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结肠癌组织中肺腺癌转移相关转录本1的表达及其临床意义 被引量:3

Expression of long non-coding RNAs metastasis associated lung adenocarcinoma transcript 1 in colorectal cancer and its clinical significance
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摘要 目的探讨长链非编码RNA肺腺癌转移相关转录本1(MALAT1)在结肠癌组织中的表达及其临床意义。方法收集121例结肠腺癌组织标本,并以其自身正常组织作为对照,提取组织RNA,实时定量聚合酶链反应法检测结肠癌及其自身正常对照组织中MALAT1的表达水平,并在结肠癌细胞系SW620中过表达MALAT1,观察其对肿瘤细胞迁移的影响。结果结肠癌组织MALAT1表达较自身正常对照组织表达显著升高(P<0.01)。有淋巴结转移的结肠癌组织中MALAT1的表达高于无淋巴结转移的结肠癌组织(P<0.05);有淋巴结转移的结肠癌标本中,淋巴结组织中MALAT1的相对表达量高于结肠癌组织(P<0.05)。SW620转染pc DNA3/MALAT1基因组迁移细胞数明显高于单纯SW620细胞组和SW620转染载体pc DNA3组(P<0.05);单纯SW620细胞组与SW620转染载体pc DNA3组迁移细胞数比较差异无统计学意义(P>0.05)。结论在结肠癌中,长链非编码RNA-MALAT1可作为一个潜在的检测指标,为临床判定预后和后期治疗提供理论基础。 Objective To investigate the expression of long non-cording RNA metastasis associated lung adenocarcinoma transcript 1( MALAT1) in colorectal cancer( CRC) and its clinical significance. Methods Case-matched tissues of CRC tissue and adjacent normal tissue( n = 121) were selected. Quantitative polymerase chain reaction was carried out to examine the expression of MALAT1 in CRC tissue and adjacent normal tissue. The MALAT1 was over-expression in SW620 cell line in order to observe its effect on the tumor cell migration. Results The expression of MALAT1 in CRC tissue was significantly higher than that in adjacent normal tissue( P 0. 01). The expression of MALAT1 in CRC tissue of the patients who had lymphatic metastasis was significantly higher than that of the non-lymphatic metastasis patients( P 0. 05). Similarly,in the CRC metastasis patients,there was a higher expression of MALAT1 in the nodes than that in the original tumor tissues( P 0. 05).The number of metastasis SW620 cells was higher in the pc DNA3 / MALAT1 gene group compared with SW620 group and pc DNA3-SW620 group( P 0. 05). While the number of metastasis SW620 cells had no significant difference between SW620 group and pc DNA3-SW620 group( P 0. 05). Conclusion The expression of MALAT1 has the potential to serve as a diagnostic indicator,it can provide the rationale for judging prognosis and later stage treatment of CRC.
出处 《新乡医学院学报》 CAS 2015年第4期329-331,共3页 Journal of Xinxiang Medical University
关键词 长链非编码RNA 肺腺癌转移相关转录本1 结肠癌 long non-cording RNA metastasis associated lung adenocarcinoma transcript 1 colorectal cancer
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参考文献13

  • 1肖颖,王正晖,牛秀珑,申去非.RNA干扰INK4位点反义非编码RNA抑制人肺癌细胞系生长的分子机制[J].新乡医学院学报,2013,30(4):259-261. 被引量:4
  • 2Gontan C, Jonkers I, Gribnau J. Long noneoding RNAs and X chro- mosome inactivation[ J]. Prog Mol Subcell Bio1,2011,51:43-64. 被引量:1
  • 3Autuoro J M, Pirnie S P, Carmiehael G G. Long noncoding RNAs in imprinting and X chromosome inactivation [ J ]. Biomolecules, 2014,4( 1 ) :76-100. 被引量:1
  • 4Peschansky V J, Wahlestedt C. Non-coding RNAs as direct and in- direct modulators of epigenetic regulation [ J ]. Epigenetics, 2014,9 (1) :3-12. 被引量:1
  • 5Morlando M, Ballarino M, Fatiea A, et al. The role of long noncod- ing RNAs in the epigenetic control of gene expression [ J ]. Chem Med Chem,2014,9 ( 3 ) :505-510. 被引量:1
  • 6Ji P, Diederichs S, Wang W, et al. MALAT-1, a novel noncoding RNA, and thymosin beta4 predict metastasis and survival in early- stage non-small cell lung cancer [ J ]. Oncogene, 2003,22 ( 39 ) : 8031-8041. 被引量:1
  • 7Lin R, Roychowdhury-Saha M, Black C ,et al. Control of RNA pro- cessing by a large non-coding RNA over-expressed in carcinomas [ J ]. FEBS Lett,2011,585 (4) :671-676. 被引量:1
  • 8Gutschner T, Hgmmerle M,Eissmann M,et al. The noncoding RNA MALAT1 is a critical regulator of the metastasis phenotype of lung cancer ceils[ J]. Cancer Res ,2013,73 (3) :1180-1189. 被引量:1
  • 9Washington K. 7th edition of the AJCC cancer staging manual: stomach [ J ]. Ann Surg 0ncoi,2010,17 ( 12 ) : 3077-3079. 被引量:1
  • 10Livak K J, Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2-aact method [ J ]. Methods,2001,25 (4) :402-408. 被引量:1

