Changes in survivin messenger RNA level during chemotherapy treatment in ovarian cancer cells

被引:37
作者
Wang, ZH [1 ]
Xie, YH [1 ]
Wang, HB [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tonji Med Coll, Dept Obstet & Gynecol, Uni Hosp, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; ovarian cancer; Survivin; Mdr1; Taxol; platinum; RT-PCR;
D O I
10.4161/cbt.4.7.1782
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To investigate the role of antiapoptosis gene, survivin involved in regulating cell sensitivity to taxanes and platinum compounds. Methods: Cultured human epithelial ovarian cancer cell line A2780 and its platinum (DDP)- resistance cell line A2780/ DDP were divided into three groups as control, treatment with DDP, and treatment with Taxol Expression of mdr1 and survivin genes in each group was detected by using Reverse transcription- polymerase chain reaction ( RT- PCR). Apoptosis in the ovarian cancer cell lines was measured by flow cytometry. Results: After treatment with DDP for 48 h, relative survivin expression was significantly lower than that of no drug given (p < 0.05). In A2780/ DDP cells, expression of Survivn was obviously higher than that of the control group (P < 0.05) after treatment of DDP for 48 h. Interestingly, survivin mRNA level was significantly decreased after treatment with Taxol for 48h in the A2780/DDP-Taxol group compared with that in the control group. Apoptosis rate of A2780 cells was significantly increased to 46.21% and 44.46%, respectively, with treatment of DDP and Taxol. However, apoptosis rate in A2780/ DDP was only 20.04% after DDP treatment for 48 h, demonstrating the presence of resistance to DDP in A2780/ DDP cells. Conclusions: This study demonstrated that changes in survivin mRNA level were related to the chemotherapy- induced apoptosis. Survivin may be considered as a biological indicator of the chemo- resistance of ovarian cancer.
引用
收藏
页码:716 / 719
页数:4
相关论文
共 28 条
[1]   Molecular circuits of apoptosis regulation and cell division control: The survivin paradigm [J].
Altieri, DC .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 92 (04) :656-663
[2]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[3]   P-glycoprotein: from genomics to mechanism [J].
Ambudkar, SV ;
Kimchi-Sarfaty, C ;
Sauna, ZE ;
Gottesman, MM .
ONCOGENE, 2003, 22 (47) :7468-7485
[4]  
CHRISTIAN MC, 1994, GYNECOL ONCOL S, V55, P143
[5]   Chemotherapy resistance in ovarian cancer: New molecular perspectives [J].
Coukos, G ;
Rubin, SC .
OBSTETRICS AND GYNECOLOGY, 1998, 91 (05) :783-792
[6]   Survivin expression in ovarian cancer and its correlation with clinico-pathological, surgical and apoptosis-related parameters [J].
Ferrandina, G ;
Legge, F ;
Martinelli, E ;
Ranelletti, FO ;
Zannoni, GF ;
Lauriola, L ;
Gessi, M ;
Gallotta, V ;
Scambia, G .
BRITISH JOURNAL OF CANCER, 2005, 92 (02) :271-277
[7]   Apoptosis-based evaluation of chemosensitivity in ovarian cancer patients [J].
Flick, MB ;
O'Malley, D ;
Rutherford, T ;
Rodov, S ;
Kamsteeg, M ;
Hao, XY ;
Schwartz, P ;
Kacinski, BM ;
Mor, G .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2004, 11 (04) :252-259
[8]  
Gadducci A, 2002, EUR J GYNAECOL ONCOL, V23, P390
[9]   Expression of survivin mRNA and protein in gastric cancer cell line (MKN-45) during cisplatin treatment [J].
Ikeguchi, M ;
Liu, J ;
Kaibara, N .
APOPTOSIS, 2002, 7 (01) :23-29
[10]   Cancer statistics, 2002 [J].
Jemal, A ;
Thomas, A ;
Murray, T ;
Thun, M .
CA-A CANCER JOURNAL FOR CLINICIANS, 2002, 52 (01) :23-47