Investigation of the molecular changes in patients with multiple myeloma by fluorescence in situ hybridization.
- Author:
Rui-fang YANG
1
;
Chun-ming LI
;
Li-juan CHEN
;
Hai-rong QIU
;
Hui YANG
;
Peng LIU
;
Jia-ren XU
;
Jian-yong LI
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Chromosome Deletion; Chromosomes, Human, Pair 1; genetics; Chromosomes, Human, Pair 13; genetics; Chromosomes, Human, Pair 14; genetics; Female; Gene Deletion; Humans; In Situ Hybridization, Fluorescence; methods; Male; Middle Aged; Multiple Myeloma; genetics; Tumor Suppressor Protein p53; genetics
- From: Chinese Journal of Medical Genetics 2010;27(5):567-570
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the incidence and prognosis of 1q21 amplification, 13q14 deletion, TP53 gene deletion and IgH translocation in patients with multiple myeloma (MM).
METHODSInterphase fluorescence in situ hybridization (I-FISH) with four different specific probes for the regions containing 1q21, 13q14.3 (D13S319), 14q32 and TP53 gene were performed in 43 MM patients.
RESULTSAmong the 43 MM patients, 1q21 amplification was observed in 28 (65.1%) cases, 13q14 deletion in 30 (69.7%) cases, TP53 gene deletion in 8 (18.6%) cases, and IgH translocation in 29 (67.4%) cases. The mortality of MM patients with 1q21 amplification, 13q14 deletion or TP53 gene deletion was higher than those without them.
CONCLUSIONThere is high frequency of 1q21 amplification, 13q14 deletion, TP53 gene deletion and IgH translocation in multiple myeloma, and 1q21 amplification, 13q14 deletion and TP53 gene deletion are poor prognosis factors for MM patients.
