Expression and Clinicopathological Significances of lncRNAs: Could ARA and ZEB2NAT be the Potential Breast Cancer-Related Biomarkers?


Journal

Archives of medical research
ISSN: 1873-5487
Titre abrégé: Arch Med Res
Pays: United States
ID NLM: 9312706

Informations de publication

Date de publication:
11 2020
Historique:
received: 29 12 2019
revised: 10 04 2020
accepted: 01 09 2020
pubmed: 15 9 2020
medline: 20 2 2021
entrez: 14 9 2020
Statut: ppublish

Résumé

Pieces of evidence have shown that a significant proportion of cancer-prone factors are not attributed to alterations in protein-coding sequences. Adriamycin resistance-related (ARA) and natural antisense of ZEB2 (ZEB2NAT) long non-coding RNAs (lncRNAs) have been indicated with oncogenic properties by regulating various signaling pathways and epithelial-to-mesenchymal transition (EMT), which may have diagnostic and prognostic potential as a novel group of biomarkers. The current study aimed to evaluate the expression status of ARA and ZEB2NAT lncRNAs and their clinicopathological significance in a population with breast cancer (BC). Total RNA was extracted from 60 tumor samples and their normal adjacent tissues (NATs). The lncRNA expressions were measured using quantitative reverse transcription PCR (RT-qPCR) and statistical analyses were performed by SPSS version 25. Our data showed a significant upregulation of ARA and ZEB2NAT lncRNAs in tumor tissues compared to NATs (p <0.001; p = 0.021, respectively). ARA and ZEB2NAT expression were observed to be significantly associated with tumor grade, nuclear grade, tumor stages, and lymph node metastasis (p <0.05). Additionally, ARA expression was significantly correlated with breastfeeding status (p = 0.027). our data revealed that ARA and ZEB2NAT lncRNAs were overexpressed in BC. Furthermore, the selected lncRNAs were found to might be the potential biomarkers for BC diagnosis and prognosis. However, the findings of the current research are required to be replicated in other studies with larger sample sizes.

Identifiants

pubmed: 32921528
pii: S0188-4409(19)31324-4
doi: 10.1016/j.arcmed.2020.09.002
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
RNA, Long Noncoding 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

851-859

Informations de copyright

Copyright © 2020 IMSS. Published by Elsevier Inc. All rights reserved.

Auteurs

Sara Hesami (S)

Medical Genetics Ward, Imam khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.

Maliheh Sayar (M)

Nursing And Midwifery School, Mashhad University of Medical Sciences, Mashhad, Iran.

Fahimeh Sayyar (F)

Nursing And Midwifery School, Birjand University Of Medical Science, Birjand, Iran.

Yeganeh Eshaghkhani (Y)

Department of Medical Genetics, School of Medicine, Tehran University of Medical Science, Tehran, Iran.

Maryam Pirhoushiaran (M)

Department of Medical Genetics, School of Medicine, Tehran University of Medical Science, Tehran, Iran.

Mohammad Bagher Khadem Erfan (MB)

Department of Parasitology and Mycology, Faculty of Medicine, Kurdistan University of Medical Science, Sanandaj, Iran.

Rasoul Abdollahzadeh (R)

Department of Medical Genetics, School of Medicine, Tehran University of Medical Science, Tehran, Iran.

Asaad Azarnezhad (A)

Cellular and Molecular Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran; Liver and Digestive Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran. Electronic address: Azarnezhad@gmail.com.

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Classifications MeSH