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PANDER基因在胃癌中的表达下调 被引量:4

Down-regulation of PANDER mRNA in gastric cancer
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摘要 目的:研究配对胃癌组织及转移淋巴结组织中中PANDER基因表达,并分析其与胃癌临床病理及预后的相关性.方法:用RT-PCR检测22例配对胃癌及对应切缘正常胃黏膜组织中PANDER mRNA的表达;制备PANDER cRNA探针,并构建胃癌组织芯片,用原位杂交方法检测208例配对的胃癌组织及转移淋巴结中PANDER基因的表达,分析PANDER基因表达与胃癌临床病理及预后之间的相关性.结果:RT-PCR显示16/22例(72.7%)胃癌中PANDER基因表达下降.原位杂交证实从正常胃黏膜至转移淋巴结,PANDER阳性率依次降低(χ2=81.135,P=0.00).PANDER基因在60.9%胃癌组织中表达下降,早期胃癌与进展期胃癌表达下降的比率无差别(χ2=5.362,P=0.147).肿瘤组织PANDER基因表达与浸润深度有关,局限在黏膜和黏膜下层浸润者PANDER表达高于已经浸润至肌层和浆膜层者(Z=-2.52,P=0.012);胃癌组织中PANDER基因表达与胃癌预后无关.结论:胃癌组织中PANDER表达的下降是胃癌早期事件,可能与胃癌的发生、发展相关. AIM: To investigate the expression of PANDER gene in paired gastric cancer tissues and metastatic lymphatic tissues, and to evaluate its relationship with the clinicopathologic characteristics and disease prognosis. METHODS: Reverse transcription-polymerase chain reaction (RT-PCR) was used to examine the expression of PANDER mRNA in 22 fresh surgical samples of primary gastric cancer tissues and their paired surrounding normal gastric mucosa. A gastric cancer tissue microarray containing 1020 duplicate matched normal mucosa, malignant tissues and metastatic lymphatic tissues from 208 gastric cancer patients was constructed. In situ hybridization analysis was performed on the tissue microarray and the correlation between PANDER mRNA expression and clinicopathologic factors was analyzed. RESULTS: RT-PCR showed that the expression of PANDER mRNA decreased in 72.7% (16/22) of gastric cancer samples. Similar results were obtained by in situ hybridization analysis (60.9%, 112/184). The expression of PANDER mRNA showed an ordinally decreasing trend in the matched normal mucosa, tumor tissues and metastatic lymphatic tissues (x^2 = 81.135, P = 0.00). There was no difference between early gastric cancer and progressive gastric cancer (x^2 = 5.362, P = 0.147). In tumor tissues, lower expression of PANDER mRNA was associated with deeper invasion (Z = -2.52, P = 0.012). There was no correlation between PANDER mRNA expression and disease prognosis. CONCLUSION: Down-regulation of PANDER gene expression occurs at the early stage of gastric cancer, which may be involved in the genesis and development of gastric cancer.
出处 《世界华人消化杂志》 CAS 北大核心 2008年第14期1513-1518,共6页 World Chinese Journal of Digestology
基金 国家自然科学基金资助项目 No.30600728~~
关键词 胃癌 逆转录-聚合酶链反应 组织芯片 原位杂交 PANDER基因 Gastric cancer Reverse transcriptionpolymerase chain reaction Tissue microarray In situ hybridization PANDER mRNA
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参考文献7

  • 1杨少波,王孟薇,邵勇,吴本俨,胡庚熙,尤纬缔.胃腺癌差异表达基因的cDNA微阵列研究[J].肿瘤防治杂志,2005,12(8):571-575. 被引量:6
  • 2邵勇,杨少波,王孟薇,吴本俨,尤纬缔,李红.胃癌基因表达谱的cDNA微阵列与聚类分析[J].中华医学遗传学杂志,2004,21(2):110-115. 被引量:10
  • 3Zhu Y,Xu G,Patel A,McLaughlin MM,Silverman C,Knecht K,Sweitzer S,Li X,McDonnell P,Mirabile R,Zimmerman D,Boyce R,Tierney LA,Hu E,Livi GP,Wolf B,Abdel-Meguid SS,Rose GD,Aurora R,Hensley P,Briggs M,Young PR.Cloning,expression,and initial characterization of a novel cytokine-like gene family.Genomics 2002;80:144-150
  • 4Cao X,Gao Z,Robert CE,Greene S,Xu G,Xu W,Bell E,Campbell D,Zhu Y,Young R,Trucco M,Markmann JF,Naji A,Wolf BA.Pancreatic-derived factor (FAM3B),a novel islet cytokine,induces apoptosis of insulin-secreting beta-cells.Diabetes 2003;52:2296-2303
  • 5Cao X,Yang J,Burkhardt BR,Gao Z,Wong RK,Greene SR,Wu J,Wolf BA.Effects of overexpression of pancreatic derived factor (FAM3B) in isolated mouse islets and insulin-secreting betaTC3 cells.Am J Physiol Endocrinol Metab 2005;289:E543-E550
  • 6Burkhardt BR,Greene SR,White P,Wong RK,Brestelli JE,Yang J,Robert CE,Brusko TM,Wasserfall CH,Wu J,Atkinson MA,Gao Z,Kaestner KH,Wolf BA.PANDER-induced cell-death genetic networks in islets reveal central role for caspase-3 and cyclin-dependent kinase inhibitor 1A (p21).Gene 2006;369:134-141
  • 7Yang J,Gao Z,Robert CE,Burkhardt BR,Gaweska H,Wagner A,Wu J,Greene SR,Young RA,Wolf BA.Structure-function studies of PANDER,an islet specific cytokine inducing cell death of insulin-secreting beta cells.Biochemistry 2005;44:11342-11352

