Preview

Advances in Molecular Oncology

Advanced search

Signs of apoptosis in circulating tumor cell subpopulations with phenotypes associated with stemness and epithelial-mesenchymal transition in breast carcinoma

https://doi.org/10.17650/2313-805X-2022-9-4-96-111

Abstract

Introduction. Ability of circulating tumor cells (CTC) initiate metastases in distant sites is associated primarily with their resistance to apoptosis which allows them to retain viability in the blood. Knowledge of phenotypical signs associated with this ability would allow to predict the risk of metastases and optimize adjuvant therapy.
Aim. To examine signs of apoptosis in CTC populations with various phenotypical characteristics.
Materials and methods. The study included 58 patients with invasive breast carcinoma of unspecified type, stages T1–4N0–3M0. Cell concentrates extracted from patients’ whole blood were stained with an antibody cocktail against CK7 / 8, CD45, EpCAM, CD44, CD24, CD133, ALDH, N-cadherin which allowed to identify CTC with signs of stemness and epithelial-mesenchymal transition. Annexin V and 7‑amino-actinomycin D staining was used for evaluation of apoptosis stage in CTC populations.
Results. Circulating tumor cells are characterized by heterogeneity in respect to signs of stemness and epithelial-mesenchymal transition and presence of early and late signs of apoptosis and necrosis. CTC phenotypes including co-expression of epithelial marker CK7 / 8 and stemness marker CD133 (but not CD44) are characterized by absence of signs of apoptosis. Co-expression of CK7 / 8 and CD133 in CTC with stemness markers CD44+ / C D24– is associated with development of early but not late signs of apoptosis and necrosis. Circulating tumor cells without co-expression of CK7 / 8 and CD133 could have both early and late signs of apoptosis and necrosis. Circulating tumor cells phenotypes with signs of early apoptosis expressing CD133 remain in blood after non-adjuvant chemotherapy opposed to CTC without CD133 expression.
Conclusion. There are CTC phenotypical signs associated with stemness and epithelial-mesenchymal transition and linked to apoptosis resistance or sensitivity.

About the Authors

V. M. Perelmuter
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

Vladimir Mikhailovich Perelmuter

5 Cooperative Lane, Tomsk 634009



E. S. Grigorieva
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

5 Cooperative Lane, Tomsk 634009



M. V. Zavyalova
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences; Siberian State Medical University, Ministry of Health of Russia
Russian Federation

5 Cooperative Lane, Tomsk 634009

2 Moskovsky Tract, Tomsk 634050



L. A. Tashireva
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

5 Cooperative Lane, Tomsk 634009



V. V. Alifanov
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences; Siberian State Medical University, Ministry of Health of Russia
Russian Federation

5 Cooperative Lane, Tomsk 634009

2 Moskovsky Tract, Tomsk 634050



O. E. Saveleva
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

5 Cooperative Lane, Tomsk 634009



S. V. Vtorushin
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences; Siberian State Medical University, Ministry of Health of Russia
Russian Federation

5 Cooperative Lane, Tomsk 634009

2 Moskovsky Tract, Tomsk 634050



E. L. Choynzonov
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences; Siberian State Medical University, Ministry of Health of Russia
Russian Federation

5 Cooperative Lane, Tomsk 634009

2 Moskovsky Tract, Tomsk 634050



N. V. Cherdyntsevа
Cancer Research Institute of the Tomsk National Research Medical Center of the Russian Academy of Sciences; Siberian State Medical University, Ministry of Health of Russia; National Research Tomsk State University
Russian Federation

5 Cooperative Lane, Tomsk 634009

2 Moskovsky Tract, Tomsk 634050

36 Lenin Prospekt, Tomsk 634050



References

1. Vismara M., Reduzzi C., Daidone M.G. et al. Circulating tumor cells (CTCs) heterogeneity in metastatic breast cancer: different approaches for different needs. Adv Exp Med Biol 2020;1220: 81–91. DOI: 10.1007/978-3-030-35805-1_6

2. Savelieva O.E., Tashireva L.A., Buldakov M.A. et al. CXCR4 expression in different subsets of CTCs and single (detached) breast cancer cells. Sibirskij onkologicheskij zhurnal = Siberian Journal of Oncology 2018;17(4):75–80. (In Russ.). DOI: 10.21294/1814-4861-2018-17-4-75-80

3. Krog B.L., Henry M.D. Biomechanics of the circulating tumor cell microenvironment. Adv Exp Med Biol 2018;1092:209–33. DOI: 10.1007/978-3-319-95294-9_11

4. Meng S., Tripathy D., Frenkel E.P. et al. Circulating tumor cells in patients with breast cancer dormancy. Clin Cancer Res 2004;10(24):8152–62. DOI: 10.1158/1078-0432.CCR-04-1110

5. Aceto N., Bardia A., Miyamoto D.T. et al. Circulating tumor cell clusters are oligoclonal precursors of breast cancer metastasis. Cell 2014;158(5):1110–22. DOI: 10.1016/j.cell.2014.07.013

