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Transplantation of mitochondria from human malignant tumor cells as a method of tumor growth formation in the lungs of laboratory animals

https://doi.org/10.17709/2410-1893-2023-10-4-5

EDN: NDLLNM

Abstract

Purpose of the study. Obtaining lung cancer tumors in Balb/c Nude mice by transplantation of mitochondria isolated from human malignant tumors.

Materials and methods. Human lung cancer mitochondria were isolated using differential centrifugation on a high-speed refrigerated centrifuge. Mitochondrial samples were diluted with 0.9 % NaCl solution to a protein concentration of 3 mg per animal. Freshly isolated lung cancer mitochondria were once transplanted into the tail vein of male Balb/c Nude mice (n = 6) at the rate of 3 mg of protein per 1 animal in 0.4 ml of saline. Male mice of Balb/c Nude line (n = 4), which were injected with 0.4 ml of physiological solution into the tail vein once a day, served as a control group. All animals were killed by guillotine decapitation 4 months after intravenous transplantation of mitochondria isolated from lung cancer.

Results. After the introduction of mitochondria into the tail vein of mice, no changes were found in the animals’ behavior, coloration of coverings. No respiratory problems, and no allergic reactions to the introduction of foreign protein were detected. Respiratory problems in mice with mitochondrial transplantation occurred between days 113 and 123, when a drop in body weight ≥ 25 % was observed. A uniform formation of tumor nodes together with an active filling of the lung space with blood was clearly visible on lung preparations of a Balb/c Nude male mouse after intravenous transplantation of mitochondria from the lung of a patient with non-keratinizing squamous cell carcinoma. Similar characteristics of tumor growth in the lung parenchyma of the patient and Balb/c Nude mice as direct recipients of tumor mitochondria involved solid structures consisting of fields, cells and strands of tightly fitting atypical polymorphic cells of the squamous epithelium with poorly developed cytoplasm. In addition, signs of adenocarcinoma included glandular and papillary-like structures and cell complexes with large nucleoli. Squamous epithelial cells were characterized by severe atypia and polymorphism. The shape of the nuclei was irregular in most cells, with large sizes, the color was heterogeneous, and the nucleoli were enlarged. Multinucleated cells, as well as pathological mitoses with clearly marked division figures, which testified to their proliferative activity, were encountered with a rather high frequency.

Conclusions. Application of intravenous transplantation of mitochondria isolated from malignant human lung tumor in male mice of Balb/c Nude line causes growth and development of malignant foci in male Balb/c Nude mice. This is previously unknown fact in experimental oncology, allowing the study of new properties of mitochondria of human cancer cells.

About the Authors

O. I. Kit
National Medical Research Centre for Oncology of the Ministry of Health of Russia

Rostov-on-Don, Russian Federation

 

Oleg I. Kit – Academician of RAS, Dr. Sci. (Medicine), Professor, General Director of National Medical Research Centre for Oncology of the Ministry of Health of Russia, Rostov-on-Don, Russian Federation

ORCID: https://orcid.org/0000-0003-3061-6108, SPIN: 1728-0329, AuthorID: 343182, Scopus Author ID: 55994103100, Researcher ID: U-2241-2017


Competing Interests:

Author state that there are no conflicts of interest to disclose.



E. M. Frantsiyants
National Medical Research Centre for Oncology of the Ministry of Health of Russia

Rostov-on-Don, Russian Federation

 

Elena M. Frantsiyants – Dr. Sci. (Biology), Professor, Deputy General Director for Science of National Medical Research Centre for Oncology of the Ministry of Health of Russia, Rostov-on-Don, Russian Federation

ORCID: https://orcid.org/0000-0003-3618-6890, SPIN: 9427-9928, Author ID: 462868, Scopus Author ID: 55890047700, Researcher ID: Y-1491-2018


Competing Interests:

Author state that there are no conflicts of interest to disclose.



A. I. Shikhlyarova
National Medical Research Centre for Oncology of the Ministry of Health of Russia

Rostov-on-Don, Russian Federation

 

Alla I. Shikhlyarova – Dr. Sci. (Biology), Professor, Senior Researcher at Laboratory of Malignant Tumor Pathogenesis Study, National Medical Research Centre for Oncology of the Ministry of Health of Russia, Rostov-on-Don, Russian Federation

ORCID: https://orcid.org/0000-0003-2943-7655, SPIN: 6271-0717, Author ID: 482103, Scopus Author ID: 57312836900, Researcher ID: Y-6275-2018


Competing Interests:

Author state that there are no conflicts of interest to disclose.



I. V. Neskubina
National Medical Research Centre for Oncology of the Ministry of Health of Russia

Rostov-on-Don, Russian Federation

 

Irina V. Neskubina – Cand. Sci. (Biology), Senior Researcher at Laboratory of Malignant Tumor Pathogenesis Study, National Medical Research Centre for Oncology of the Ministry of Health of Russia, Rostov-on-Don, Russian Federation

ORCID: https://orcid.org/0000-0002-7395-3086, SPIN: 3581-8531, AuthorID: 794688, Scopus Author ID: 6507509066, ResearcherID: AAG-8731-2019


Competing Interests:

Author state that there are no conflicts of interest to disclose.



References

1. Liu W, Cui Y, Zheng X, Yu K, Sun G. Application status and future prospects of the PDX model in lung cancer. Front Oncol. 2023 Mar 24;13:1098581. https://doi.org/10.3389/fonc.2023.1098581

2. Kutilin DS, Airapetova TG, Anistratov PA, Pyltsin SP, Leiman IA, Karnaukhov NS, Kit OI. Copy number variation in tumor cells and extracellular DNA in patients with lung adenocarcinoma. Bulletin of Experimental Biology and Medicine. 2019;167(6):771–778.

