Biobanking prostate tissue
- Authors: Asfandiyarova I.V.1, Vlasova A.O.1, Velikomolova Y.B.1, Shchekin V.S.1, Urmantsev M.F.1, Pavlov V.N.1
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Affiliations:
- Bashkir State Medical University, Ministry of Health of Russia
- Issue: Vol 21, No 2 (2025)
- Pages: 82-88
- Section: DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. PROSTATE CANCER
- Published: 06.08.2025
- URL: https://oncourology.abvpress.ru/oncur/article/view/1924
- DOI: https://doi.org/10.17650/1726-9776-2025-21-2-82-88
- ID: 1924
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Full Text
Abstract
Background. Prostate cancer is the most common malignant disease in men. Obtaining high quality and diagnostically accurate tissue samples is paramount to the success of prostate cancer research. Collecting unfixed tissues from radical prostatectomy specimens for research purposes is challenging. Prostate cancer often cannot be detected on gross examination, and this tumor is known to be multifocal and heterogeneous making it of interest for interdisciplinary research.
Aim. To develop a protocol that will improve the accuracy and quantity of biobanked primary prostate cancer tissue.
Materials and methods. The removed unfixed prostate gland was dissected with a blade into two halves along the ureter, the tumor lesion was identified macroscopically, two sections were made: the first was separated into fragments and transferred into cryotubes and transport media for biobanking storage; the second was filled with gel, and frozen sectioning and histological verification of the tumor were performed.
Results. Tumor was detected in frozen sections in 78.95 % (30/38) of cases. The mean time from organ removal from the abdominal cavity to macroscopic evaluation was 8–10 minutes, and the total time for histological verification was 30 minutes. The quality control performed on the biobanked material confirms that the developed protocol guarantees that both tumors and normal tissues are represented for further studies.
Conclusion. This paper outlines a method for biobanking fresh prostate tissue removed during radical prostatectomy. The advantage of the method is the use of tissue samples both for diagnosis and for further study at the cellular and molecular levels.
Keywords
About the authors
I. V. Asfandiyarova
Bashkir State Medical University, Ministry of Health of Russia
Email: i.asfan@mail.ru
ORCID iD: 0000-0003-2760-7454
SPIN-code: 8756-5188
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationA. O. Vlasova
Bashkir State Medical University, Ministry of Health of Russia
Author for correspondence.
Email: angvlon@mail.ru
ORCID iD: 0009-0002-1818-5077
SPIN-code: 7999-8086
Angelina Olegovna Vlasova
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationYu. B. Velikomolova
Bashkir State Medical University, Ministry of Health of Russia
Email: welikomolowa@yandex.ru
ORCID iD: 0009-0002-9786-9126
SPIN-code: 3216-4006
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationV. S. Shchekin
Bashkir State Medical University, Ministry of Health of Russia
Email: vlas-s@mail.ru
ORCID iD: 0000-0003-2202-7071
SPIN-code: 7796-0630
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationM. F. Urmantsev
Bashkir State Medical University, Ministry of Health of Russia
Email: urmantsev85@mail.ru
ORCID iD: 0000-0002-4657-6625
SPIN-code: 3506-7753
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationV. N. Pavlov
Bashkir State Medical University, Ministry of Health of Russia
Email: rectorat@bashgmu.ru
ORCID iD: 0000-0003-2125-4897
SPIN-code: 2799-6268
3 Lenina St., Ufa 450008, Republic of Bashkortostan
Russian FederationReferences
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