期刊文献+

长链非编码RNA MEG3在胚胎性横纹肌肉瘤凋亡中的研究 被引量:6

Apoptotic study of long non-coding RNA MEG3 in embryonal rhabdomyosarcoma
下载PDF
导出
摘要 目的研究人类长链非编码RNA(lncRNAs)母系印记基因3(MEG3)在胚胎性横纹肌肉瘤凋亡中的作用,并探讨其分子机制。方法分析18例胚胎性横纹肌肉瘤的临床特征,免疫组织化学法检测肿瘤组织凋亡相关基因产物的表达,TUNEL法检测凋亡指数,qRT-PCR法检测MEG3在18例胚胎性横纹肌肉瘤及7例正常骨骼肌中的表达情况。结果 18例胚胎性横纹肌肉瘤临床表现因发病部位不同可有多种临床症状,免疫组织化学检测与肿瘤凋亡相关的P53、Caspase-9及Caspase-3均阳性表达,Ki-67核增殖指数达40%;TUNEL法检测平均凋亡指数为37%;qRT-PCR法检测18例胚胎性横纹肌肉瘤组织中MEG3表达较7例正常骨骼肌组织显著增高(P<0.05)。结论 MEG3与胚胎性横纹肌肉瘤凋亡呈正相关关系。 Objective To study the role of human long non-coding RNAs (|ncRNAs) maternally imprinted genes 3 (MEG3) on the apoptosis of embryonal rhabdomyosarcoma (eRMS) as well as its molecular mechanisms. Methods The clinical manifestations, immunohistochemical staining and TUNEL apoptotic experiment were observed in 18 eRMS samples and 7 normal skeletal muscle samples. Real-time quantitative polymerase chain reaction (qRT-PCR) was used to analyze the expression of MEG3. Results Ten males and 8 females aged from 4 months to 6 years ( with an average age of 2. 5 years) were enrolled in this study, eRMS usually showed diverse clinical symptoms according to its anatomic origins, which is generally due to the obstruction of the mass. Immunohistochemistry indicated positive expression of P53, Caspase-9 and Caspase-3. The proliferation index of Ki-67 was more than 40%. Tunel apoptotic assay showed yellow-green fluorescence in tumor cells, qRT-PCR analysis indicated an over expression of MEG3 in eRMS samples (P 〈 0.05 ). Conclusions MEG3 had a positive correlation with the apoptosis in eRMS.
出处 《中国小儿血液与肿瘤杂志》 CAS 2013年第3期120-123,128,共5页 Journal of China Pediatric Blood and Cancer
基金 深圳市科技计划项目(项目编号:201102071) 广东省自然科学基金(项目编号:No.S2011010004349)
关键词 长链非编码RNA 胚胎性横纹肌肉瘤 MEG3 凋亡 Long non-coding RNAs Embryonal rhabdomyosarcoma MEG3 Apoptosis
  • 相关文献

参考文献15

  • 1Mercer TR, Dinger M, Mattick JS. Long non-coding RNAs : insightsinto functions. Nat Kev Genet, 2009, 10: 155-159.
  • 2Wang F, Hen Z, Sun P. Overexpression of the long non-coding RNAMEG3 impairs in vitro giioma cell proliferation. J Cell Biochem,2012, 113:1868-1874.
  • 3Pang KC, Dinger ME, Mercer TR,et al. Genome-wide identification oflong nonctxling HNAs in CDS + T cells. J Immunol, 2009 , 182:7738-7748.
  • 4Cheunsuchon P, Zhou Y, Zhang X, et al. Silencing of the imprintedDLK1-MLG3 locus in human clinically nonfunctioning pituitaryadenomas. Am J Pathol, 2011 , 10,179: 2120-2130.
  • 5Mercer fR, Dinger ME, Sunkin SM,et al. Specific expression oflong noncoding RNAs in the mouse brain. Proc Natl Acad Sci USA,2008,105: 716-721.
  • 6Miyoshi N, Wagatsuma H, Wakana S, et al. Identification of animprinted gene, Meg3/Gtl2 and its human homologue MEG3,firstmapped on mouse distal chromosome 12 and human chromosomeI4q. Genes Cells, 2000, 5: 211-220.
  • 7Balik V,Srovnal J, Sulla I,et al. MEG3 : a novel long noncodingpotentially tumour-suppressing RNA in meningiomas. J Neurooncol,2013,112: 1*8.
  • 8McMurray EN, Schmidt JV. Identification of imprinting regulators atthe Meg3 differentially methylated region. Genomics, 2012,100 :184-94.
  • 9Anwar SL, Krech T, Hasemeier B, et aL Loss of imprinting andallelic switching at the DLK1-MEG3 locus in human hepatocellularcarcinoma. PLoS One, 2012,7: e49462.
  • 10Benetatos L, Voulgaris E, Vartholomatos G. DLK1-MEG3 imprinteddomain microRNAs in cancer biology. Crit Rev Eukaryot Gene Expr,2012,22:1-15.

同被引文献38

  • 1Kung JT, Colognori D, Lee Jr. Long noncodnig RNAs: past, pres- ent, and future [J]. Genetics, 2013, 193(3): 651-669.
  • 2Wang KC, Chang HY. MolecuLar mechanisms of long noncoding RNAs [J]. Mol Cell, 2011, 43(6): 904-914.
  • 3Zhou Y, Zlaang X, Klibanski A. MEG3 noncoding RNA: a tumor suppressor [J-J. J MoI EndoctinoI, 2012, 48(3): R45-53.
  • 4Braconi C, Kogure T, Valeri N, et al. microRNA-29 can regulate ex- pression of the long non-coding RNA gene MEG3 in hepatocelhilar cancer [J]. Oncogene, 2011, 30(47): 4750-4756.
  • 5Hansman DM. How can irregular causal generalizations guide prac- tice? [J]. Prey Med, 2011, 53(4-5): 229-231.
  • 6Li Z, Li C, Liu C, et al. Expression of the long non-coding RNAs MEG3, HOTAIR, and MALAT-I in non-functioning pituitary ade- nomas and their relationship to tumor behavior [J]. Pituitary, 2014, 31: 879.
  • 7Lu KH, Li W, Liu XH, et al. Long non-coding RNA MEG3 inhibits NSCLC cells proliferation and induces apoptosis by affecting p53 expression [J]. BMC Cancer, 2013, 13(1471-2407): 461.
  • 8Russo AL, Ryan DP, Borger DR, et al. Mutational and clinical predictors of pathologic complete response in the treatment of locally advanced rectal cancer [J]. J Gastrointest Cancer, 2014, 45 (1): 34-39.
  • 9Wang P, Ren Z, Sun P. Overexpression of the long non-coding RNA MEG3 impairs in vitro glioma cell proliferation [J]. J Cell Bioqhem, 2012, 113(6): 1868-1874.
  • 10Qin 1L Chen Z, Ding Y, et al. Long non-coding RNA MEG3 inhibits the proliferation of cervical carcinoma ceils through the induction of cell cycle arrest and apoptosis [J]. Neoplasma, 2013, 60(5): 486-492.

引证文献6

二级引证文献10

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