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肺腺癌患者淋巴转移的分子指纹鉴定 被引量:5

Gene expression signature for lymphatic metastasis of human lung adenocarcinoma
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摘要 背景与目的:远处转移是肺癌患者的重要死因,癌转移可能与细胞内基因表达模式改变有关。急需运用新技术来筛选和分析这些基因,以便进一步阐明癌转移的机制并寻找新的治疗靶点。本研究旨在筛选肺腺癌患者淋巴转移差异表达基因。方法:原发癌组织及区域淋巴结取自22例接受根治性手术的肺腺癌患者。根据组织来源将标本分为三组:不伴淋巴转移的肺腺癌组织(TxN-,n=11)、伴有淋巴转移的肺腺癌组织(TxN+,n=11)及相应转移淋巴结中的肺腺癌细胞(N+,n=11)。对各组进行激光显微切割以获得纯净癌细胞,T7RNA线性扩增获取足够量的RNA,实验通道和参照通道分别标记以后与含6000个已知人类基因或表达序列标签的cDNA基因芯片杂交,扫描荧光信号以后进行数据分析。结果:TxN+组与TxN-组共有17个差异表达基因,其中12个基因表达上调,5个基因表达下调。有53个基因可将N+组与TxN+组区分开,其中在N+组高表达的基因有25个,在TxN+组高表达的有28个。结论:早期癌形成中的遗传学变化和后期癌进展中的获得性分子学变异共同决定肺腺癌的淋巴转移。 Background and Objective: Distant metastasis is a major cause of mortality for patients with lung adenocarcinoma. So far, the mechanism of tumor metastasis is unknown. This study was to screen the gene expression signature in relation to lymphatic metastasis of human lung adenocarcinoma. Methods. Primary lung adenocarcinoma tissues and regional lymph nodes were obtained from 22 patients underwent radical resection. The samples were classified into three groups: 11 cases of primary lung adenocarcinoma without lymphatic metastasis (TxN-), 11 cases of primary lung adenocarcinoma with lymphatic metastasis (TxN+), and 11 cases of the corresponding tumor cells from metastatic lymph nodes(N+). Total RNA was extracted from laser microdissected tumor samples. Adequate RNA starting materials from the primary tumors or metastatic nodes were labeled and then hybridized into the same microarray containing 6000 known human genes or expressed sequence tags (ESTs). After scanning, data analyses were performed using GeneSpringTM 6.2. Results: Among 17 differentially expressed genes between the TxN + and TxN- groups, 12 genes were significantly elevated and five'genes were significantly downregulated in the TxN + group compared with the TxN- group. There were 53 differentially regulated genes between the N+ and TxN+ groups, among which 25 genes were overexpressed and 28 genes were suppressed in the N + group. Conclusion.The combination of early oncogenic alterations and later acquisition of a set of genetic alterations may determine the metastatic potential of lung adenocarcinoma.
出处 《癌症》 SCIE CAS CSCD 北大核心 2009年第3期262-267,共6页 Chinese Journal of Cancer
基金 人事部留学人员科技活动项目(2006) 重庆市科委自然科学基金计划项目(CSTC 2008BB5210)~~
关键词 肺肿瘤 腺细胞癌 淋巴转移 基因表达 分子指纹鉴定 lung adenocarcinoma, gene expression, lymphatic metastasis
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参考文献16

  • 1Ridley A. Molecular switches in metastasis [J]. Nature, 2000,406 (4795) : 466-467.
  • 2Southern E, Mir K, Shchepinov M. Molecular interactions on microarrays [J ]. Nat Genet, 1999,21 ~ 1 Suppl) : 5-9.
  • 3van't Veer LJ, Dai H, van de Vijver M J, et al. Gene expression profiling predicts clinical outcome of breast cancer [J]. Nature, 2002,415(6871 ) :530-536.
  • 4Alizadeh AA, Eisen MB, Davis RE, et al. Distinct types of diffuse large B-cell lymphoma identified by gene-expression profiling [J]. Nature, 2000,403(6769):503-511.
  • 5Vastag B. Gene chips inch toward the clinic [J]. JAMA. 2003289: 155-156,159.
  • 6Groden J, Thliveris A, Samowitz W, et al. Identification and characterization of the familial adenomatous polyposis coli gene [J]. Cell, 1991,66(3) :589-600.
  • 7Polz MF, Cavanaugh CM. Bias in template-to-product ratios in muhitemplate PCR [J]. Appl Environ Microbiol, 1998,64 (10) : 3724-3730.
  • 8Brekken RA, Sullivan MM, Workman G, et al. Expression and characterization of murine hevin (SC1), a member of the SPARC family of matricellular proteins [J]. J Histochem Cytoehem, 2004,52 ( 6 ) : 735-748.
  • 9Huang JB, Kindzelskii AL, Clark AJ, et al. Identification ofchannels promoting calcium spikes and waves in HT1080 tumor cells: their apparent roles in cell motility and invasion [J]. Cancer Res, 2004,64(7) :2482-2489.
  • 10de Lange R, Dimoudis N, Weidle UH. Identification of genes associated with enhanced metastasis of a large cell lung carcinoma cell line [J]. Anticancer Res, 2003,23(1A) : 187- 194.

同被引文献45

  • 1刘东明,许月新,官忠燕,段鸿梅,王恩华,韩昱晨.RhoC及其调节因子RhoGDIβ、RhoGDIγ在肺鳞癌、腺癌中的表达及临床意义[J].中国肺癌杂志,2008,11(4):538-541. 被引量:3
  • 2Hua-Wen Sun Shi-Lun Tong Jie He Qi Wang Li Zou Shu-Jing Ma Hai-Yan Tan Jian-Fei Luo Hong-Xue Wu.RhoA and RhoC -siRNA inhibit the proliferation and invasiveness activity of human gastric carcinoma by Rho/PI3K/Akt pathway[J].World Journal of Gastroenterology,2007,13(25):3517-3522. 被引量:14
  • 3罗海蓉,刘连新,姜洪池.抑癌基因Lumican在胃癌中的表达及其临床意义[J].中国普外基础与临床杂志,2007,14(5):551-553. 被引量:8
  • 4Moseley R,Stewart JE,Stephens P,et al.Extracellular matrix metabolites as potential biomarkers of disease activity in wound fluid:lessons learned from other inflammatory diseases[J]?Br J Dermatol,2004,150(3):401-413.
  • 5Ruoslahti E,Yamaguchi Y.Proteoglycans as modulators of growth factor activities[J].Cell,1991,64(5):867-869.
  • 6Iozzo RV.Matrix pmteoglycans:from molecular design to cellular function[J].Ann Rev Biochem,1998,67:609-652.
  • 7Chakravarti S,Stallings RL,SundarRaj N,et al.Primary structure of human lumican(keratan sulfate proteoglycan)and localization of the gene(LUM)to chromosome 12q21.3-q22[J].Genomics,1995,27:481-488.
  • 8Stephane B,Katarzyna P,Franc X,et al.lumican effects in the control of tumour progression and their links with metalloproteinases and integrins[J].FEBS J,2013,280(10):2369-2381.
  • 9Missan DS,DiPersio M.Integrin control of tumor invasion[J].Crit Rev Eukaryot Gene Expr,2012,22(4):309-324.
  • 10Malinowski M,Pietraszek K,Perreau C,et al.Effect of lumican on the migration of human mesenchymal stem cells and endothelial progenitor cells:involvement of matrix metalloproteinase-14[J].PLoS One,2012,7(12):e50709.

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