Increasing of malignancy of breast cancer cells after cryopreservation: molecular detection and activation of angiogenesis after CAM-xenotransplantation

• Published in: BMC cancer 2020-08, Vol.20 (1), p.753-753, Article 753
• Main Authors: Du, Xinxin, Todorov, Plamen, Isachenko, Evgenia, Rahimi, Gohar, Mallmann, Peter, Meng, Yuanguang, Isachenko, Vladimir
• Format: Article
• Language: English
• Subjects: Actin; Actins - metabolism; Angiogenesis; Antibodies; Breast cancer; Breast Neoplasms - blood supply; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cadherins - metabolism; Cancer cells; Cell Adhesion; Cell adhesion & migration; Cell culture; Cell cycle; Cell growth; Cell Line, Tumor; Cell Movement; Cell Proliferation; Cell Shape; Cholecystokinin; Chorioallantoic membrane; Collagen; Comparative analysis; Computer aided manufacturing; Cryopreservation; Cryopreservation - methods; Cytology; E-cadherin; Epithelial-Mesenchymal Transition; Female; Filopodia; Freezing; GATA-3 protein; GATA3 Transcription Factor - metabolism; Humans; Ki-67 Antigen - metabolism; Lamellipodia; Malignancy; Mesenchyme; Metastases; Metastasis; Morphology; Muscle proteins; Neoplasm Invasiveness; Neoplasm Proteins - metabolism; Neovascularization, Pathologic - etiology; Ovaries; p53 Protein; Phenotype; Phenotypes; Sucrose; Thawing; Transplantation; Transplantation, Heterologous; Tumor proteins; Tumor Suppressor Protein p53 - metabolism; Vimentin; Vimentin - metabolism; Western blotting; Wound healing; Xenografts
• ISSN: 1471-2407; 1471-2407
• DOI: 10.1186/s12885-020-07227-z

Ovarian tissue cryopreservation has a wide range of cancerous indications. Avoiding relapse becomes a specific concern that clinicians frequently encounter. The data about the comparative viability of cancer cells after cryopreservation are limited. This study aimed to evaluate the effect of cryopreservation on breast cancer cells. We used in-vitro cultured ZR-75-1 and MDA-MB-231 cell lines. Cell samples of each lineage were distributed into the non-intervened and cryopreserved groups. The cryopreservation procedures comprised programmed slow freezing followed by thawing at 100 °C, 60 s. Biological phenotypes and the related protein markers were compared between the two groups. The EVOS FL Auto 2 Cell Image System was used to monitor cell morphology. Cell proliferation, motility, and penetration were characterized by CCK-8, wound-healing, and transmembrane assay, respectively. The expression of Ki-67, P53, GATA3, E-cadherin, Vimentin, and F-Actin was captured by immunofluorescent staining and western blotting as the proxy measurements of the related properties. The chorioallantoic membrane (CAM) xenotransplantation was conducted to explore angiogenesis induced by cancer cells. After 5 days in vitro culture, the cell concentration of cryopreserved and non-intervened groups was 15.7 × 10 vs. 14.4 × 10 cells/ml, (ZR-75-1, p > 0.05), and 25.1 × 10 vs. 26.6 × 10 cells/ml (MDA-MB-231, p > 0.05). Some cryopreserved ZR-75-1 cells presented spindle shape with filopodia and lamellipodia and dissociated from the cell cluster after cryopreservation. Both cell lines demonstrated increased cell migrating capability and invasion after cryopreservation. The expression of Ki-67 and P53 did not differ between the cryopreserved and non-intervened groups. E-cadherin and GATA3 expression downregulated in the cryopreserved ZR-75-1 cells. Vimentin and F-actin exhibited an upregulated level in cryopreserved ZR-75-1 and MDA-MB-231 cells. The cryopreserved MDA-MB-231 cells induced significant angiogenesis around the grafts on CAM with the vascular density 0.313 ± 0.03 and 0.342 ± 0.04, compared with that of non-intervened cells of 0.238 ± 0.05 and 0.244 ± 0.03, p < 0.0001. Cryopreservation promotes breast cancer cells in terms of epithelial-mesenchymal transition and angiogenesis induction, thus increasing metastasis risk.