New undifferentiated pleomorphic sarcoma cell line UPS134 for in vitro and in vivo studies
- Authors: Shtompel P.A.1,2, Khazanova S.A.1,2, Trapeznikova E.S.1,3, Zinovieva V.Y.1, Lovenger A.A.1, Tararykova A.A.1, Bokhyan B.Y.1, Khromova N.V.1, Kopnin P.B.1, Fetisov T.I.1,2, Yakubovskaya M.G.1,2, Kirsanov K.I.1,2
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Affiliations:
- N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
- Patrice Lumumba Peoples’ Friendship University of Russia
- Russian Сenter of Neurology and Neuroscience
- Issue: Vol 25, No 1 (2026)
- Pages: 62-70
- Section: ORIGINAL REPORTS
- Published: 30.04.2026
- URL: https://bioterapevt.abvpress.ru/jour/article/view/1562
- DOI: https://doi.org/10.17650/1726-9784-2026-25-1-62-70
- ID: 1562
Cite item
Abstract
Background. Due to the limited number of cell lines, as well as the high heterogeneity of undifferentiated pleomorphic sarcomas (UPS), the creation of new stable cell lines is relevant.
Aim. Obtaining a stable cell line from a sample of UPS obtained during surgery to model carcinogenesis processes in vitro and in vivo.
Materials and methods. Cells were isolated from a tumor sample from a patient diagnosed with UPS. After passage 40 and stable growth, the proliferation rate, cell morphology, and growth ability in 3D culture conditions were assessed. To assess tumorigenicity, the cell suspension was injected into BALB / c nu / nu athymic mice. On the 15th day of the experiment, the tumor was removed, its volume was measured, and it was examined histologically. Using short tandem repeat (STR) analysis, the cells of the resulting line were examined for the presence of human cell markers and their uniqueness. The chemosensitivity of the cells was assessed using the resazurin test.
Results. Stable growth and formation of spheroids under 3D culturing conditions were demonstrated for the cell culture. All mice inoculated with the UPS134 cell suspension showed tumor growth, and by day 14 of the experiment its average size was 28,7 mm3. Histologically, the tumor is similar in morphology to UPS, except for a smaller amount of myxoid and less polymorphism. The cells of the obtained line were shown to contain all analyzed genetic markers of human cells, and also that the STR data of the obtained line did not coincide with the STR of other lines. For doxorubicin, gemcitabine and docetaxel, IC50 (inhibitory concentration) were determined to be 15, 6.5 and 10 % of the plasma peak concentration, respectively.
Conclusions. We obtained a new cell line UPS134, which can be further used to study the pathogenesis of UPS, as well as in preclinical studies of new antitumor agents in vitro and in vivo.
About the authors
Polina A. Shtompel
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Patrice Lumumba Peoples’ Friendship University of Russia
Author for correspondence.
Email: polina.shtooo@gmail.com
ORCID iD: 0009-0000-8673-597X
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 6 Miklukho-Maklaya St., Moscow 117198
Sofya A. Khazanova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Patrice Lumumba Peoples’ Friendship University of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-8350-0021
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 6 Miklukho-Maklaya St., Moscow 117198
Ekaterina S. Trapeznikova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Russian Сenter of Neurology and Neuroscience
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0001-6839-7436
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 80 Volokolamskoe Shosse, Moscow 125367
Victoria Yu. Zinovieva
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0003-2809-8487
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Anastasia A. Lovenger
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0009-0000-3317-9543
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Anastasia A. Tararykova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-5548-3295
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Beniamin Yu. Bokhyan
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-1396-3434
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Natalia V. Khromova
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0001-8348-6760
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Pavel B. Kopnin
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-2078-4274
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522
Timur I. Fetisov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Patrice Lumumba Peoples’ Friendship University of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-5082-9883
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 6 Miklukho-Maklaya St., Moscow 117198
Marianna G. Yakubovskaya
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Patrice Lumumba Peoples’ Friendship University of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-9710-8178
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 6 Miklukho-Maklaya St., Moscow 117198
Kirill I. Kirsanov
N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Patrice Lumumba Peoples’ Friendship University of Russia
Email: polina.shtooo@gmail.com
ORCID iD: 0000-0002-8599-6833
Russian Federation, 24 Kashirskoe Shosse, Moscow 115522; 6 Miklukho-Maklaya St., Moscow 117198
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