[1]郭艳婷,张鹏飞,刘强.Smac与肿瘤放射治疗[J].国际放射医学核医学杂志,2013,37(5):309-313.[doi:10.3760/cma.j.issn.1673-4114.2013.05.014]
 GUO Yan-ting,ZHANG Peng-fei,LIU Qiang.Effects of Smac on tumor radiotherapy[J].International Journal of Radiation Medicine and Nuclear Medicine,2013,37(5):309-313.[doi:10.3760/cma.j.issn.1673-4114.2013.05.014]
点击复制

Smac与肿瘤放射治疗(/HTML)
分享到:

《国际放射医学核医学杂志》[ISSN:1673-4114/CN:12-1381/R]

卷:
37
期数:
2013年第5期
页码:
309-313
栏目:
综述
出版日期:
2013-09-25

文章信息/Info

Title:
Effects of Smac on tumor radiotherapy
作者:
郭艳婷 张鹏飞 刘强
300192 天津, 北京协和医学院中国医学科学院放射医学研究所, 天津市分子核医学重点实验室
Author(s):
GUO Yan-ting ZHANG Peng-fei LIU Qiang
Tianjin Key Laboratory of Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science, Peking Union Medical College, Tianjin 300192, China
关键词:
细胞凋亡肿瘤Smac半胱氨酸天冬氨酸蛋白酶凋亡抑制蛋白类辐射耐受性
Keywords:
ApoptosisNaoplasmsSmacCaspaseInhibitor of apoptosis proteinsRadiation tolerance
DOI:
10.3760/cma.j.issn.1673-4114.2013.05.014
摘要:
放射治疗是肿瘤治疗的一个重要手段,肿瘤的辐射敏感性与凋亡蛋白抑制家族(IAPs)和促凋亡蛋白第二线粒体来源的Caspase激活因子(Smac)密切相关。IAPs能够通过结合Caspase-3、7、9抑制凋亡,IAPs的高表达是肿瘤细胞出现辐射抵抗的重要机制之一。当细胞接收到凋亡刺激信号后,Smac即从线粒体释放至胞质内与IAPs结合从而释放Caspase,发挥其促凋亡活性。以IAPs为靶点的治疗可能会为肿瘤细胞克服放射抵抗打开新的视角。临床前的体内体外研究证明,这种联合治疗值得更进一步的临床研究。使用IAPs拮抗剂联合放射治疗可能会为更有效的放射治疗肿瘤患者铺平道路。
Abstract:
Radiotherapy is one of the main methods of tumor therapy.The radiosensitivity of tumor is closely related to inhibitor of apoptosis proteins (IAPs)and the second mitochondria-derived activator of Caspase (Smac).IAPs can inhibit apoptosis by binding and inhibiting Caspase-3, 7, 9.High expression of IAPs has been shown to interfere with the efficacy of radiotherapy.Smac, upon apoptotic stimuli, is released into the cytoplasm to inhibit the caspase-binding activity of IAPs.Therapies targeting of IAP proteins may show new perspectives to overcome radioresistance.In vitro and in vivo precIinical studies have demonstrated that the combination approach warranted further clinical investigation.Thus, combination protocols using IAPs antagonists together with radiotherapy may pave the avenue to more effective radiation-based treatment options for tumor patients.

参考文献/References:

