Mutation analysis of the PTEN/MMAC1 gene in lung cancer

被引:162
作者
Forgacs, E
Biesterveld, EJ
Sekido, Y
Fong, K
Muneer, S
Wistuba, II
Milchgrub, S
Brezinschek, R
Virmani, A
Gazdar, AF
Minna, JD
机构
[1] Univ Texas, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dept Internal Med, Dallas, TX 75235 USA
[2] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75235 USA
[3] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75235 USA
关键词
homozygous deletion; loss of heterozygosity; chromosome; 10q23;
D O I
10.1038/sj.onc.1202070
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
We studied PTEN/MMAC1, a newly discovered candidate tumor suppressor gene at 10q23.3, for mutations in lung cancer. One hundred and thirty-six lung cancer cell line DNAs (66 small cell lung cancers, SCLC, 61 non-small cell lung cancers, NSCLC, four mesotheliomas, five extrapulmonary small cell cancers) were analysed for PTEN/MMAC1 homozygous deletions and five (8%) SCLC lines showed homozygous deletions interrupting the PTEN/MMAC1 gene. Using single stranded conformation polymorphism (SSCP) analysis, we screened the PTEN/MMAC1 open reading frame of 53 lung cancer cell line cDNAs for point mutations and found that 3/35 SCLCs and 3/18 NSCLCs contained homozygous amino acid sequence altering mutations. Northern blot analysis revealed that expression of the PTEN/MMAC1 gene was considerably lower in all the tumor cell lines with point mutations while no expression was detected for cell lines with PTEN/MMAC1 homozygous deletions. Mutation analysis of 22 uncultured, microdissected, primary SCLC tumors and metastases showed two silent mutations, and two apparent homozygous deletions. We also discovered a processed pseudogene (PTEN2) which has 98.5% nt identity to PTEN/MMAC1, that needs to be accounted for in cDNA mutation analysis, Our findings suggest that genetic abnormalities of the PTEN/MMAC1 gene are only involved in a relatively small subset of lung cancers.
引用
收藏
页码:1557 / 1565
页数:9
相关论文
共 32 条
  • [1] Arch EM, 1997, AM J MED GENET, V71, P489, DOI 10.1002/(SICI)1096-8628(19970905)71:4<489::AID-AJMG24>3.3.CO
  • [2] 2-I
  • [3] Boström J, 1998, CANCER RES, V58, P29
  • [4] Dahia PLM, 1997, CANCER RES, V57, P4710
  • [5] TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION
    DON, RH
    COX, PT
    WAINWRIGHT, BJ
    BAKER, K
    MATTICK, JS
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (14) : 4008 - 4008
  • [6] MUTATION OF THE MXI1 GENE IN PROSTATE-CANCER
    EAGLE, LR
    YIN, XY
    BROTHMAN, AR
    WILLIAMS, BJ
    ATKIN, NB
    PROCHOWNIK, EV
    [J]. NATURE GENETICS, 1995, 9 (03) : 249 - 255
  • [7] Allele loss in colorectal cancer at the Cowden disease juvenile polyposis locus on 10q
    Frayling, IM
    Bodmer, WF
    Tomlinson, IPM
    [J]. CANCER GENETICS AND CYTOGENETICS, 1997, 97 (01) : 64 - 69
  • [8] Growth suppression of glioma cells by PTEN requires a functional phosphatase catalytic domain
    Furnari, FB
    Lin, H
    Huang, HJS
    Cavenee, WK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (23) : 12479 - 12484
  • [9] Guldberg P, 1997, CANCER RES, V57, P3660
  • [10] ALLELE-SPECIFIC CHROMOSOME 3P DELETIONS OCCUR AT AN EARLY-STAGE IN THE PATHOGENESIS OF LUNG-CARCINOMA
    HUNG, J
    KISHIMOTO, Y
    SUGIO, K
    VIRMANI, A
    MCINTIRE, DD
    MINNA, JD
    GAZDAR, AF
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (07): : 558 - 563