二级参考文献10

  • 1Lee J T. Epigenetic regulation by long noncoding RNAs [ J ]. Sci- ence,2012,338 (6113 ) : 1435-1439. 被引量:1
  • 2Timofecva M N, Hung R J, Rafnar T, et al. Influence of common genetic variation on lung cancer risk :recta-analysis of 14 900 cases and 29 485 controls [ J ]. Hum Mol Genet, 2012,21 ( 22 ) : 4980- 4995. 被引量:1
  • 3Guilo F,Zhou M M,Walsh M J. Long noncoding RNA, polycomb, and the ghosts haunting INK4b-ARF-INK4a expression[ J]. Cancer Res ,2011,71 (16) :5365-5369. 被引量:1
  • 4Toh C K. The changing epidemiology of lung cancer [ J ]. Methods Mol Biol, 2009,472 : 397-411. 被引量:1
  • 5Wiggs J L,Yaspan B L,Hauser M A,et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma [ J ]. PLoS Genct,2012,8 (4) : el 002654. 被引量:1
  • 6Congrains A,Kamide K,Oguro R,et al. Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B [ J ]. Atherosclerosis,2012,220 (2) :449-455. 被引量:1
  • 7Iacobucci I, Sazzini M, Garagnani P, et al. A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia posi- tive acute lymphoblastie leukemia [ J ]. Leuk Res, 2011,35 ( 8 ) : 1052-1059. 被引量:1
  • 8Popov N, Gil J. Epigenetie regulation of the INK4b-ARF-INK4a lo- cus :in sickness and in health [ J 1. Epigenetics, 2010,5 ( 8 ) : 685- 690. 被引量:1
  • 9Gutschner T, Diederichs S. The hallmarks of cancer: a long non- coding RNA point of view [ J ]. RNA Biol, 2012,9 ( 6 ) : 703-719. 被引量:1
  • 10Kotake Y, Nakagawa T, Kitagawa K, et al. Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15 ( INK4B ) tumor suppressor gene [ J ]. Oncogene, 2011,30 (16) : 1956-1962. 被引量:1

共引文献3

同被引文献50

  • 1CHEN W G, CHANG Q, LIN Y,et al. Derepression of BDNF tran- scription involves calcium-dependent phosphorylation of MeCP2 [ J ]. Science,2003,302 ( 5646 ) : 885-889. 被引量:1
  • 2FENG J,ZHOU Y,CAMPBELL S L,et al. Dnmtl and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons [ J ]. Nat Neurosci, 2010,13 ( 4 ) :423-430. 被引量:1
  • 3KIMURA A, MATSUBARA K, HORIKOSHI M. A decade of his- tone acetylation: marking eukaryotic chromosomes with specific codes[ J]. J Biochem,2005,138 (6) :647-662. 被引量:1
  • 4CAREY N, LA THANGUE N B. Histone deaeetylase inhibitom: gathefng pace [ J ]. Curr Opin Pharmaol,2006,6 (4) : 369 -375. 被引量:1
  • 5WANG Z, YANG D, ZHANG X, et al. Hypoxia-induced down-reg- ulation of neprilysin by histone modification in mouse primary cor- tical and hippocampal neurons [J]. PLoS One, 2011,6 (4) : e19229. 被引量:1
  • 6MARKS P A. Histone deacetylase inhibitors:a chemical genetics approach to understanding cellular functions [ J ]. Biochim Biophys Acta,2010,1799 (10/11/12) :717-725. 被引量:1
  • 7KUNDAKOVIC M, CHEN Y, GU1DOTTI A, et al. The reelin and GAD67 promoters are activated by epigenetic drugs that facilitate the disruption of local repressor complexes [ J ]. Mol Pharmacol, 2009,75 ( 2 ) : 342 -354. 被引量:1
  • 8FATICA A, BOZZONI I. Long non-coding RNAs:new players incell differentiation and development[ J]. Nat Rev Genet,2014,15 ( 1 ) :7-21. 被引量:1
  • 9KATSAROU K,RAO A L,TSAGRIS M ,et al. Infectious long non- coding RNAs [ J ]. Biochimie ,2015 ,117 : 37-47. 被引量:1
  • 10QURESHI I A, MATFICK J S, MEHLER M F. Long non-coding RNAs in nervous system function and disease [ J ]. Brain Res, 2010,1338:20-35. 被引量:1

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