[1] Spencer SL, Sorger PK. Measuring and modeling apoptosis in single cells. Cell, 2011, 144(6):926-939.
[2] O’Brien MA, Kirby R. Apoptosis:A review of pro-apoptotic and anti-apoptotic pathways and dysregulation in disease[DB/OL].WILEY:J Vet Emerg Crit Care, 2008[2013-03-14]. http://onli-nelibrary.wiley.com/doi/10.1111/j.1476-4431.2008.00363.x/full.
[3] Greer RM, Peyton M, Larsen JE, et al. SMAC Mimetic (JP1201) sensitizes non-small cell lung cancers to multiple chemotherapy agents in an IAP-dependent but TNF-a-independent manner. Can-cer Res, 2011,71(24):7640-7648.
[4] Olsson M, Zhivotovsky B. Caspases and cancer. Cell Death Differ,2011,18(9):1441-1449.
[5] Hartman ML, Czyz M. Anti-apoptotic proteins on guard of melanoma cell survival. Cancer Lett, 2013,331(1):24-34.
[6] Qin S, Yang C, Li S, et al. Smac:Its role in apoptosis induction and use in lung cancer diagnosis and treatment. Cancer Lett, 2012,318(1):9-13.
[7] Du C, Fang M, Li Y, et al. Smac, a mitochondrial protein that pro-motes cytochrome c-dependent caspase activation by eliminating IAP inhibition. Cell, 2000, 102(1):33-42.
[8] Verhagen AM, Ekert PG, Pakusch M, et al. Identification of DIA-BLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins. Cell, 2000,102(1):43-53.
[9] Huang Y, Park YC, Rich RL, et al. Structural basis of caspase inhibition by XIAP:differential roles of the linker versus the BIR domain. Cell, 2001, 104(5):781-790.
[10] Riedl SJ, Renatus M, Schwarzenbacher R, et al. Structural basis for the inhibition of caspase-3 by XIAP. Cell, 2001, 104(5):791-800.
[11] Bao ST, Gui SQ, Lin MS. Relationship between expression of Smacand Survivin and apoptosis of primary hepatocellular carcinoma.Hepatobiliary Pancreat Dis Int, 2006, 5(4):580-583.
[12] Kempkensteffen C, Jager T, Bub J, et al. The equilibrium of XIAP and Smac/DIABLO expression is gradually deranged during the development and progression of testicular germ cell tumours. Int J Androl, 2007, 30(5):476-483.
[13] Kempkensteffen C, Hinz S, Christoph F, et al. Expression levels of the mitochondrial IAP antagonists Smac/DIABLO and Omi/HtrA2 in clear-cell renal cell carcinomas and their prognostic value. J Cancer Res Clin Oncol, 2008, 134(5):543-550.
[14] Martinez-Ruiz G, Maldonado V,Ceballos-Cancino G, et al. Role of Smac/DIABLO in cancer progression. J Exper Clin Cancer Res,2008,27(1):48.
[15] Pluta P, Cebula-Obrzut B, Ehemann V, et al. Correlation of Smac/DIABLO protein expression with the clinico-pathological features of breast cancer patients. Neoplasma, 2011, 58(5):430-435.
[16] Sekimura A, Konishi A, Mizuno K, et al. Expression of Smac/DIA-BLO is a novel prognostic marker in lung cancer. Oncol Rep, 2004,11(4):797-802.
[17] 陈晓,杨春鹿,赵君,等.非小细胞肺癌组织Livin和Smac蛋白表达及其临床意义的研究.中华肿瘤防治杂志,2008(12):144-149.
[18] Dai CH, Li J, Shi SB, et al. Survivin and Smac gene expressions but not livin are predictors of prognosis in non-small cell lung cancer patients treated with adjuvant chemotherapy following surgery. Jpn JClin Oncol, 2010, 40(4):327-335.
[19] 杨莉晖,单春光,黄红梅,等.Smac和survivin在鼻腔鼻窦内翻性乳头状瘤中的表达.临床耳鼻咽喉头颈外科杂志,2013,27(8):407-410.
[20] McNeish IA, Bell S, McKay T, et al. Expression of Smac/DIABLO in ovarian carcinoma cells induces apoptosis via a caspase-9-medi-ated pathway. Exper Cell Res, 2003, 286(2):186-198.
[21] Giagkousiklidis S, Vogler M, Westhoff MA, et, al. Sensitization for gamma-irradiation-induced apoptosis by second mitochondria-derived activator of caspase. Cancer Res, 2005, 65(22):10502-10513.
[22] Fandy TE, Shankar S, Srivastava RK. Smac/DIABLO enhances the therapeutic potential of chemotherapeutic drugs and irradiation,and sensitizes TRAIL-resistant breast cancer cells. Mol Cancer,2008,7(1):60.
[23] Chen DJ, Huerta S. Smac mimetics as new cancer therapeutics.Anticancer Drugs, 2009, 20(8):646-658.
[24] Berger R, Jennewein C, Marschall V, et al. NF-kB is required for Smac mimetic-mediated sensitization of glioblastoma cells for y-irradiation-induced apoptosis. Mol Cancer Ther, 2011, 10(10):1867-1875.
[25] Li W, Li B, Giacalone NJ, et al. BV6, an IAP antagonist, activates apoptosis and enhances radiosensitization of non-small cell lung carcinoma in vitro. J Thoracic Oncol, 2011, 6(11):1801-1809.
[26] Ziegler DS, Keating J, Kesari S,et al. A small-molecule IAP inhibitor overcomes resistance to cytotoxic therapies in malignant gliomas in vitro and in vivo. Neuro Oncology, 2011, 13(8):820-829.
[27] Yang D, Zhao Y, Li A Y, et al. Smac-mimetic compound SM-164 induces radiosensitization in breast cancer cells through activation of caspases and induction of apoptosis. Breast Cancer Res Treat,2012, 133(1):189-199.
[28] Zhang S, Li G,Zhao Y, et al. Smac mimetic SM-164 potentiates AP02L/TRAIL-and doxorubicin-mediated anticancer activity in human hepatocellular carcinoma cells[J/OL]. San Francisco:PLoS One, 2012[2013-03-14]. http://www.ncbi.nlm.nih.gov/pubmed/23240027.
[29] Dai Y, Liu M, Tang W, et al. Molecularly targeted radiosensitization of human prostate cancer by modulating inhibitor of apoptosis. Clin Cancer Res, 2008, 14(23):7701-7710.
[30] Huerta S, Gao X, Livingston EH, et al. In vitro and in vivo radiosensitization of colorectal cancer HT-29 cells by the smac mimetic JP-1201. Surgery, 2010, 148(2):346-353.
[31] Chen F, Xu C, Du L, et al. Tat-SmacN7 induces radiosensitization in cancer cells through the activation of caspases and induction of apoptosis. Int J Oncol, 2013, 42(3):985.

