| Autor: |
ZHANG Lei, LIU Hao, JIN Ping, ZHANG Ke, WANG Xiaomei, ZHAO Yingying |
| Jazyk: |
čínština |
| Rok vydání: |
2018 |
| Předmět: |
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| Zdroj: |
Zhongliu Fangzhi Yanjiu, Vol 45, Iss 6, Pp 371-375 (2018) |
| Druh dokumentu: |
article |
| ISSN: |
1000-8578 |
| DOI: |
10.3971/j.issn.1000-8578.2018.17.0562 |
| Popis: |
Objective To investigate the inhibition effect of paclitaxel combined with SAHA on the proliferation of human cervical cancer HeLa cells in vitro and related mechanism. Methods Human cervical cancer HeLa cells were treated with paclitaxel (10 nmol/L), SAHA (10 μmol/L), and paclitaxel (10 nmol/L)+SAHA (10 μmol/L) separately for 24h or 48h. The inhibitory rate of tumor cells was determined by MTT assay. Flow cytometry was used to detect HeLa cells apoptosis and cell cycles. Results MTT assay showed that the proliferation inhibitory rates of the combination group after 24h or 48h treatment were significantly higher than those of paclitaxel and SAHA groups, moreover, paclitaxel and SAHA had overlapping effects (Q=0.861, Q=1.25). SAHA combined with paclitaxel could significantly increase the apoptotic rate of HeLa cells than SAHA or paclitaxel alone. HeLa cells were randomly in G0/G1 phase after SAHA and paclitaxel treatment for 24h, which suggested that SAHA combined with paclitaxel could significantly inhibit DNA synthesis and replication during HeLa cell mitosis. Conclusion The combination of SAHA and paclitaxel could significantly induce cervical cancer HeLa cells apoptosis, inhibit cell proliferation, block cell cycle and enhance their anti-tumor ability. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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