Expression of HOTAIR and PTGS2 as potential biomarkers in chronic myeloid leukemia patients in Brazil
Chronic myeloid leukemia (CML) is a clonal myeloproliferative neoplasm in which all the patients has the translocation ( ) that generates de BCR::ABL1 tyrosine kinase. Despite this disease possessing a good biomarker ( transcripts level) for diagnosis and prognosis, many studies has been performed t...
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Published in: | Frontiers in oncology Vol. 14; p. 1443346 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
Frontiers Media S.A
10-10-2024
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Subjects: | |
Online Access: | Get full text |
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Summary: | Chronic myeloid leukemia (CML) is a clonal myeloproliferative neoplasm in which all the patients has the translocation (
) that generates de BCR::ABL1 tyrosine kinase. Despite this disease possessing a good biomarker (
transcripts level) for diagnosis and prognosis, many studies has been performed to investigate other molecules, such as the long noncoding RNAs (lncRNAs) and mRNAs, as potential biomarkers with the aim of predicting a change in
levels and as an associated biomarker. A RNAseq was performed comparing 6 CML patients with high
expression with 6 healthy control individuals, comprising the investigation cohort to investigate these molecules. To validate the results obtained by RNAseq, samples of 87 CML patients and 42 healthy controls were used in the validation cohort by RT-qPCR assays. The results showed lower expression of
and
in CML patients. The
expression is inversely associated with
expression in imatinib-treated CML patients, and to
showing that CML patients with high
expression showed reduced
expression. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Rui Liu, Xi’an Jiaotong University, China Reviewed by: Apurva Patel, Gujarat Cancer & Research Institute, India Edited by: Jixin Dong, University of Nebraska Medical Center, United States Yanlong Shi, Nanjing Medical University, China |
ISSN: | 2234-943X 2234-943X |
DOI: | 10.3389/fonc.2024.1443346 |