期刊文献+

凋亡及凋亡相关蛋白Bax在局部晚期宫颈癌同步放化疗中的表达 被引量:2

Apoptosis and Expression of Apoptosis-associated Bax Protein during Synchronal Radiochemotherapy of Locally Advanced Uterine Cervix Cancer
下载PDF
导出
摘要 目的:研究局部晚期宫颈鳞癌细胞对同步放化疗应答的分子机制,探讨凋亡及Bax、Bcl-2的表达。方法:49例局部晚期宫颈鳞癌患者随机分为两组:单纯放疗(RT)组25例接受盆腔外照射和后装治疗;同步放化疗(CRT)组24例除接受放疗外,还接受3个周期的化疗(DDP+5-FU)。在治疗前和治疗过程中(RT组:放疗10Gy后;CRT组:放疗10Gy+(DDP+5-FU)×1个周期)分别活检留取标本,用TUNEL法及免疫组化检测凋亡及Bax、Bcl-2的表达。结果:RT组和CRT组完全缓解率分别为52.0%和79.2.0%(P=0.044)。在治疗前和治疗过程中,RT组和CRT组凋亡阳性率均增加,分别由24%上升到60.0%(P=0.01)和20.8%增加到87.5%(P=0.000),差异显著;治疗中CRT组较RT组增加更加明显(P=0.03)。Bax的表达亦增加,分别由24.0%上升到52.0%(P=0.021)和25.0%增加到79.2%(P=0.000),差异显著;CRT组较RT组增加的更显著(P=0.044)。两组在治疗中,凋亡的阳性率和Bax的阳性表达密切相关,CRT组较RT组相关性更强(P=0.015,r=0.827:P=0.027,r=0.523),但两组Bcl-2的表达无变化(P>0.05)。结论:局部晚期宫颈鳞癌,CRT比RT有更好的缓解率,其机制可能是化疗和放疗有协同作用,通过上调Bax通路诱导了肿瘤细胞的凋亡。 Objective: To investigate the molecular mechanism of cell death after radiotherapy or radiochemotherapy of locally advanced uterine eervix cancer (UCC) and to discuss the apoptosis and expression of Bax and Bcl-2 protein. Methods: Forty-nine patients with UCC were randomized into two groups: the radiotherapy (RT) group with 25 patients who were given simple external irradiation of the pelvic cavity and after-loading therapy and, the synehronal radiochemotherapy (CRT) group wilh 24 paliethe nts who were given 3 cycles of chemotherapy (DDP+5-FU) besides RT. Biopsy of the UCC was conducted before and during the treatment (group RT: after 10 Gy radiotherapy: group CRT: 10 Gv radiotherapy+(DDP+5-FU)×1 cycle). The samples obtained in the treatment were employed Io determine apoptosis and the expression of Bax and Bcl-2 protein using TUNEL and immunohistochemical methods. Results: A complete response achieved 52% of the RT group and 79.2%ofCRT group, respectively (P=0.044). Before and during the treatment, the positive rates of apoptosis were increased, ranging from 24% to 60%(P=0.01) in the RT group and from 20.8% to 87.5% (P=0.000) in the CRT group, respectively. There was a significant difference between the two groups, especially during the treatment (P=0.03). The positive rate of Bax protein was increased, too. They were 24% and 25%, before treatment, and 52% and 79.2%, after treatment, in the RT and CRT group, respectively, with a significant difference(P=0.021 and P=0.000). There was a significant correlation between the expression of Bax and apoptosis, after treatment in both groups (P=0.015,r=0.827 vs P=0.027,r=0.523). However, there was no change in the expression of Bcl-2 in the two groups (P〉0.05). Conclusions: There is a better remission rate in CRT of the UCC compared to the RT. An additive or synergistic anti-cancer effect might be the mechanism of CRT, which is realized by up-regulating Bax pathway for induction of tumor-cell ap
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2007年第5期251-254,257,共5页 Chinese Journal of Clinical Oncology
基金 广西壮族自治区卫生厅科研基金资助(编号:Z2005023)
关键词 局部晚期宫颈癌 放疗 放化疗 凋亡 Bax Bcl-2 Locally advanced uterine cervix cancer Radiotherapy Chemoradiotherapy Apoptosis Bax and Bcl-2
  • 相关文献

