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Integration of miRNA expression analysis of purified leukocytes and whole blood reveals blood-borne candidate biomarkers for lung cancer.
- Source :
-
Epigenetics [Epigenetics] 2024 Dec; Vol. 19 (1), pp. 2393948. Date of Electronic Publication: 2024 Aug 20. - Publication Year :
- 2024
-
Abstract
- Changes in leukocyte populations may confound the disease-associated miRNA signals in the blood of cancer patients. We aimed to develop a method to detect differentially expressed miRNAs from lung cancer whole blood samples that are not influenced by variations in leukocyte proportions. The Ref-miREO method identifies differential miRNAs unaffected by changes in leukocyte populations by comparing the within-sample relative expression orderings (REOs) of miRNAs from healthy leukocyte subtypes and those from lung cancer blood samples. Over 77% of the differential miRNAs observed between lung cancer and healthy blood samples overlapped with those between myeloid-derived and lymphoid-derived leukocytes, suggesting the potential impact of changes in leukocyte populations on miRNA profile. Ref-miREO identified 16 differential miRNAs that target 19 lung adenocarcinoma-related genes previously linked to leukocytes. These miRNAs showed enrichment in cancer-related pathways and demonstrated high potential as diagnostic biomarkers, with the LASSO regression models effectively distinguishing between healthy and lung cancer blood or serum samples (all AUC > 0.85). Additionally, 12 of these miRNAs exhibited significant prognostic correlations. The Ref-miREO method offers valuable candidates for circulating biomarker detection in cancer that are not affected by changes in leukocyte populations.
- Subjects :
- Humans
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Male
Female
Adenocarcinoma of Lung genetics
Adenocarcinoma of Lung blood
Lung Neoplasms genetics
Lung Neoplasms blood
Biomarkers, Tumor blood
Biomarkers, Tumor genetics
Leukocytes metabolism
MicroRNAs blood
MicroRNAs genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1559-2308
- Volume :
- 19
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Epigenetics
- Publication Type :
- Academic Journal
- Accession number :
- 39164937
- Full Text :
- https://doi.org/10.1080/15592294.2024.2393948