6. Weinberg R.A. Leaving home early: reexamination of the canonical models of tumor progression. Cancer Cell 2008;14(4):283–4. DOI: 10.1016/j.ccr.2008.09.009

7. Buchheit C.L., Weigel K.J., Schafer Z.T. Cancer cell survival during detachment from the ECM: multiple barriers to tumour progression. Nat Rev Cancer 2014;14(9):632–41. DOI: 10.1038/nrc3789

8. Yu T., Wang C., Xie M. et al. Heterogeneity of CTC contributes to the organotropism of breast cancer. Biomed Pharmacother 2021;137:111314. DOI: 10.1016/j.biopha.2021.111314

9. Barzegar Behrooz A., Syahir A., Ahmad S. CD133: beyond a cancer stem cell biomarker. J Drug Target 2019;27(3):257–69. DOI: 10.1080/1061186X.2018.1479756

10. Guo F., Yang Z., Sehouli J. et al. Blockade of ALDH in cisplatinresistant ovarian cancer stem cells in vitro synergistically enhances chemotherapy-induced cell death. Curr Oncol 2022;29(4):2808–22. DOI: 10.3390/curroncol29040229

11. Chen C., Zhao S., Karnad A. et al. The biology and role of CD44 in cancer progression: therapeutic implications. J Hematol Oncol 2018;11(1):64. DOI: 10.1186/s13045-018-0605-5

12. Cao Z.-Q., Wang Z., Leng P. Aberrant N-кадгерин expression in cancer. Biomed Pharmacother 2019;118:109320. DOI: 10.1016/j.biopha.2019.109320

13. Jordan N.V., Bardia A., Wittner B.S. et al. HER2 expression identifies dynamic functional states within circulating breast cancer cells. Nature 2016;537(7618):102–6. DOI: 10.1038/nature19328

14. Kallergi G., Konstantinidis G., Markomanolaki H. et al. Apoptotic circulating tumor cells in early and metastatic breast cancer patients. Mol Cancer Ther 2013;12(9):1886–95. DOI: 10.1158/1535-7163.MCT-12-1167

15. Spiliotaki M., Mavroudis D., Kapranou K. et al. Evaluation of proliferation and apoptosis markers in circulating tumor cells of women with early breast cancer who are candidates for tumor dormancy. Breast Cancer Res;16(6):485. DOI: 10.1186/s13058-014-0485-8

16. Jansson S., Bendahl P.O., Larsson A.M. et al. Prognostic impact of circulating tumor cell apoptosis and clusters in serial blood samples from patients with metastatic breast cancer in a prospective observational cohort. BMC Cancer 2016;16:433. DOI: 10.1186/s12885-016-2406-y

17. Pandya V., Githaka J.M., Patel N. et al. BIK drives an aggressive breast cancer phenotype through sublethal apoptosis and predicts poor prognosis of ER-positive breast cancer. Cell Death Dis 2020;11(6):448. DOI: 10.1038/s41419-020-2654-2

18. Xu Y., So C., Lam H.M. et al. Flow cytometric detection of newlyformed breast cancer stem cell-like cells after apoptosis reversal. J Vis Exp 2019;143. DOI: 10.3791/58642

19. Zimmermann M., Meyer N. Annexin V/7-AAD staining in keratinocytes. Methods Mol Biol 2011;740:57–63. DOI: 10.1007/978-1-61779-108-6_8

20. Madjd Z., Mehrjerdi A.Z., Sharifi A.M. et al. CD44+ cancer cells express higher levels of the anti-apoptotic protein Bcl-2 in breast tumours. Cancer Immun 2009;9:4.

21. Mori Y., Takeuchi A., Miyagawa K. et al. CD133 prevents colon cancer cell death induced by serum deprivation through activation of Akt-mediated protein synthesis and inhibition of apoptosis. FEBS Open Bio 2021;11(5):1382–94. DOI: 10.1002/2211-5463.13145

22. Nguyen P.T., Nguyen D., Chea C. et al. Interaction between N-cadherin and decoy receptor-2 regulates apoptosis in head and neck cancer. Oncotarget 2018;9(59):31516–30. DOI: 10.18632/oncotarget.25846

23. Xu Y., So C., Lam H.M. et al. Apoptosis reversal promotes cancer stem cell-like cell formation. Neoplasia 2018;20(3):295–303. DOI: 10.1016/j.neo.2018.01.005


Review

For citations:


Perelmuter V.M., Grigorieva E.S., Zavyalova M.V., Tashireva L.A., Alifanov V.V., Saveleva O.E., Vtorushin S.V., Choynzonov E.L., Cherdyntsevа N.V. Signs of apoptosis in circulating tumor cell subpopulations with phenotypes associated with stemness and epithelial-mesenchymal transition in breast carcinoma. Advances in Molecular Oncology. 2022;9(4):96‑111. (In Russ.) https://doi.org/10.17650/2313-805X-2022-9-4-96-111

Views: 377


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2313-805X (Print)
ISSN 2413-3787 (Online)