相似文献/References:

[1]何燕,苏晋,郑晓霞,等.P-糖蛋白抑制剂在PET显像中的应用研究[J].国际放射医学核医学杂志,2016,40(1):1.[doi:10.3760/cma.j.issn.1673-4114.2016.01.001]
 He Yan,Su Jin,ZhengXiaoxia,et al.Developing P-glycoprotein inhibitor marked by PET[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):1.[doi:10.3760/cma.j.issn.1673-4114.2016.01.001]
[2]许飞,刘建军,黄钢,等.PET乏氧显像在预测肿瘤乏氧及指导临床治疗中的应用进展[J].国际放射医学核医学杂志,2016,40(1):35.[doi:10.3760/cma.j.issn.1673-4114.2016.01.008]
 Xu Fei,Liu Jianjun,Huang Gang,et al.The application of hypoxia imaging with PET in predicting tumor hypoxia and guiding clinical therapy[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):35.[doi:10.3760/cma.j.issn.1673-4114.2016.01.008]
[3]陈晓艳,张江虹,邵春林.STAT3与辐射敏感相关性的研究进展[J].国际放射医学核医学杂志,2016,40(3):191.[doi:10.3760/cma.j.issn.1673-4114.2016.03.007]
 Chen Xiaoyan,Jianghong,Shao Chunlin.Research progresses of correlation between STAT3 and radiosensitivity[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):191.[doi:10.3760/cma.j.issn.1673-4114.2016.03.007]
[4]张俊伶,薛晓蕾,李源,等.富氢水对电离辐射引起胸腺细胞损伤的影响[J].国际放射医学核医学杂志,2015,39(5):358.[doi:10. 3760 / cma. j. issn. 1673-4114. 2015. 05. 001]
 zhang junling,xue xiaolei,li yuan,et al.effects of hydrogen-rich water on radiation-induced thymus injury[J].International Journal of Radiation Medicine and Nuclear Medicine,2015,39(5):358.[doi:10. 3760 / cma. j. issn. 1673-4114. 2015. 05. 001]
[5]赵舒怡,储小飞,樊赛军.血清肿瘤标志物与肿瘤放疗疗效评估的研究进展[J].国际放射医学核医学杂志,2015,39(5):427.[doi:10. 3760 / cma. j. issn. 1673-4114. 2015. 05. 018]
 zhao shuyi,chu xiaofei,fan saijun..progression of study on serum tumor markers in evaluation of tumor radiotherapy[J].International Journal of Radiation Medicine and Nuclear Medicine,2015,39(5):427.[doi:10. 3760 / cma. j. issn. 1673-4114. 2015. 05. 018]
[6]赵徵鑫,翟贺争,张文艺,等.质子重离子治疗肿瘤的进展[J].国际放射医学核医学杂志,2016,40(5):384.[doi:10.3760/cma.j.issn.1673-4114.2016.05.010]
 Zhao Zhixin,Zhai Hezheng,Zhang Wenyi,et al.Development of proton heavy ion in tumor therapy[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):384.[doi:10.3760/cma.j.issn.1673-4114.2016.05.010]
[7]任佳忠,李永梅,刘岩,等.99Tcm-MDP骨显像胸部异常放射性摄取的原因分析[J].国际放射医学核医学杂志,2016,40(6):459.[doi:10.3760/cma.j.issn.1673-4114.2016.06.011]
 Jiazhong,Li Yongmei,Liu Yan,et al.Reasons for the abnormal 99Tcm-MDP uptake in the thoracic tissue on bone scintigraphy[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):459.[doi:10.3760/cma.j.issn.1673-4114.2016.06.011]
[8]马彦云,张辉.磁共振体素内不相干运动扩散加权成像的原理及应用进展[J].国际放射医学核医学杂志,2016,40(6):469.[doi:10.3760/cma.j.issn.1673-4114.2016.06.013]
 Ma Yanyun,Zhang Hui.The basic principle and application progress of intravoxel incoherent motion imaging[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):469.[doi:10.3760/cma.j.issn.1673-4114.2016.06.013]
[9]安淑娴,宋少莉,黄钢.放射性核素标记的凋亡显像剂的研究进展[J].国际放射医学核医学杂志,2015,39(6):470.[doi:10.3760/cma.j.issn.1673-4114.2015.06.008]
