Skip to main content
Log in

An Unusual Pathway of Mitoptosis Found in Ehrlich Carcinoma Cells

  • GENERAL BIOLOGY
  • Published:
Doklady Biological Sciences Aims and scope Submit manuscript

Abstract

An integrated microscopic study of the destruction of mouse Ehrlich ascites carcinoma (EAC) cells under starvation conditions has been carried out. It has been found that, in addition to apoptosis, necrosis, and apoptotic necrosis, already known for EAC, cell destruction can also occur through mitochondrial autolysis, which is proposed to be considered a new kind of mitoptosis. A mitoptosis in EAC is characterized by the appearance of many autolyzing mitochondria, the fusion of which leads to rupture of the cell membrane and the ejection of the nucleus from the cell. It is assumed that the polymorphism of EAC destruction patterns is explained by the different physiological state of the cells, which determines the “choice” of the cell death mechanism. This situation poses a challenge for researchers to develop complex inducers with the ability to stimulate all possible types of cancer cell death.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.

Similar content being viewed by others

REFERENCES

  1. Bruin, D.E.C. and Medema, J.P., Cancer Treat. Rev., 2008, vol. 34, pp. 737–749. https://doi.org/10.1016/j.ctrv.2008.07.001

    Article  PubMed  Google Scholar 

  2. Rufini, A. and Melino, G., Biochem. Biophys. Res. Commun., 2011, vol. 414, pp. 445–450. https://doi.org/10.1016/j.bbrc.2011.09.110

    Article  CAS  PubMed  Google Scholar 

  3. Dimou, A., Syrigos, N.K., and Saif, M.W., Ther. Adv. Med. Oncol., 2012, vol. 4, pp. 271–279. https://doi.org/10.1177/1758834012446008

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Moriwaki, K. and Chan, F.K.M., Genes Dev., 2013, vol. 27, pp. 1640–1649. https://doi.org/10.1101/gad.223321.113

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Cho, Y.S. and Park, S.Y., Biomol. Ther., 2014, vol. 22, pp. 167–175. https://doi.org/10.4062/biomolther.2014.046

    Article  CAS  Google Scholar 

  6. Osorio-Vega, H., Finol, H.J., Roschman-Gonzalez, A., et al., Acta Microsc., 2016, vol. 25, pp. 65–70.

    Google Scholar 

  7. Reunov, A.A., Reunov, A.V., Pimenova, E.A., et al., Gene, 2018, vol. 658, pp. 1–9. https://doi.org/10.1016/j.gene.2018.03.012

    Article  CAS  PubMed  Google Scholar 

  8. Ozaslan, M., Karagoz, I.D., Kilic, I.H., et al., Afr. J. Biotechnol., 2011, vol. 10, pp. 2375–2378. https://doi.org/10.5897/AJBx10.017

    Article  Google Scholar 

  9. Da Mota, M.F., Benfica, P.L., Batista, A.C., et al., J. Ethnopharmacol., 2012, vol. 139, pp. 319–329. https://doi.org/10.1016/j.jep.2011.04.055

    Article  PubMed  Google Scholar 

  10. Osman, A.M.M., Alqahtani, A.A., Damanhouri, Z.A., et al., Cancer Cell Int., 2015, vol. 15, pp. 104–117. https://doi.org/10.1186/s12935-015-0258-1

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Menchinskaya, E.S., Pislyagin, E.A., Kovalchyk, S.N., et al., Chemotherapy, 2013, vol. 59, pp. 181–191. https://doi.org/10.1159/000354156

    Article  CAS  PubMed  Google Scholar 

  12. Reunov, A.A., Reunov, A.V., Pimenova, E.A., et al., RAS Rep. Biol. Sci., 2015, vol. 462, pp. 161–163. https://doi.org/10.1134/S0012496615020040

    Article  CAS  Google Scholar 

  13. Chaabane, W., User, S.D., El-Gazzah, M., et al., Arch. Immunol. Ther. Exp., 2013, vol. 61, pp. 43–58. https://doi.org/10.1007/s00005-012-0205-y

    Article  CAS  Google Scholar 

  14. Jangamreddy, J.R. and Los, M.J., Hepat. Mon., 2012, vol. 12, e6159. https://doi.org/10.5812/hepatmon.6159

    Article  PubMed  PubMed Central  Google Scholar 

  15. Lyamzaev, K.G., Nepryakhina, O.K., Saprunova, V.B., et al., Biochim. Biophys. Acta, 2008, vol. 1777, pp. 817–825. https://doi.org/10.1016/j.bbabio.2008.03.027

    Article  CAS  PubMed  Google Scholar 

Download references

ACKNOWLEDGMENTS

We are grateful to D.V. Fomin for the help in using the equipment of the Center for Shared Use of the NSCMB FEB, Russian Academy of Sciences (Vladivostok, Russia). Part of the study was carried out at the Electron Microscopy Laboratory of the University of St. Francis Xavier (Antigonish, Nova Scotia, Canada).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to E. A. Pimenova.

Ethics declarations

Conflict of interests. The authors declare that they have no conflict of interest.

Statement on the welfare of animals. All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.

Additional information

Translated by I. Shipounova

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pimenova, E.A., Reunova, Y.A., Menchinskaya, E.S. et al. An Unusual Pathway of Mitoptosis Found in Ehrlich Carcinoma Cells. Dokl Biol Sci 494, 240–243 (2020). https://doi.org/10.1134/S0012496620050063

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0012496620050063

Keywords:

Navigation