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端粒酶逆转录酶反义寡核苷酸对甲状腺癌细胞凋亡的影响

Effect of antisense oligonucleotides encoding telomerase reverse transcriptase on thyroid carcinoma cell apoptosis
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摘要 目的:探讨端粒酶逆转录酶(TERT)的反义寡核苷酸(ASODN)对甲状腺癌(TC)细胞凋亡的影响.方法:体外培养TC细胞,TERTASODN和正义寡核苷酸(SODN)分别作用于体外培养的TC细胞,采用透射电镜,Hoechest荧光染色,流式细胞仪等方法分析ASODNTERT对TC细胞凋亡的影响.结果:透射电镜示ASODN可诱导TC出现典型的细胞凋亡形态,Hoechest荧光染色显示ASODN可使TC凋亡数目增多从52±16上升到178±32,流式细胞仪证实5μmol/LASODN处理组,SODN处理组及空白对照组的细胞凋亡率分别为10.4%,1.6%和无凋亡(P<0.05).结论:TERTASODN能增强TC细胞凋亡. AIM: To investigate the effect of antisense oligonu- cleotides (ASODN) encoding telomerase reverse transcriptase (TERT) mRNA on thyroid carcinoma (TC) cell apoptosis. METHODS: The ASODN and sense oligonucleotides (SODN) encoding TERT were delivered respectively to the TC cells in vitro. The effect of ASODN encoding TERT mRNA on TC cell apoptosis was detected by transmission electron microscope, Hoechest 33258 staining and flow cytometry. RESULTS: Transmission electron microscope showed ASODN could induce typical apoptotic manifestations of TC cells; Hoechest 33258 staining showed ASODN could increase the number of apoptotic cells from 52 ± 16 to 178 ± 32; flow cytometry revealed that the apoptosis rates of TC cells treated by 5 umol/L ASODN, SODN, or nothing were 10.4% , 1.6% and 0, respectively ( P 〈 0. 05 ). CONCLUSION: ASODN complementary to TERT mRNA at some concentration can sequence-specifically enhance TC cell apoptosis.
出处 《第四军医大学学报》 北大核心 2007年第7期624-626,共3页 Journal of the Fourth Military Medical University
关键词 甲状腺肿瘤 寡核苷酸类 反义 端粒酶逆转录酶 thyroid neoplasms oligonucleotides, antisense telomerase reverse transcriptase
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  • 1Dahsc R, Ficdler W, Error G. Telomeres and telomerase: biological and clinical importance. Clin Chem 1997; 43:708-714.
  • 2Yan P,Coindre JM,Benhattar J,Bosman FT,Guillou L.Telomerase activity and human telomerase reverse transcriptase mRNA exprsssion in soft tissue tumors: correlation with grade, histology,and proliferative activity. Cancer Res 1999; 59:3166-3170.
  • 3Feng J, Funk WD, wang SS, Weinrich SL, Avilion AA, Chiu CP,Adams RR, Chang E, Allsopp RC, Yu J. The RNA component ofhuman telomerase. Science 1995: 269:1236-1241.
  • 4Norton JC, Piatyszek MA, Wright WE, Shay JW, Corey DR. Inhibition of human telomerase activity by peptide nucleic acids. Nat Biotechnol 1996; 14:615-619.
  • 5Harrington L, Mcphail T, Mar V, Zhou W, Oulton R, Bass MB,Arruda I, Robinson MO. A mammalian telomerase-associated protein. Science 1997: 275:97.~,-977.
  • 6Nakayama J, Saito M, Nakamura H, Matsuura A, Ishikawa F.TLPI: a gene encoding a protein component of mammali telomerase is a novel member of WD repeats family. Cell 1977; 88:875-884.
  • 7Nakamura TM,Morin GB,Chapman KB,Weinrich SL,Andrews WH, Lingner J, Harley CB, Cech TR. Telomerase catalytic subunit homologs from fission yeast and humarL Science 1997; 277:955-959.
  • 8Meyerson M, Counter CM, Eaton EN, Ellisen LW, Steiner P,Caddle SD, Ziaugra L, Beijersbergen RL, Davidoff MJ, Liu Q,Bacchetti S, Haber DA, Weinberg RA. hEST2, the putative human telomerase catalytic subun gene, is up-regulated in tumor cells and during immortalization. Cell 1997; 90:785-795.
  • 9Kilian A, Bowtell DD, Abud HE, Hime GR, Venter DJ, Keese PK Duncan EL, Reddel RR, Jefferson RA. Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing pattern in different cell types. Hum Mol Genet 1997;6:2011-2019.
  • 10Blasco MA, Funk W, Villeponteau B, Greider CW. Functional characterization and developmental regulation of mouse telomerase RNA. Science 1995; 269:1267-1270.

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