Xiaoaiping combined with cisplatin can inhibit proliferation and invasion and induce cell cycle arrest and apoptosis in human ovarian cancer cell lines
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作者:
Zheng, Ai-Wen
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Zhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R ChinaZhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
Zheng, Ai-Wen
[1
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Chen, Ya-Qing
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Zhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R ChinaZhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
Chen, Ya-Qing
[1
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Fang, Jing
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Zhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R ChinaZhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
Fang, Jing
[1
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Zhang, Ying-Li
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Zhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R ChinaZhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
Zhang, Ying-Li
[1
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Jia, Dong-Dong
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Zhejiang Canc Hosp, Dept Bone & Soft Tissue Surg, 1 Banshan East Rd, Hangzhou 310022, Zhejiang, Peoples R ChinaZhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
Jia, Dong-Dong
[2
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机构:
[1] Zhejiang Canc Hosp, Dept Gynecol Oncol, Hangzhou 310022, Zhejiang, Peoples R China
[2] Zhejiang Canc Hosp, Dept Bone & Soft Tissue Surg, 1 Banshan East Rd, Hangzhou 310022, Zhejiang, Peoples R China
Purpose: The aim of the present study was utilizing Xiaoaiping as a single agent or combined with cisplatin to study its effect on the ovarian cancer cells (HO-8910 and HO-8910PM cells) in tumor cell proliferation, cell apoptosis, cell cycle distribution and cell invasion and migration. Methods: Both HO-8910 and HO-8910PM cell lines were treated with Xiaoaiping injection, cisplatin or combination. Effects on the cell viability and apoptosis induction were estimated using the Cell counting Kit-8 assay and Annexin V-FITC/Propidium Iodide staining. The distribution of cells in different phases of the cell cycle was assayed using flow cytometry analysis. The effects of Xiaoaiping on the inhibition of cell invasion and migration were researched with Transwell cell migration. Results: Both Xiaoaiping and cisplatin significantly decreased the HO-8910 cell survival versus control arm. Combination treatment showed a higher cytotoxicity to cells in vitro than Xiaoaiping and cisplatin alone. An increase in the G0/G1 phase fraction in HO-8910 cells treated with either Xiaoaiping or cisplatin alone was evident when compared to the fraction in control arm. Compared to the effects of treatment with either agent alone, combination treatment significantly increased the fraction of cells in G0/G1 phase. The HO-8910 cell lines treated with cisplatin demonstrated a significant increase of apoptotic cell rate compared to untreated cell lines. The rate of apoptosis in combined treatment group was significantly higher than that of the single agent treatment groups. A significant reduction in the number of invading cells was observed for Xiaoaiping-treated HO-8910 cells compared with the control group. However, cisplatin did not significantly induce the migration of cells versus untreated cells. Combination of Xiaoaiping and cisplatin significantly suppressed cell invasion and migration versus single-drug treatment in HO-8910 cells. The results of HO-8910PM cells were similar with HO-8910 cells in all tests. Conclusions: In summary, our results showed that Xiaoaiping as a single agent or combined with cisplatin could induce cell cycle arrest, cause apoptosis and necrosis in ovarian cancer cells, and inhibit cell invasion and migration. The present study also laid a foundation for further investigation involving molecular mechanism. Above all, it may provide a novel therapeutic regimen for ovarian cancer. (C) 2017 Elsevier Masson SAS. All rights reserved.
机构:
Univ Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
Gloria, Nathalie Fonseca
Soares, Nathalia
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Univ Fed Rio de Janeiro, Inst Biomed Sci, Lab Cell Proliferat & Differentiat, Rio De Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
Soares, Nathalia
Brand, Camila
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Univ Fed Rio de Janeiro, Inst Biomed Sci, Lab Cell Proliferat & Differentiat, Rio De Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
Brand, Camila
Oliveira, Felipe Leite
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Univ Fed Rio de Janeiro, Inst Biomed Sci, Lab Cell Proliferat & Differentiat, Rio De Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
Oliveira, Felipe Leite
Borojevic, Radovan
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Excell Biomed Serv, Rio De Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
Borojevic, Radovan
Teodoro, Anderson Junger
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Univ Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, BrazilUniv Fed Estado Rio de Janeiro, Lab Nutr Biochem, Program Food & Nutr, Rio de Janeiro, Brazil
机构:
Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Urol, Xian, Shaanxi, Peoples R ChinaXi An Jiao Tong Univ, Affiliated Hosp 1, Dept Urol, Xian, Shaanxi, Peoples R China
Chong, Yue
Xue, Li
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Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Urol, 157 Xiwulu Rd, Xian 710004, Shaanxi, Peoples R ChinaXi An Jiao Tong Univ, Affiliated Hosp 1, Dept Urol, Xian, Shaanxi, Peoples R China