Clinical significance of blood-based miRNAs as diagnostic and prognostic nucleic acid markers in breast cancer: Comparative to conventional tumor markers.


Journal

Journal of cellular biochemistry
ISSN: 1097-4644
Titre abrégé: J Cell Biochem
Pays: United States
ID NLM: 8205768

Informations de publication

Date de publication:
08 2019
Historique:
received: 05 11 2018
revised: 17 12 2018
accepted: 07 01 2019
pubmed: 3 3 2019
medline: 28 8 2020
entrez: 3 3 2019
Statut: ppublish

Résumé

microRNAs (miRNAs) are implicated in carcinogenesis and their expression in biological fluids offer great potential as nucleic acid markers for cancer detection and progression. Authors investigated the expression level of miRNAs (miRNA-21, miRNA-126, and miRNA-155) to evaluate their role as diagnostic and prognostic markers for breast cancer compared with other commonly used protein-based markers (CEA and CA15-3). Serum samples from patients with breast cancer (n = 96), patients with benign breast lesion (n = 47), and healthy individuals (n = 39) were enrolled for detection of miRNA expression levels and protein-based tumor markers using fluorescent real-time quantitative polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Correlation among investigated markers with clinicopathological factors and clinical outcomes were determined. Expression of miRNA-21 and miRNA-155 revealed significant increases in patients with breast cancer compared with both benign and control groups, the same result was reported for tumor markers; on the other hand, miRNA-126 was significantly decreased in breast cancer group as compared with the other two groups. miRNA frequencies were significantly related to clinical staging and histological grading as compared with tumor markers. Patients with breast cancer with increased miRNA-21 and miRNA-155 and decreased miRNA-126 expressions had significantly worse disease-free survival, while only miRNA-21 and miRNA-126 showed poor OS (P< 0.005). In conclusion, investigated miRNAs were superior over tumor markers for the early stage of breast cancer especially those with high-risk factor and their assessment in blood facilitates their role as a potential prognostic molecular marker.

Identifiants

pubmed: 30825229
doi: 10.1002/jcb.28496
doi:

Substances chimiques

Biomarkers, Tumor 0
MIRN126 microRNA, human 0
MIRN155 microRNA, human 0
MIRN21 microRNA, human 0
MicroRNAs 0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

12321-12330

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Menha Swellam (M)

Biochemistry Department Genetic Engineering and Biotechnology Research Division, National Research Centre, Giza, Egypt.
High Throughput Molecular and Genetic Laboratory, Center for Excellence for Advanced Sciences, National Research Centre, Giza, Egypt.

Amal Ramadan (A)

Biochemistry Department Genetic Engineering and Biotechnology Research Division, National Research Centre, Giza, Egypt.
High Throughput Molecular and Genetic Laboratory, Center for Excellence for Advanced Sciences, National Research Centre, Giza, Egypt.

Enas A El-Hussieny (EA)

Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.

Noha M Bakr (NM)

Biochemistry Department Genetic Engineering and Biotechnology Research Division, National Research Centre, Giza, Egypt.
High Throughput Molecular and Genetic Laboratory, Center for Excellence for Advanced Sciences, National Research Centre, Giza, Egypt.

Naglaa M Hassan (NM)

Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.

Mohamed Emam Sobeih (ME)

Medical Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt.

Lobna R EzzElArab (LR)

Clinical Oncology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

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Classifications MeSH