 An Shuxian,Song Shaoli,Huang Gang.Recent advances in apoptosis imaging using radionuclide-labeled tracers[J].International Journal of Radiation Medicine and Nuclear Medicine,2015,39(5):470.[doi:10.3760/cma.j.issn.1673-4114.2015.06.008]
[10]杨卫东,汪静.肿瘤核素靶向治疗新进展[J].国际放射医学核医学杂志,2015,39(1):19.[doi:10.3760/cma.j.issn.1673-4114.2015.01.006]
 Yang Weidong,Wang Jing.Advance progress of radionuclide target tumor therapy[J].International Journal of Radiation Medicine and Nuclear Medicine,2015,39(5):19.[doi:10.3760/cma.j.issn.1673-4114.2015.01.006]
[11]陈顺军,程兵.肿瘤细胞凋亡核素显像分子探针研究进展[J].国际放射医学核医学杂志,2016,40(2):149.[doi:10.3760/cma.j.issn.1673-4114.2016.02.013]
 Chen Shunjun,Cheng Bing.Progress in molecular probes of radionuclide tumor apoptosis imaging[J].International Journal of Radiation Medicine and Nuclear Medicine,2016,40(5):149.[doi:10.3760/cma.j.issn.1673-4114.2016.02.013]
[12]张敬勉,赵新明,王建方,等.99Tc-亚甲基二膦酸盐与153Sm-乙二胺四亚甲基膦酸对骨侵袭和骨质溶解抑制作用的对比研究[J].国际放射医学核医学杂志,2008,32(6):321.
 ZHANG Jing-mian,ZHAO Xin-ming,WANG Jian-fang,et al.The comparative study of inhibitory effects of 99Tc-methylenediphosphonate and 153Sm-ethylene diamine tetramethylene phosphonic acid on bone invasion and osteolysis[J].International Journal of Radiation Medicine and Nuclear Medicine,2008,32(5):321.
[13]张欣,李亚明.99mTc标记annexin V类显像剂细胞凋亡显像在肿瘤研究中的应用及进展[J].国际放射医学核医学杂志,2006,30(4):210.
 ZHANG Xin,LI Ya-ming.Application and advance of apoptosis 99mTc labelled annexin V imaging in tumor research[J].International Journal of Radiation Medicine and Nuclear Medicine,2006,30(5):210.
[14]黄代娟.放射性核素标记annexin V凋亡显像在肿瘤研究中的进展[J].国际放射医学核医学杂志,2003,27(4):165.
 HUANG Dai-juan.Advance of apoptosis imaging with radiolabeled annexin V in tumor research[J].International Journal of Radiation Medicine and Nuclear Medicine,2003,27(5):165.
[15]林亚华,叶巧滔.FHIT基因研究进展[J].国际放射医学核医学杂志,2001,25(6):275.
 LIN Ya-hua,YE Qiao-tao.Advances of FHIT gene[J].International Journal of Radiation Medicine and Nuclear Medicine,2001,25(5):275.
[16]元龚骏,聂大红,唐刚华.临床用肿瘤细胞凋亡核医学显像剂研究进展[J].国际放射医学核医学杂志,2017,41(4):271.[doi:10.3760/cma.j.issn.1673-4114.2017.04.007]
 Yuan Gongjun,Nie Dahong,Tang Ganghua.Progress of nuclear medicine imaging agents for the clinical apoptosis imaging of tumors[J].International Journal of Radiation Medicine and Nuclear Medicine,2017,41(5):271.[doi:10.3760/cma.j.issn.1673-4114.2017.04.007]
[17]刘成,程竞仪,章英剑.碳离子射线诱导细胞凋亡的研究进展[J].国际放射医学核医学杂志,2018,(1):58.[doi:10.3760/cma.j.issn.1673-4114.2018.01.011]
 Liu Cheng,Cheng Jingyi,Zhang Yingjian.Progress in cell apoptosis induced by carbon ion beam[J].International Journal of Radiation Medicine and Nuclear Medicine,2018,(5):58.[doi:10.3760/cma.j.issn.1673-4114.2018.01.011]

备注/Memo

备注/Memo:
收稿日期:2013-03-15。
基金项目:国家自然科学基金(31200634,31170804,31240052);天津市自然科学基金(12JCYBJC15300,13JCYBJC23500)
通讯作者:刘强,Email:liuqiang@irm-cams.ac.cn
更新日期/Last Update: 1900-01-01