Expression profiling of primary non-small cell lung cancer for target identification

被引:128
作者
Heighway, J
Knapp, T
Boyce, L
Brennand, S
Field, JK
Betticher, DC
Ratschiller, D
Gugger, M
Donovan, M
Lasek, A
Rickert, P
机构
[1] Univ Liverpool, Roy Castle Int Ctr Lung Canc Res, Target Identificat Grp, Liverpool, Merseyside, England
[2] Univ Bern, Inst Med Oncol, CH-3010 Bern, Switzerland
[3] Incyte Genom Inc, Palo Alto, CA 94304 USA
关键词
lung; cancer; microarray; expression; target identification;
D O I
10.1038/sj.onc.1205979
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using a panel of cDNA microarrays comprising 47 650 transcript elements, we have carried out a dual-channel analysis of gene expression in 39 resected primary human non-small cell lung tumours versus normal lung tissue. Whilst similar to11000 elements were scored as differentially expressed at least twofold in at least one sample, 96 transcripts were scored as over-represented fourfold or more in at least seven out of 39 tumours and 30 sequences 16-fold in at least two out of 39 tumours, including 24 transcripts in common. Transcripts (178) were found under-represented fourfold in at least seven out of 39 tumours, 31 of which are under-represented 16-fold in at least two out of 39 lesions. The relative expression levels of representative genes from these lists were analysed by comparative multiplex RT-PCR and found to be broadly consistent with the microarray data. Two dramatically over-represented genes, previously designated as potential tumour suppressors in breast (maspin) and lung and breast (S100A2) cancers, were analysed more extensively and demonstrate the effectiveness of this approach in identifying potential lung cancer diagnostic or therapeutic targets. Whilst it has been reported that S100A2 is downregulated in NSCLC at an early stage, our microarray, cmRT-PCR, Western and immunohistochemistry data indicate that it is strongly expressed in the majority of tumours.
引用
收藏
页码:7749 / 7763
页数:15
相关论文
共 35 条
  • [1] Agrawal D, 2002, J NATL CANCER I, V94, P513
  • [2] Gene expression profiling of cancer by use of DNA arrays: how far from the clinic?
    Bertucci, F
    Houlgatte, R
    Nguyen, C
    Viens, P
    Jordan, BR
    Birnbaum, D
    [J]. LANCET ONCOLOGY, 2001, 2 (11) : 674 - 682
  • [3] Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses
    Bhattacharjee, A
    Richards, WG
    Staunton, J
    Li, C
    Monti, S
    Vasa, P
    Ladd, C
    Beheshti, J
    Bueno, R
    Gillette, M
    Loda, M
    Weber, G
    Mark, EJ
    Lander, ES
    Wong, W
    Johnson, BE
    Golub, TR
    Sugarbaker, DJ
    Meyerson, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) : 13790 - 13795
  • [4] Matrix metalloproteinases and matrix metalloproteinase inhibitors in lung cancer
    Bonomi, P
    [J]. SEMINARS IN ONCOLOGY, 2002, 29 (01) : 78 - 86
  • [5] Estimates of cancer incidence and mortality in Europe in 1995
    Bray, F
    Sankila, R
    Ferlay, J
    Parkin, DM
    [J]. EUROPEAN JOURNAL OF CANCER, 2002, 38 (01) : 99 - 166
  • [6] Feng G, 2001, CANCER RES, V61, P7999
  • [7] Cancer: looking outside the genome
    Folkman, J
    Hahnfeldt, P
    Hlatky, L
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) : 76 - 79
  • [8] FRAIRE AE, 1987, CANCER, V60, P370, DOI 10.1002/1097-0142(19870801)60:3<370::AID-CNCR2820600314>3.0.CO
  • [9] 2-W
  • [10] Diversity of gene expression in adenocarcinoma of the lung
    Garber, ME
    Troyanskaya, OG
    Schluens, K
    Petersen, S
    Thaesler, Z
    Pacyna-Gengelbach, M
    van de Rijn, M
    Rosen, GD
    Perou, CM
    Whyte, RI
    Altman, RB
    Brown, PO
    Botstein, D
    Petersen, I
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) : 13784 - 13789