotherapy. DAPK1, CNKSR3, MIR4435-HG2, CTHRC1, NPDC1, SLC45A3, ITGA6, and ASCL2 were overexpressed and hypomethylated in non-responders. The overexpression of MIR4435-2HG, DAPK1, ASCL2, SCL45A3, CNKSR3, and NPDC1 can predict non-response at day 15 and refractoriness. Additionally, higher expression of MIR4435-2HG increases the probability of non-response, death, and the risk of death. DAPK1, CNKSR3, and MIR4435-2HG are also overexpressed in relapse samples. Finally, MIR4435-2HG overexpression, together with positive minimal residual disease, is associated with poorer survival, and together with high expression of DAPK1 and ASCL2, it could improve the risk classification of patients with normal karyotype. In conclusion, MIR4435-2HG is a potential predictive and prognostic biomarker in children with B-ALL, and its detection at diagnosis could improve survival rates in our patients
 
Overall design 26 fresh bone marrow samples.
 
Contributor(s) Torres-Llanos YX, Zabaleta J, Cruz-Rodriguez N, Quijano SM, Guzman PC, de los Reyes I, Poveda N, Infante A, Lopez L, Combita AL
Citation(s) 38745909
Submission date Apr 05, 2023
Last update date May 22, 2024
Contact name Jovanny Zabaleta
E-mail(s) jzabal@lsuhsc.edu
Phone 504-210 2979
Organization name Louisiana State University Health Sciences Center
Department Cancer Center/Interdiscipliary Oncology
Lab LCRC 909
Street address 1700 Tulane Ave.
City New Orleans
State/province LA
ZIP/Postal code 70112
Country USA
 
Platforms (1)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (26)
GSM7148304 KDA013
GSM7148305 DSR017
GSM7148306 JSR021
This SubSeries is part of SuperSeries:
GSE229056 MIR4435-2HG as a novel predictive biomarker of chemotherapy response and death in pediatric B-cell ALL
Relations
BioProject PRJNA952635

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SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE229046_XimenaTorresLlanos_AllSamples_Raw_counts.txt.gz 1.3 Mb (ftp)(http) TXT
GSE229046_XimenaTorres_Llanos_AllSamples_Normalized_counts.txt.gz 1.8 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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