参考文献10

  • 1Trmble T. Global strategies for cervical cancer control in the 21st cenmry[j]. Gynecol Oncol, 2005, 99(3 Suppl 1): S245. 被引量:1
  • 2Rose PG, Bundy BN, Watkins EB, et al. Concurrent cisplatinbased radiotherapy and chemotherapy for locally advanced cervical cancer[j]. N Engl J Med, 1999, 340(15): 1144-1153. 被引量:1
  • 3Eifel PJ, Winter K, Morris M, et al. Pelvic irradiation with concurrent chemotherapy versus pelvic and para --aortic irradiation for high-risk cervical cancer: an update of radiation therapy oncology group trial (RTOG) 90-01 [j]. J Clin Oncol, 2004, 22(5): 872-880. 被引量:1
  • 4章文华,吴令英.关于子宫颈癌综合治疗的商榷[J].中华肿瘤杂志,2003,25(2):206-208. 被引量:57
  • 5Ararat WO, Gomez-Navarro j, Xiang J, et al. An adenovirus encoding proapoptotic Bax induces apoptosis and enhances the radiation effect in human ovarian cancer[J]. Mol Ther, 2000, 1 (6): 545 -554. 被引量:1
  • 6Guo B, Cao S, Toth K, et al. Overexpression of Bax anhances antitumor activity of chemotherapeutic agents ha human head and neck squamous cell carchloma [J]. Clin Cancer Res,2000, 6 (2): 718-724. 被引量:1
  • 7Lowe SW, Schmitt EM, Smith SW, et al. p53 is required for radiation-induced apoptosis in mouse thymocytes [j]. Nature, 1993, 362(6423): 847-849. 被引量:1
  • 8柳友清,邢辉,韩晓兵,石小艳,梁缝奇,陈刚,马丁.顺铂诱导宫颈癌Hela细胞凋亡及其作用机制的研究[J].中国肿瘤临床,2006,33(1):1-4. 被引量:26
  • 9Xu ZW, Friess H, Buchler MW, et al. Overexpression of Bax sensitizes human pancreatic cancer cells to apoptosis induced by chemotherapeutic agents [j]. Cancer Chemother Pharmacol, 2002, 49(6): 504-510. 被引量:1
  • 10Sultana H, Kigawa J, Kanamori Y, et al. Chemosensifivity and p53-Bax pathway-mediated apoptosis in patients with uterine cervical cancer[j]. Ann Oncol, 2003, 14(2): 214-219. 被引量:1

二级参考文献22

  • 1谭道彩.子宫颈癌Ⅲb期化疗加镭疗的十年疗效[A]..见:第4次全国宫颈癌学术交流会论文摘要汇编[C].,1990.17-18. 被引量:1
  • 2Goff BA, Muntz HG, Paley PJ, et al. Impact of surgical staging in women with locally advanced cervical cancer. Gynecol Oncol, 1999,74:436-442. 被引量:1
  • 3Sedlis A, Bundy BN, Rotman MZ, et al. A randomized trial of pelvic radiation therapy versus no further therapy in selected patients with stage Ⅰb carcinoma of the cervix after radical hysterectomy and pelvic lymphadenectomy: a gynecologic oncology group study. Gynecol Oncol,1999,73:177-183. 被引量:1
  • 4Sardi JE, Girroli A, Sananes C, et al. Long-term follow up of the first randomized trial using neoadjuvant chemotherapy in stage Ⅰ b squamous carcinoma of the cervix: the final results. Gynecol Oncol, 1997,67:61-69. 被引量:1
  • 5Lin JC, Ho ES, Jan JS, et al. High complete response rate of concomitant chemoradiotherapy for locally advanced squamous cell carcinoma of the uterine cervix. Gynecol Oncol, 1996,61:101-108. 被引量:1
  • 6Sugiyama T, Nishida T, Hasuo Y, et al. Neoadjuvant intraarterial chemotherapy followed by radical hysterectomy and /or radiotherapy for locally advanced cervical cancer. Gynecol Oncol, 1998,69:130-136. 被引量:1
  • 7Lahousen M, Haas J, Pickel H, et al. Chemotherapy versus radiotherapy versus observation for high-risk cervical carcinoma after radical hysterectomy: a randomized, prospective, multicenter trial. Gynecol Oncology, 1999, 73: 196-201. 被引量:1
  • 8Tattersall MH, Ramirez C, Coppleson M. A randomized trial of adjuvant chemotherapy after radical hysterectomy in stage Ⅰb-Ⅱa cervical cancer carcinoma of patients with pelvic lymph node metastases. Gynecol Oncol,1992,46:176-181. 被引量:1
  • 9Thomas G, Dembo A, Ackerman I, et al. A randomized trial of standard versus partially hyperfractionated radiation with or without concurrent 5-fluorouracil in locally advanced cervical cancer. Gynecol Oncol, 1998,69:137-145. 被引量:1
  • 10Panici PB, Scambia G, Baiocchi G, et al. Neoadjuvant chemotherapy and radical surgery in locally advanced cervical cancer: prognostic factors for response and survival. Cancer, 1991,67:372-379. 被引量:1