3. Firestone B. The challenge of selecting the ‘right’ in vivo oncology pharmacology model. Curr Opin Pharmacol. 2010 Aug;10(4):391– 396. https://doi.org/10.1016/j.coph.2010.06.012

4. Ibarrola-Villava M, Cervantes A, Bardelli A. Preclinical models for precision oncology. Biochim Biophys Acta Rev Cancer. 2018 Dec;1870(2):239-246. https://doi.org/10.1016/j.bbcan.2018.06.004 Epub 2018 Jun 28. Erratum in: Biochim Biophys Acta Rev Cancer. 2019 Dec;1872(2):188292

5. Jing X, Yang F, Shao C, Wei K, Xie M, Shen H, Shu Y. Role of hypoxia in cancer therapy by regulating the tumor microenvironment. Mol Cancer. 2019 Nov 11;18(1):157. https://doi.org/10.1186/s12943-019-1089-9

6. Dong L, Gopalan V, Holland O, Neuzil J. Mitocans Revisited: Mitochondrial Targeting as Efficient Anti-Cancer Therapy. Int J Mol Sci. 2020 Oct 26;21(21):7941. https://doi.org/10.3390/ijms21217941

7. Damaghi M, West J, Robertson-Tessi M, Xu L, Ferrall-Fairbanks MC, Stewart PA, et al. The harsh microenvironment in early breast cancer selects for a Warburg phenotype. Proc Natl Acad Sci U S A. 2021 Jan 19;118(3):e2011342118. https://doi.org/10.1073/pnas.2011342118

8. Humpton TJ, Alagesan B, DeNicola GM, Lu D, Yordanov GN, Leonhardt CS, et al. Oncogenic KRAS Induces NIX-Mediated Mitophagy to Promote Pancreatic Cancer. Cancer Discov. 2019 Sep;9(9):1268–1287. https://doi.org/10.1158/2159-8290.cd-18-1409

9. Cogliati S, Frezza C, Soriano ME, Varanita T, Quintana-Cabrera R, Corrado M, et al. Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency. Cell. 2013 Sep 26;155(1):160–171. https://doi.org/10.1016/j.cell.2013.08.032

10. Singh B, Modica-Napolitano JS, Singh KK. Defining the momiome: Promiscuous information transfer by mobile mitochondria and the mitochondrial genome. Semin Cancer Biol. 2017 Dec;47:1–17. https://doi.org/10.1016/j.semcancer.2017.05.004

11. Shanmughapriya S, Langford D, Natarajaseenivasan K. Inter and Intracellular mitochondrial trafficking in health and disease. Ageing Res Rev. 2020 Sep;62:101128. https://doi.org/10.1016/j.arr.2020.101128

12. Walters HE, Cox LS. Intercellular Transfer of Mitochondria between Senescent Cells through Cytoskeleton-Supported Intercellular Bridges Requires mTOR and CDC42 Signalling. Oxid Med Cell Longev. 2021 Jul 31;2021:6697861. https://doi.org/10.1155/2021/6697861

13. Ali Pour P, Hosseinian S, Kheradvar A. Mitochondrial transplantation in cardiomyocytes: foundation, methods, and outcomes. Am J Physiol Cell Physiol. 2021 Sep 1;321(3):C489–C503. https://doi.org/10.1152/ajpcell.00152.2021

14. Park A, Oh M, Lee SJ, Oh KJ, Lee EW, Lee SC, Bae KH, Han BS, Kim WK. Mitochondrial Transplantation as a Novel Therapeutic Strategy for Mitochondrial Diseases. Int J Mol Sci. 2021 Apr 30;22(9):4793. https://doi.org/10.3390/ijms22094793

15. Russell OM, Gorman GS, Lightowlers RN, Turnbull DM. Mitochondrial Diseases: Hope for the Future. Cell. 2020 Apr 2;181(1):168– 188. https://doi.org/10.1016/j.cell.2020.02.051

16. Sidarala V, Pearson GL, Parekh VS, Thompson B, Christen L, Gingerich MA, Zhu J, Stromer T, Ren J, Reck EC, Chai B, Corbett JA, Mandrup-Poulsen T, Satin LS, Soleimanpour SA. Mitophagy protects β cells from inflammatory damage in diabetes. JCI Insight. 2020 Dec 17;5(24):e141138. https://doi.org/10.1172/jci.insight.141138

17. Liu Z, Sun Y, Qi Z, Cao L, Ding S. Mitochondrial transfer/transplantation: an emerging therapeutic approach for multiple diseases. Cell Biosci. 2022 May 19;12(1):66. https://doi.org/10.1186/s13578-022-00805-7

18. Egorova MV, Afanasyev SA. Isolation of mitochondria from cells and tissues of animals and human: modern methodical approaches. Siberian Medical Journal. 2011;26(1–1):22–28. (In Russ.).

19. Gureev AP, Kokina AV, Syromyatnikov MYu, Popov VN. Optimization of methods for the mitochondria isolation from different mice tissues. Proceedings of Voronezh State University. Series: Chemistry. Biology. Pharmacy. 2015;4:61–65. (In Russ.).


Review

For citations:


Kit O.I., Frantsiyants E.M., Shikhlyarova A.I., Neskubina I.V. Transplantation of mitochondria from human malignant tumor cells as a method of tumor growth formation in the lungs of laboratory animals. Research and Practical Medicine Journal. 2023;10(4):59-69. (In Russ.) https://doi.org/10.17709/2410-1893-2023-10-4-5. EDN: NDLLNM

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ISSN 2410-1893 (Online)