DELETIONS OF THE CYCLIN-DEPENDENT KINASE INHIBITOR GENES P16(INK4A) AND P15(INK4B) IN NON-HODGKINS-LYMPHOMAS

被引:73
作者
GOMBART, AF [1 ]
MOROSETTI, R [1 ]
MILLER, CW [1 ]
SAID, JW [1 ]
KOEFFLER, HP [1 ]
机构
[1] CEDARS SINAI MED CTR,DIV HEMATOPATHOL,LOS ANGELES,CA 90048
关键词
D O I
10.1182/blood.V86.4.1534.bloodjournal8641534
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The tumor suppressor genes p16(INK4A) and p15(INK4B) map to the 9p21 chromosomal locus and are either homozygously deleted or mutated in a wide range of human cancer cell lines and tumors, Although chromosome 9 abnormalities have been described in non-Hodgkin's lymphomas (NHLs), to date, the mutational status of these genes has not been determined for these malignancies. A total of five cell lines and 75 NHLs were examined for homozygous deletions or point mutations in the coding regions of both the p15 and p16 genes using Southern blot and/or polymerase chain reaction-single-strand conformation polymorphism analyses. Homozygous deletions of either the p16 gene or both the p15 and p16 genes were observed in one diffuse large B-cell lymphoma cell line and two uncultured lymphomas consisting of one large B-cell and one mixed T-cell lymphoma. In contrast, point mutations were not detected in either the cell lines or lymphomas. These results indicate that the rate of alterations in the p15 and p16 genes is low for lymphomas, but loss of p16 and/or p15 may be involved in the development of some lymphomas. (C) 1995 by The American Society of Hematology.
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收藏
页码:1534 / 1539
页数:6
相关论文
共 60 条
[11]   P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST [J].
HANNON, GJ ;
BEACH, D .
NATURE, 1994, 371 (6494) :257-261
[12]  
HARPER JW, 1993, CELL, V75, P805
[13]   SOMATIC MUTATIONS OF THE MTS (MULTIPLE TUMOR-SUPPRESSOR)-1 CDK41 (CYCLIN-DEPENDENT KINASE-4 INHIBITOR) GENE IN HUMAN PRIMARY NONSMALL CELL LUNG CARCINOMAS [J].
HAYASHI, N ;
SUGIMOTO, Y ;
TSUCHIYA, E ;
OGAWA, M ;
NAKAMURA, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (03) :1426-1430
[14]  
HE J, 1994, CANCER RES, V54, P5804
[15]   CANDIDATE TUMOR-SUPPRESSOR GENES MTS1 (P16(INK4A)) AND MTS2 (P15(INK4B)) DISPLAY FREQUENT HOMOZYGOUS DELETIONS IN PRIMARY-CELLS FROM T-CELL BUT NOT FROM B-CELL LINEAGE ACUTE LYMPHOBLASTIC LEUKEMIAS [J].
HEBERT, J ;
CAYUELA, JM ;
BERKELEY, J ;
SIGAUX, F .
BLOOD, 1994, 84 (12) :4038-4044
[16]   A CELL-CYCLE-REGULATED INHIBITOR OF CYCLIN-DEPENDENT KINASES [J].
HENGST, L ;
DULIC, V ;
SLINGERLAND, JM ;
LEES, E ;
REED, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5291-5295
[17]   FUNCTION OF A HUMAN CYCLIN GENE AS AN ONCOGENE [J].
HINDS, PW ;
DOWDY, SF ;
EATON, EN ;
ARNOLD, A ;
WEINBERG, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :709-713
[18]   TUMOR-SUPPRESSOR GENES [J].
HINDS, PW ;
WEINBERG, RA .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) :135-141
[19]   BRAKING THE CYCLE [J].
HUNTER, T .
CELL, 1993, 75 (05) :839-841
[20]   CYCLINS AND CANCER .2. CYCLIN-D AND CDK INHIBITORS COME OF AGE [J].
HUNTER, T ;
PINES, J .
CELL, 1994, 79 (04) :573-582