Detection of eIF4E gene amplification in breast cancer by competitive PCR

被引:44
作者
Sorrells, DL
Black, DR
Meschonat, C
Rhoads, R
De Benedetti, A
Gao, MX
Williams, BJ
Li, BDL
机构
[1] Louisiana State Univ, Med Ctr, Sect Surg Oncol, Dept Surg, Shreveport, LA 71130 USA
[2] Louisiana State Univ, Med Ctr, Dept Biochem, Shreveport, LA 71130 USA
[3] Louisiana State Univ, Med Ctr, Dept Urol, Shreveport, LA 71130 USA
关键词
eIF4E; amplification; breast; cancer; competitive PCR;
D O I
10.1007/BF02303778
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Initiation factor eIF3E binds to mRNA as the initial step for protein translation. Overexpression of the eIF3E oncoprotein has been found in breast cancer but not in benign breast tissue. The objective of this study is to determine if eIF3E oncoprotein overexpression is associated with elF4E gene amplification in breast cancer using Western blots and competitive polymerase chain reaction (PCR). Methods: Unknown concentrations of DNA extracted from breast specimens were amplified by PCR using a set of primers spanning intron 2/exon 3 of the eIF4E gene. In the same PCR tube, an internal control consisting of a known concentration of an eIF4E DNA template with 20-base pair (bp) deletion was used as the competitive reference standard (CRS) for competitive PCR. Gel electrophoresis of the PCR products was performed and the bands quantified by densitometry. eIF4E gene amplification was then determined relative to a nonamplified gene (gastrin). Using an anti-eIF4E rabbit antibody, Western blots were performed on benign and malignant breast specimens. Quantification was accomplished by developing blots with a color assay using nitro blue tetrazolium (NBT) and 5-bromo-3-chloro-3-indolyl phosphate (BCIP), scanned and analyzed by densitometry. Results: Twenty-two breast specimens (14 cancer, 8 control) from patients were examined for eIF4E gene amplification and oncoprotein expression. In all fourteen specimens from stage I-III breast cancer patients, eIF4E overexpression was detected at 3- to 30-fold (16.71 +/- 7.83) elevations. Similarly, all 14 specimens demonstrated eIF4E gene amplification by competitive PCR (3.69 +/- 1.27). In the eight benign breast specimens examined, all were negative for eIF4E overexpression and gene amplification. Conclusions: Overexpression of eINE was associated with elF4E gene amplification in breast cancer specimens. No overexpression or gene amplification was detected in benign breast tissues. elF4E gene amplification may be one mechanism for eIF4E oncoprotein overexpression.
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收藏
页码:232 / 237
页数:6
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