Analysis of 13q14 chromosomal instability in soft tissue tumors by fluorescence in-situ hybridization.
- Author:
Wei-xun ZHOU
1
;
Xuan ZENG
;
Tong-hua LIU
;
Sha-fei WU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Aged; Chromosomal Instability; Chromosomes, Human, Pair 13; Female; Gastrointestinal Stromal Tumors; genetics; Humans; In Situ Hybridization, Fluorescence; Loss of Heterozygosity; Male; Middle Aged; Retroperitoneal Neoplasms; genetics; Soft Tissue Neoplasms; genetics; Young Adult
- From: Chinese Journal of Pathology 2007;36(9):582-586
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the genetic status of 13q and its role in the oncogenesis and progress of soft tissue tumors.
METHODSForty-one soft tissue tumors, including 9 benign tumors, 9 tumors of malignant potential and 23 sarcomas, were studied by fluorescence in-situ hybridization (FISH) using dual color probes. The probes were generated from BAC clones RP11-685I15, RP11-352N7 and RP11-505F3, corresponding to Rb, RFP2, KCNRG and KLF5 genes respectively.
RESULTSLoss of heterozygosity (LOH) of RP11-685I15 were found in 8/41 cases, LOH of RP11-352N7 was seen in 4/41 cases and LOH of RP11-505F3 was present in 3/41 cases. LOH of all 3 loci were detected in 2 cases. LOH of RP11-61K9, an internal control locus, was detected in 2 cases. One case of malignant peripheral nerve sheath tumor showed amplification at all 3 loci. Amplification of RP11-505F3 was seen in another 2 cases.
CONCLUSIONSA significant percentage of soft tissue tumors exhibited chromosomal instability, reflected by an increase of LOH at tumor-suppressing gene loci. The incidence of 13q abnormality was different in various types of soft tissue tumors, indicating that alterations of Rb, RFP2, KCNRG and KLF5 tumor suppressing genes may play diverse roles in different types of soft tissue tumor.
