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塞来昔布对顺铂抑制子宫颈癌HeLa细胞的增效作用 被引量:1

Enhancing effect of celecoxib on the anti-proliferative effect of cisplatin against human cervical carcinoma HeLa cells
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摘要 目的探讨塞来昔布与顺铂联用对抑制人类子宫颈癌HeLa细胞的增效作用及其可能机制。方法用四唑盐比色法(MTT)观察塞来昔布与顺铂单独和联用对HeLa细胞的生长抑制情况,流式细胞术(FCM)检测单用塞来昔布、顺铂以及二者联合使用时HeLa细胞的凋亡率和细胞周期变化。结果塞来昔布对子宫颈癌HeLa细胞的抑制作用呈浓度和时间依赖性。塞来昔布与顺铂联合应用后对子宫颈癌HeLa细胞的抑制作用较单独用药显著增强(P=0.000),两者有协同或相加作用。塞来昔布(50μmol/L)及顺铂(16μmol/L)均可有效诱导HeLa细胞凋亡,联用凋亡率明显增加,细胞周期发生变化,表现为G0/G1期增加,S期减少。结论塞来昔布与顺铂联用对HeLa细胞有协同抗肿瘤效应。 Objective To investigate the enhancing effect of Celecoxib on the anti-proliferative effect of cisplatin (DDP) against human cervical carcinoma HeLa cells and to explore the possible mechanism. Methods After treatment of HeLa cells with Celecoxib or/and DDP, the growth suppression of HeLa cells was measured by MTT assay. Cell cycle and apoptosis were examined by flow cytometry. Results The inhibition of Celecoxib on HeLa cells was dose-dependent and time-dependent.The inhibitory effect was remarkable enhanced in asynergistic or additive pattern after treatment with the combination of Celecoxib and DDP (P =0.000) . Celecoxib (50 μmol/L) and DDP (16μmol/L) could respectively induce the apoptosis of HeLa cells and this effect of apoptosis induction was increased when combinated Celecoxib with DDP. They could change cell cycle of HeLa cells lines with G0/G1 phase cells increasing and S phase cells decreasing. Conclusion Celecoxib combined with DDP shows synergistic anti-tumor effects.
出处 《肿瘤研究与临床》 CAS 2009年第12期803-805,809,共4页 Cancer Research and Clinic
关键词 子宫颈肿瘤 药物疗法 联合 HELA细胞 塞来昔布 顺铂 Uterine cervical neoplasms Drug therapy, combination HeLa cells Celecoxib Cisplatin
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  • 1朱风尚,陈锡美,朱国英,王志荣,王毅军,张霞.特异性环氧合酶抑制剂对胃癌细胞BGC-823生长的影响[J].同济大学学报(医学版),2005,26(1):21-25. 被引量:4
  • 2朱风尚,陈锡美,王毅军,张霞,冯久贤.特异性环氧合酶抑制剂和抗癌药联用对胃癌细胞增殖的影响[J].中华肿瘤杂志,2007,29(3):186-188. 被引量:15
  • 3Patel VA, Dunn MJ, Sorokin A. Regulation of MDR - 1 ( P - glycoprorein) by cyclooxygenase-2 [J]. J Biol Chem, 2002; 277: 38915- 38920.
  • 4Sugawara I. Expression and functions of P - glycoprotein ( mdrl gene product) in normal and malignant tissues [ J]. Acta Pathol Jpn, 1990; 40 : 545 - 553.
  • 5Hirose M, Hosoi E, Hamano S, et al. Multidrug resistance in hematological malignancy [J]. J Med Invest, 2003; 50:126 - 135.
  • 6Tomonaga M, Oka M, Narasaki F, et al. The multidrug resistance - associated protein gene confers drug resistance in human gastric and colon cancers [J]. Jpn J Cancer Res, 1996; 87:1263 - 1270.
  • 7戴体俊.协同、拮抗等定义亟待统一[J]生理科学进展,1997(04).
  • 8江明性.药理学[M]人民卫生出版社,1989.
  • 9陈高明,李春海,程国钧,田方,孙丽亚,祝华,卞丽红,王红丽.肿瘤耐药相关标志在恶性肿瘤中的表达及意义[J].中华检验医学杂志,2000,23(1):19-22. 被引量:9

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  • 1Foulkes WD, Smith IE, Reis-Filhe JS. Triple-negative breast cancer. N Engl J Med, 2010, 363: 1938-1948.
  • 2Dawood S. Triple-negative breast cancer: epidemiology and management options. Drugs, 2010, 70: 2247-2258.
  • 3Rastelli F, Biancanelli S, Falzetta A, et al. Triple-negative breast cancer: current state of the art. Tumori, 2010, 96: 875-888.
  • 4Pal SK, Childs BH, Pegram M. Triple negative breast cancer: unmet medical needs. Breast Cancer Res Treat, 2011, 125: 627-636.
  • 5Koch A, Bergman B, Holmberg E, et al. Effect of celecoxib on sut~'ival in patients with advanced non-small cell lung cancer: A double blind randomised clinical phase m trial (CYCLUS study) by the Swedish Lung Cancer Study Group. Eur J Cancer, 2011, 47: 1546-1555.
  • 6Du H, Li W, Wang Y, et al. Celeeoxib induces cell apoptosis coupled with up-regulation of the expression of VEGF by a mechanism involving ER stress in human colorectal cancer cells. Oncol Rep, 2011, 26:495-502.
  • 7Gordon JW, Shaw JA, Kirshenbaum LA. Multiple facets of NF- K B in the heart: to be or not to NF- K B. Circ Res, 2011,108:1122-1132.
  • 8Staudt LM. Oncogenic activation of NF-kappaB. Cold Spring Harb Perspect Biol, 2010, 2: a000109.
  • 9Singh S, Shi Q, Bailey ST, et al. Nuclear factor-kappaB activation: a molecular therapeutic target for estrogen receptor-negative and epidermal growth factor receptor family receptor-positive human breast cancer. Mol Cancer Ther, 2007, 6: 1973-1982.
  • 10Valovka T, Hottiger MO. p65 controls NF- K B activity by regulating cellular localization of I K B 13. Biochem J, 2011,434: 253-263.

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