共引文献81

同被引文献18

  • 1Monika Olempska,Patricia Alice Eisenach,Ole Ammerpohl,Hendrik Ungefroren,Fred Fandrich,Holger Kalthoff.Detection of tumor stem cell markers in pancreatic carcinoma cell lines[J].Hepatobiliary & Pancreatic Diseases International,2007,6(1):92-97. 被引量:69
  • 2Zhang L, Yang X, Pan HY, Zhou XJ, Li J, Chen WT, Zhong LP, Zhang ZY. Expression of growth dif- ferentiation factor 15 is positively correlated with histopathological malignant grade and in vitro cell proliferation in oral squamous cell carcinoma. Oral Oncol 2009; 45:627-632 [PMID: 18805046 DOI: 10.1016/j.oraloncology.2008.07.017]. 被引量:1
  • 3Baek SJ, Kim KS, Nixon JB, Wilson LC, Eling TE. Cyclooxygenase inhibitors regulate the expression of a TGF-beta superfamily member that has pro-apoptotic and antitumorigenic activities. Mol Phar- macol 2001; 59:901-908 [PMID: 11259636]. 被引量:1
  • 4Albertoni M, Shaw PH, Nozaki M, Godard S, Tenan M, Hamou MF, Faiflie DW, Breit SN, Paralkar VM, de Tribolet N, Van Meir EG, Hegi ME. Anoxia in- duces macrophage inhibitory cytokine-1 (MIC-1) in glioblastoma cells independently of p53 and HIF-1. Oncogene 2002; 21:4212-4219 [PMID: 12082608]. 被引量:1
  • 5Johnen H, Lin S, Kuffner T, Brown DA, Tsai VW, Bauskin AR, Wu L, Pankhurst G, Jiang L, Junankar S, Hunter M, Fairlie WD, Lee NJ, Enriquez RF, Baldock PA, Corey E, Apple FS, Murakami MM, Lin EJ, Wang C, During MJ, Sainsbury A, Herzog H, Breit SN. Tu- mor-induced anorexia and weight loss are mediated by the TGF-beta superfamily cytokine MIC-1. Nat Med 2007; 13:1333-1340 [PMID: 17982462]. 被引量:1
  • 6Kim KK, Lee JJ, Yang Y, You KH; Lee JH. Macro- phage inhibitory cytokine-1 activates AKT and ERK-1/2 via the transactivation of ErbB2 in human breast and gastric cancer cells. Carcinogenesis 2008; 29:704-712 [PMID: 18258606 DOh 10.1093/carcin/ bgn031]. 被引量:1
  • 7Boyle GM, Pedley J, Martyn AC, Banducci KJ, Strutton GM, Brown DA, Breit SN, Parsons PG. Macrophage inhibitory cytokine-1 is overexpressed in malignant melanoma and is associated with tumorigenicity. J Invest Dermatol 2009; 129:383-391 [PMID: 18754039 DOI: 10.1038/]id.2008.270]. 被引量:1
  • 8Senapati S, Rachagani S, Chaudhary K, Johansson SL, Singh RK, Batra SK. Overexpression of macro- phage inhibitory cytokine-1 induces metastasis of human prostate cancer cells through the FAK-RhoA signaling pathway. Oncogene 2010; 29:1293-1302 [PMID: 19946339 DOh 10.1038/onc.2009.420]. 被引量:1
  • 9Lee DH, Yang Y, Lee SJ, Kim KY, Koo TH, Shin SM, Song KS, Lee YH, Kim YJ, Lee JJ, Choi I, Lee JH. Macrophage inhibitory cytokine-1 induces the invasiveness of gastric cancer cells by up-regulating the urokinase-type plasminogen activator system. Cancer Res 2003; 63:4648-4655 [PMID: 12907645]. 被引量:1
  • 10Zou XM, Li YL, Wang H, Cui W, Li XL, Fu SB, Jiang HC. Gastric cancer cell lines induced by trichostatin A. World J Gastroenterol 2008; 14:48104815 [PMID: 1872O545]. 被引量:1

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部