Annexin A7 and Its Related Protein Suppressor of Death Domains Regulates Migration and Proliferation of Hca-P Cells
Objective: This study was to investigate whether annexin A7 (AnnexinA7, ANXA7) and its co-related protein tumor celldeath domain silencer [suppressor of death domains (SODD)] regulates the migratory phenotype of liver cancer cells.Materials and Methods: In this experimental study, expression of ANXA...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Royan Institute (ACECR), Tehran
2023-11-01
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Series: | Cell Journal |
Subjects: | |
Online Access: | https://www.celljournal.org/article_707712_e78556e367467e9fe7bbd2183ecc9891.pdf |
Summary: | Objective: This study was to investigate whether annexin A7 (AnnexinA7, ANXA7) and its co-related protein tumor celldeath domain silencer [suppressor of death domains (SODD)] regulates the migratory phenotype of liver cancer cells.Materials and Methods: In this experimental study, expression of ANXA7 in Hca-P cells, PANXA7 downregulatedcells and PANXA7 unrelated sequence cells was detected by real-time quantitative polymerase chainreaction (PCR) at mRNA level and western blotting at protein level. Transwell migration and invasion assayswere performed to determine the migratory phenotype.Results: After inhibition of ANXA7 expression, expression of SODD protein was also significantly decreased (P<0.05).Transwell cell transfer experiments showed that number of tumor cells that penetrated into the cell membrane wassignificantly reduced after ANXA7 silencing (P<0.05). Transwell cell invasion assay showed that number of tumorcells penetrating into Matrigel was significantly reduced after ANXA7 down-regulation (P<0.05). The CCK8 assay wasmeasured at 0, 24 and 48 hours, and proliferation rate of PANXA7 lower weir cells was slower than that of Hca-P cellsand PANXA7 non-related sequence cells (P<0.05).Conclusion: SODD expression was decreased with the down-regulation of ANXA7. Down-regulating ANXA7 in Hca-Pcells decreased proliferation, migration and invasion of tumor cells. |
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ISSN: | 2228-5806 2228-5814 |