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四氧化二砷和顺铂诱导宫颈癌细胞凋亡协同作用。

Tetraarsenic oxide and cisplatin induce apoptotic synergism in cervical cancer.

机构信息

Department of Obstetrics and Gynecology, Busan Paik Hospital, Inje University, Busan 614-735, Republic of Korea.

出版信息

Oncol Rep. 2013 Apr;29(4):1540-6. doi: 10.3892/or.2013.2243. Epub 2013 Jan 18.

DOI:10.3892/or.2013.2243
PMID:23338680
Abstract

Tetraarsenic oxide (As4O6, TAO) is a new arsenic compound that inhibits cell growth and induces apoptosis in human cervical cancer cell lines. In the present study, we report that the growth of tumor cells (CaSki) was inhibited by treatment with TAO alone or in combination with cisplatin or paclitaxel in vitro and in vivo. Proliferation was assessed by WST-1 assay, and apoptosis was assessed by Annexin-V/PI FACS analysis in the CaSki cell line treated with a single agent or with the combinations of two agents. Expression of apoptosis-related proteins was analyzed by western blot analysis. A mouse xenograft model using CaSki cells was used to determine the in vivo activity of tetraarsenic oxide alone and in combination with cisplatin or paclitaxel by estimation of tumor size. At the end of the experiment, tumor tissue from each mouse was removed and processed for TUNEL analysis for confirmation of apoptotic cells. TAO was able to inhibit cell proliferation in a time- and dose-dependent manner. A combination of TAO and cisplatin effectively induced apoptosis by activating caspase-3. Using a mouse xenograft model, the sizes of tumors which were treated with a single agent and with a combination of agents decreased in a time-dependent manner. A combination of TAO and cisplatin resulted in a significantly reduced tumor size (P<0.05). The data for the histochemical staining of TUNEL-positive cells showed that the number of apoptotic cells was significantly increased by the combination of TAO and cisplatin. Thus, TAO is a good candidate for use in a combined regimen with cisplatin for patients with cervical cancer.

摘要

四氧化二砷(As4O6,TAO)是一种新型砷化合物,可抑制人宫颈癌系细胞的生长并诱导其凋亡。本研究报道,TAO 单独或与顺铂或紫杉醇联合应用于体外和体内均可抑制肿瘤细胞(CaSki)的生长。采用 WST-1 法检测细胞增殖,采用 Annexin-V/PI FACS 分析法检测单独用药或联合用药后 CaSki 细胞系的细胞凋亡。采用 Western blot 分析法分析凋亡相关蛋白的表达。采用 CaSki 细胞建立小鼠异种移植模型,通过测定肿瘤大小来确定 TAO 单独及与顺铂或紫杉醇联合的体内活性。实验结束时,从每只小鼠中取出肿瘤组织并进行 TUNEL 分析以确认凋亡细胞。TAO 能够以时间和剂量依赖的方式抑制细胞增殖。TAO 与顺铂联合可通过激活 caspase-3 有效诱导细胞凋亡。采用小鼠异种移植模型,单独及联合用药组肿瘤的大小均随时间呈依赖性减小。TAO 与顺铂联合可显著减小肿瘤体积(P<0.05)。TUNEL 阳性细胞的组织化学染色数据表明,TAO 与顺铂联合可显著增加凋亡细胞数量。因此,TAO 是联合顺铂治疗宫颈癌患者的候选药物。

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