Evaluation on parallel HER-2 testing using in situ hybridization and immunohistochemistry in breast cancer tissues.
- Author:
Xiao-Ying PAN
1
;
Hong-Yi GAO
;
Jia-Li ZHANG
;
Wen-Ting FU
;
Shu LIU
Author Information
- Publication Type:Journal Article
- MeSH: Breast Neoplasms; genetics; metabolism; Carcinoma, Ductal, Breast; genetics; metabolism; Female; Humans; Immunohistochemistry; In Situ Hybridization, Fluorescence; Receptor, ErbB-2; analysis; genetics
- From: Journal of Southern Medical University 2009;29(11):2225-2227
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the application of the immunohistochemistry (IHC) and the fluorescence in situ hybridization (FISH) in detecting the amplification and the expression of HER-2 gene in the breast cancer patients.
METHODSSixty-six cases of paraffin-embeded breast cancer samples with overexpression, low or no expression of HER-2 gene as detected by IHC were analyzed for HER-2 gene amplification using FISH.
RESULTSAmong the 42 samples with HER-2 gene overexpression (3+/2+) detected by IHC, 31 showed positive HER-2 gene amplification and 11 showed negative HER-2 gene amplification in FISH. In the 24 samples with low or no HER-2 gene expression (1+/-) detected by IHC, no HER-2 gene amplification was detected by FISH. The results of the two testing methods showed a good consistency with the kappa coefficient of 0.672 (P<0.001). We also found that the 17 chromosome polysomy in 42% of the samples and the incidence of 17 polysomy was significantly higher in the HER-2 gene overexpression (3+/2+) group than in low or no HER-2 gene expression (1+/-) group (chi(2)=4.688, P=0.03).
CONCLUSIONIHC can be used as a screening method for detecting HER-2 gene amplification, and FISH should be performed in cases of HER-2 gene overexpression (3+/2+) as detected by IHC.