ALLELE-SPECIFIC CHROMOSOME 3P DELETIONS OCCUR AT AN EARLY-STAGE IN THE PATHOGENESIS OF LUNG-CARCINOMA

被引:284
作者
HUNG, J
KISHIMOTO, Y
SUGIO, K
VIRMANI, A
MCINTIRE, DD
MINNA, JD
GAZDAR, AF
机构
[1] UNIV TEXAS,SW MED CTR,SIMMONS CANC CTR,DALLAS,TX 75235
[2] UNIV TEXAS,SW MED CTR,DEPT PATHOL,DALLAS,TX
[3] UNIV TEXAS,SW MED CTR,DEPT INTERNAL MED,DALLAS,TX
[4] UNIV TEXAS,SW MED CTR,DEPT PHARMACOL,DALLAS,TX
[5] UNIV TEXAS,SW MED CTR,ACAD COMP SERV,DALLAS,TX
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1995年 / 273卷 / 07期
关键词
D O I
10.1001/jama.273.7.558
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background.-Deletions in the short arm of chromosome 3 (3p) are present in most lung carcinomas. Objective.-To investigate the role of these chromosome 3p deletions in the pathogenesis of non-small cell lung carcinomas. Design.-Seven archival, paraffin-embedded, surgically resected lung cancer specimens were studied. Fifty precisely identified malignant and preneoplastic lesions present in bronchi, bronchioles, and alveoli were microdissected from stained slides and analyzed for allele loss using polymerase chain reaction-based assays for dinucleotide repeat polymorphisms at three chromosome 3p loci (3p14, 3p21.3, and 3p25). Setting.-University-based medical center and affiliated hospitals. Subjects.-Samples were analyzed from seven patients who underwent surgical resection with curative intent for non-small cell lung cancer and whose specimens included extensive multifocal areas of preneoplastic lesions (hyperplasia, metaplasia, dysplasia, or noninvasive cancer). Results.-Lymphocytes from all seven cases were heterozygous (ie, informative) for all three microsatellites analyzed. Six (86%) of seven invasive cancers had loss of heterozygosity at one or more chromosome 3p sites. In the accompanying preneoplastic lesions, loss of heterozygosity was detected in none of two normal bronchioles, 13 (76%) of 17 hyperplasias, six (86%) of seven dysplasias, and four (100%) of four noninvasive cancers. Loss of heterozygosity was detected throughout the respiratory tract, in bronchi, bronchioles, and alveoli. In 18 (78%) of 23 preneoplastic lesions, the specific alleles lost were identical to those lost in the corresponding carcinomas. The probability of this happening by chance is 5.3x10(-3). Conclusions.-Deletions in the short arm of chromosome 3 occur at the earliest stage (hyperplasia) in the pathogenesis of lung cancer and involve all regions of the respiratory tract. Allele loss is highly specific, but its mechanism remains unknown. Our findings may be of considerable biologic, prognostic, and clinical significance.
引用
收藏
页码:558 / 563
页数:6
相关论文
共 38 条
  • [1] CHANGES IN BRONCHIAL EPITHELIUM IN RELATION TO CIGARETTE-SMOKING, 1955-1960 VS 1970-1977
    AUERBACH, O
    HAMMOND, EC
    GARFINKEL, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1979, 300 (08) : 381 - 386
  • [2] MOLECULAR ANALYSIS OF THE SHORT ARM OF CHROMOSOME-3 IN SMALL-CELL AND NON-SMALL-CELL CARCINOMA OF THE LUNG
    BRAUCH, H
    JOHNSON, B
    HOVIS, J
    YANO, T
    GAZDAR, A
    PETTENGILL, OS
    GRAZIANO, S
    SORENSON, GD
    POIESZ, BJ
    MINNA, J
    LINEHAN, M
    ZBAR, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (18) : 1109 - 1113
  • [3] MOLECULAR MAPPING OF DELETION SITES IN THE SHORT ARM OF CHROMOSOME-3 IN HUMAN LUNG-CANCER
    BRAUCH, H
    TORY, K
    KOTLER, F
    GAZDAR, AF
    PETTENGILL, OS
    JOHNSON, B
    GRAZIANO, S
    WINTON, T
    BUYS, CHCM
    SORENSON, GD
    POIESZ, BJ
    MINNA, JD
    ZBAR, B
    [J]. GENES CHROMOSOMES & CANCER, 1990, 1 (03) : 240 - 246
  • [4] ALLELE-SPECIFIC ACTIVATION AND EXPRESSION OF THE K-RAS GENE IN HYBRID MOUSE LUNG-TUMORS INDUCED BY CHEMICAL CARCINOGENS
    CHEN, B
    YOU, L
    WANG, Y
    STONER, GD
    YOU, M
    [J]. CARCINOGENESIS, 1994, 15 (09) : 2031 - 2035
  • [5] PREFERENTIAL AMPLIFICATION OF THE PATERNAL ALLELE OF THE N-MYC GENE IN HUMAN NEUROBLASTOMAS
    CHENG, JM
    HIEMSTRA, JL
    SCHNEIDER, SS
    NAUMOVA, A
    CHEUNG, NKV
    COHN, SL
    DILLER, L
    SAPIENZA, C
    BRODEUR, GM
    [J]. NATURE GENETICS, 1993, 4 (02) : 191 - 194
  • [6] DALY MC, 1993, ONCOGENE, V8, P1271
  • [7] GENOMIC IMPRINTING AND GENE ACTIVATION IN CANCER
    FEINBERG, AP
    [J]. NATURE GENETICS, 1993, 4 (02) : 110 - 113
  • [8] FERGUSONSMITH AC, 1990, CANCER SURV, V9, P487
  • [9] GAZDAR AF, 1994, BIOL GENETICS LUNG C
  • [10] GREENBERG SD, 1987, LUNG CARCINOMAS, P287