Evaluation of microRNA profile in cervical epithelium for predicting cervical cancer recurrence
- Authors: Maksimov A.Y.1, Timoshkova M.Y.1, Verenikina E.V.1, Lukbanova E.A.1, Kecheryukova M.M.2
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Affiliations:
- National Medical Research Centre for Oncology
- Rostov State Medical University
- Issue: Vol 48, No 5 (2020)
- Pages: 333-340
- Section: ARTICLES
- URL: https://almclinmed.ru/jour/article/view/1370
- DOI: https://doi.org/10.18786/2072-0505-2020-48-054
- ID: 1370
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Full Text
Abstract
Background: To predict the development and recurrence of cervical cancer (CC), we selected three oncoassociated miRNAs: miRNA-20a, -21, whose overexpression leads to the development of tumors, and -23b, which acts as an oncosuppressor. Aim: To evaluate the microRNA profile in the cervical epithelium for predicting CC recurrence in patients who underwent early treatment.
Materials and methods: In the study of the informativeness of expression included 145 patients with T1a1-T2a1N0M0 CC who were followed up for 2 years after treatment. Expression of microR-NA-20a, -21 and -23b was analyzed in tumor tissue samples.
Results: The risk of recurrence decreased from 1.0 to 0.92 after 1 year of the follow-up, and to 0.84 after 2 years. The initial expression of microRNA-20a and -21 in the cervical epithelium in patients with recurrent CC was 44% and 47% higher, respectively, than in patients without recurrence, while microRNA-23b expression was 46% lower. When initial levels of microRNA-20a and -21 expressions were 1.08 and 1.18, respectively, the risk of CC recurrence during the first two years after the surgery increased by 10.15 and 7.62 times, respectively. MicroRNA-20a expression in cervical epithelium equal to 1.08 was associated with 23% risk, and equal to 1.4 - with 79.7% risk. MicroRNA-21 expression equal to 1.18 was associated with 15% risk of CC recurrence; equal to 1.4 - with 55.5% risk; equal to 1.7 - 94.6%. Logistic regression showed that recurrence risks increased sharply when microRNA-23b expression declined.
Conclusion: We registered higher levels of mi-croRNA-20a and -21 expressions and lower mi-croRNA-23b expression in patients with recurrent CC, compared to favorable course of the disease. An analysis of the expression profiles of micro-RNA-20a, -21 and -23b after CC diagnosis allow prognosis of recurrence risks within 2 years after the tumor removal surgery.
Keywords
About the authors
A. Yu. Maksimov
National Medical Research Centre for Oncology
Author for correspondence.
Email: onko-sekretar@mail.ru
ORCID iD: 0000-0002-1397-837X
Aleksey Yu. Maksimov - MD, PhD, Professor, Deputy Director.
63 14-ya liniya, Rostov-on-Don, 344037; Tel.: +7 (863) 200 10 00; +7 (863) 300 02 00
РоссияM. Yu. Timoshkova
National Medical Research Centre for Oncology
Email: m-timoshkova@yandex.ru
ORCID iD: 0000-0003-1484-0580
Maria Yu. Timoshkova - MD, Oncologist, Junior Research Fellow, Experimental Laboratory Center.
63 14-ya liniya, Rostov-on-Don, 344037; Tel.: +7 (960) 489 80 80
РоссияE. V. Verenikina
National Medical Research Centre for Oncology
Email: ekat.veren@yandex.ru
ORCID iD: 0000-0002-1084-5176
Ekaterina V. Verenikina - MD, PhD, Head of Department of Oncogynecology.
63 14-ya liniya, Rostov-on-Don, 344037; Tel.: +7 (863) 300 02 00, ext. 380
РоссияE. A. Lukbanova
National Medical Research Centre for Oncology
Email: katya.samarskaja@yandex.ru
ORCID iD: 0000-0002-3036-6199
Ekaterina A. Lukbanova - Biologist, Research Fellow, Experimental Laboratory Center.
163 Azovskaya ul., Azov, Rostov Region, 346783, Tel.: +7 (928) 191 45 99
РоссияM. M. Kecheryukova
Rostov State Medical University
Email: adele09161@mail.ru
ORCID iD: 0000-0002-6131-8560
Madina M. Kecheryukova - Postgraduate Student.
29 Nakhichevanskiy pereulok, Rostov-on-Don, 344022; Tel.: +7 (928) 606 37 63
РоссияReferences
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