二级参考文献31

  • 1Wan J, Zhang ZQ, Zhu C, et al. Evaluation of the clinical screening and the follow-up for early gastric cancer by gastroscopy in the elderly. Chin J Geriatr, 2001, 20∶103-104.[万军, 张子其, 朱成, 等. 胃镜普查及随访对老
  • 2Quackenbush J. Microarray data normalization and transformation. Nat Genetics, 2002, 32 (suppl)∶496-501.
  • 3Eisen MB, Spellman PT, Brown PO, et al. Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci U S A, 1998, 95∶14863-14868.
  • 4Tusher VG, Tibshirani R, Chu G. Significance analysis of microarrays applied to the ionizing radiation response. Proc Natl Acad Sci U S A, 2001, 98∶5116-5121.
  • 5Xiao Y, Segal MR, Rabert D, et al. Assessment of differential gene expression in human peripheral nerve injury. BMC Genomics, 2002, 3∶28.
  • 6Hippo Y, Taniguchi H, Tsutsumi S, et al. Global gene expression analysis of gastric cancer by oligonucleotide microarrays. Cancer Res, 2002, 62, 233-240.
  • 7Sorlie T, Perou CM, Tibshirani R, et al. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci U S A, 2001, 98∶10869-10874.
  • 8Moschos SJ, Mantzoros CS. The role of the IGF system in cancer: from basic to clinical studies and clinical applications. Oncology, 2002, 63∶317-332.
  • 9Wu MS, Wang HP, Lin CC, et al. Loss of imprinting and overexpression of IGF2 gene in gastric adenocarcinoma. Cancer Lett, 1997, 120∶9-14.
  • 10Yi HK, Hwang PH, Yang DH, et al. Expression of the insulin-like growth factors (IGFs) and the IGF-binding proteins (IGFBPs) in human gastric cancer cells. Eur J Cancer, 2001, 37∶2257-2263.

共引文献13

同被引文献36

  • 1邵勇,杨少波,王孟薇,吴本俨,尤纬缔,李红.胃癌基因表达谱的cDNA微阵列与聚类分析[J].中华医学遗传学杂志,2004,21(2):110-115. 被引量:10
  • 2Mukhopadhyay A, Ni J, Zhai Y, et al. Identification and characterization of a novel cytokine, THANK, a TNF homologue that activates apoptosis, nuclear factor-κB, and cJun NH2-terminal kinase. J Biol Chem, 1999, 274 (23): 15978-81
  • 3Blumberg H, Conklin D, Xu WF, et al. Interleukin 20: discovery, receptor identification, and role in epidermal function. Cell, 2001, 104 (1): 9-19
  • 4Nicola N. Guidebook to cytokines and their receptors. New York: Oxford University Press, 1994
  • 5Abdel-Meguid SS, Shieh HS, Smith WW, et al. Three-dimensional structure of a genetically engineered variant of porcine growth hormone. Proc Natl Acad Sci USA, 1987, 84 (18): 6434-7
  • 6Aurora R, Rose GD. Seeking an ancient enzyme in methanococcus jannaschii.using ORF, a program based on predicted secondary structure comparisons. Proc Natl Acad Sci USA, 1998, 95 (6): 2818-23
  • 7Zhu Y, Xu G, Patel A, et al. Cloning, expression, and initial characterization of a novel cytokine-like gene family. Genomics, 2002, 80 (2): 144-50
  • 8Bione S, Tamanini F, Maestrini E, et al. Transcriptional organization of a 450-kb region of the human chromosome in Xq28. Proc Natl Acad Sci USA, 1993, 90 (23): 10977-81
  • 9Pilipenko VV, Reece A, Choo DI, et al. Genornic organization and expression analysis of the murine Fam3c gene. Gene, 2004, 335:159-68
  • 10Guo JH, Cheng HP, Zhao SY, et al. GG: a domain involved in phage LTF apparatus and implicated in human MEB and non-syndromic hearing loss diseases. FEBS Lett, 2006, 580 (2): 581-4

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