Diagnostic and prognostic value of long non-coding RNA PROX1‑AS1 and miR-647 expression in gastric cancer
- Authors: Vetchinkina E.A.1, Kalinkin A.I.2, Kuznetsova E.B.1,2, Kiseleva A.E.1, Alekseeva E.A.1,2, Nemtsova M.V.1,2, Bure I.V.1
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Affiliations:
- I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
- N.P. Bochkov Medical and Genetic Research Center
- Issue: Vol 9, No 4 (2022)
- Pages: 50‑60
- Section: RESEARCH ARTICLES
- Published: 17.12.2022
- URL: https://umo.abvpress.ru/jour/article/view/476
- DOI: https://doi.org/10.17650/2313-805X-2022-9-4-50-60
- ID: 476
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Abstract
Introduction. Gastric cancer remains one of the most common cancers and has a high mortality rate worldwide. Epigenetic alternations of non-coding RNAs (ncRNAs), including microRNAs and long ncRNAs can contribute to its pathogenesis and progression, and could be potent diagnostic and prognostic biomarkers.
Aim. Estimation of PROX1‑AS1 and miR-647 expression in gastric cancer and investigation of its clinical significance. Materials and methods. Tumor and adjacent normal tissues (n = 62), and sectional normal tissue samples (n = 5) were included in the study. The expression of the ncRNAs was quantified by reverse transcription-polymerase chain reaction assay.
Results. We have reviled the significant difference in the PROX1‑AS1 expression in tumor (p = 0.002) and non-tumor tissues (p <0.001) obtained from gastric cancer patients in comparison with sectional gastric tissues without pathology. Pearson correlation analysis confirmed a negative correlation between PROX1‑AS1 and miR-647 in gastric cancer both in tumor (р <0,001) and adjacent normal tissues (р <0.001). Besides, expression of PROX1‑AS1 and miR-647 was associated with the size and extent of the primary tumor.
Conclusion. The obtained results allow to suggest a potential prognostic value of PROX1‑AS1 and miR-647 in gastric cancer.
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About the authors
E. A. Vetchinkina
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Author for correspondence.
Email: katevetchinkina@ya.ru
ORCID iD: 0000-0001-8069-5540
Ekaterina Alexandrovna Vetchinkina
Bld. 2 8 Trubetskaya St., Moscow 119991
Russian FederationA. I. Kalinkin
N.P. Bochkov Medical and Genetic Research Center
Email: fake@neicon.ru
ORCID iD: 0000-0001-9215-4581
1 Moskvorechye St., Moscow 115522
Russian FederationE. B. Kuznetsova
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia; N.P. Bochkov Medical and Genetic Research Center
Email: fake@neicon.ru
ORCID iD: 0000-0001-5825-0430
Bld. 2 8 Trubetskaya St., Moscow 119991
1 Moskvorechye St., Moscow 115522
Russian FederationA. E. Kiseleva
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0002-6930-1261
Bld. 2 8 Trubetskaya St., Moscow 119991
Russian FederationE. A. Alekseeva
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia; N.P. Bochkov Medical and Genetic Research Center
Email: fake@neicon.ru
ORCID iD: 0000-0002-7035-1362
Bld. 2 8 Trubetskaya St., Moscow 119991
1 Moskvorechye St., Moscow 115522
Russian FederationM. V. Nemtsova
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia; N.P. Bochkov Medical and Genetic Research Center
Email: fake@neicon.ru
ORCID iD: 0000-0002-2835-5992
Bld. 2 8 Trubetskaya St., Moscow 119991
1 Moskvorechye St., Moscow 115522
Russian FederationI. V. Bure
I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia
Email: fake@neicon.ru
ORCID iD: 0000-0003-2043-5848
Bld. 2 8 Trubetskaya St., Moscow 119991
Russian FederationReferences
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