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去甲基化上调p27Kip1使顺铂耐药的人卵巢癌细胞SKOV3致敏。

Upregulation of p27Kip1 by demethylation sensitizes cisplatin-resistant human ovarian cancer SKOV3 cells.

作者信息

Zhao Yan, Li Qiaoyan, Wu Xiaoying, Chen Puxiang

机构信息

Department of Gynecology and Obstetrics, The Maternal and Child Health Hospital of Hunan, Changsha, Hunan 410008, P.R. China.

Department of Gynecology and Obstetrics, Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, P.R. China.

出版信息

Mol Med Rep. 2016 Aug;14(2):1659-66. doi: 10.3892/mmr.2016.5399. Epub 2016 Jun 14.

Abstract

Ovarian cancer has a poor prognosis due to its chemoresistance, and p27Kip1 (p27) has been implicated in tumor prognosis and drug-resistance. However, the regulatory mechanisms of p27 in drug‑resistance in ovarian cancer remain unknown. The current study successfully established chemoresistant cell lines using paclitaxel (TAX), cisplatin (DDP) and carboplatin (CBP) in SKOV3 ovarian cancer cells. The results indicated that the expression levels of p27 were dramatically downregulated in chemoresistant cells. However, 5-aza-2'-deoxycytidine (5-aza) treatment restored p27 expression in DDP-resistant cells, and increased their sensitivity to DDP. In addition, it was observed that the methylation of DDP‑resistant cells, which was downregulated by 5‑aza treatment, was significantly higher compared with SKOV3 cells. Additionally, the overexpression of p27 arrested the cell cycle in S phase and promoted an apoptotic response to DDP. In conclusion, p27 was involved in chemoresistance of SKOV3 cells. Upregulated p27 expression induced by demethylation may enhance sensitivity to DDP through the regulation of the cell cycle.

摘要

卵巢癌因其化疗耐药性而预后较差,并且p27Kip1(p27)与肿瘤预后和耐药性有关。然而,p27在卵巢癌耐药中的调控机制仍不清楚。当前研究成功地在SKOV3卵巢癌细胞中使用紫杉醇(TAX)、顺铂(DDP)和卡铂(CBP)建立了化疗耐药细胞系。结果表明,p27的表达水平在化疗耐药细胞中显著下调。然而,5-氮杂-2'-脱氧胞苷(5-aza)处理恢复了顺铂耐药细胞中p27的表达,并增加了它们对顺铂的敏感性。此外,观察到5-aza处理下调的顺铂耐药细胞的甲基化水平与SKOV3细胞相比显著更高。另外,p27的过表达使细胞周期停滞在S期,并促进了对顺铂的凋亡反应。总之,p27参与了SKOV3细胞的化疗耐药。去甲基化诱导的p27表达上调可能通过调节细胞周期增强对顺铂的敏感性。

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