Stability of microsatellites in myeloid neoplasias

被引:17
作者
Boyer, JC
Risinger, JI
Farber, RA
机构
[1] Univ N Carolina, Dept Pathol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Res Ctr, Chapel Hill, NC 27599 USA
[4] NIEHS, Mol Carcinogenesis Lab, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1016/S0165-4608(98)00043-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microsatellites are short, repeated DNA sequences that exist throughout the genome. Instability of these sequences, associated with defects in the DNA mismatch repair system, is the hallmark of hereditary non-polyposis colorectal cancer (HNPCC), and is also found in many sporadic cancers. Although many types of solid tumors exhibit this type of genetic instability, its involvement in hematologic cancers is less evident. We have investigated whether microstatellite instability (MSI) is involved in the transformation of myeloid cells to myelodysplastic syndrome (MDS) and/or acute myelogenous leukemia (AML). Both de novo and treatment-associated neoplasias were studied. Only one example of MSI was found in 48 patients, using a panel of 14 different microsatellite loci consisting of repeats of one to four base pairs. These results suggest that the genes responsible for MSI are not involved in the transformation of normal myeloid cells to MDS or AML. (C) Elsevier Science, Inc., 1998.
引用
收藏
页码:54 / 61
页数:8
相关论文
共 51 条
[1]   Microsatellite instability in childhood T cell acute lymphoblastic leukemia [J].
Baccichet, A ;
Benachenhou, N ;
Couture, F ;
Leclerc, JM ;
Sinnett, D .
LEUKEMIA, 1997, 11 (06) :797-802
[2]   Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over [J].
Baker, SM ;
Plug, AW ;
Prolla, TA ;
Bronner, CE ;
Harris, AC ;
Yao, X ;
Christie, DM ;
Monell, C ;
Arnheim, N ;
Bradley, A ;
Ashley, T ;
Liskay, RM .
NATURE GENETICS, 1996, 13 (03) :336-342
[3]   MALE-MICE DEFECTIVE IN THE DNA MISMATCH REPAIR GENE PMS2 EXHIBIT ABNORMAL CHROMOSOME SYNAPSIS IN MEIOSIS [J].
BAKER, SM ;
BRONNER, CE ;
ZHANG, L ;
PLUG, AW ;
ROBATZEK, M ;
WARREN, G ;
ELLIOTT, EA ;
YU, JA ;
ASHLEY, T ;
ARNHEIM, N ;
FLAVELL, RA ;
LISKAY, RM .
CELL, 1995, 82 (02) :309-319
[4]   MICROSATELLITE INSTABILITY IN PRIMARY NEOPLASMS FROM HIV+ PATIENTS [J].
BEDI, GC ;
WESTRA, WH ;
FARZADEGAN, H ;
PITHA, PM ;
SIDRANSKY, D .
NATURE MEDICINE, 1995, 1 (01) :65-68
[5]  
BenYehuda D, 1996, BLOOD, V88, P4296
[6]  
CROSS NCP, 1994, BLOOD, V84, P3236
[7]  
Datta A, 1996, MOL CELL BIOL, V16, P1085
[8]   A CELLULAR ONCOGENE IS TRANSLOCATED TO THE PHILADELPHIA-CHROMOSOME IN CHRONIC MYELOCYTIC-LEUKEMIA [J].
DEKLEIN, A ;
VANKESSEL, AG ;
GROSVELD, G ;
BARTRAM, CR ;
HAGEMEIJER, A ;
BOOTSMA, D ;
SPURR, NK ;
HEISTERKAMP, N ;
GROFFEN, J ;
STEPHENSON, JR .
NATURE, 1982, 300 (5894) :765-767
[9]   INACTIVATION OF THE MOUSE MSH2 GENE RESULTS IN MISMATCH REPAIR DEFICIENCY, METHYLATION TOLERANCE, HYPERRECOMBINATION, AND PREDISPOSITION TO CANCER [J].
DEWIND, N ;
DEKKER, M ;
BERNS, A ;
RADMAN, M ;
RIELE, HT .
CELL, 1995, 82 (02) :321-330
[10]  
Eshleman James R., 1995, Current Opinion in Oncology, V7, P83