A novel amplicon at 8p22–23 results in overexpression of cathepsin B in esophageal adenocarcinoma
- 13 October 1998
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 95 (21) , 12410-12415
- https://doi.org/10.1073/pnas.95.21.12410
Abstract
Cathepsin B ( CTSB ) is overexpressed in tumors of the lung, prostate, colon, breast, and stomach. However, evidence of primary genomic alterations in the CTSB gene during tumor initiation or progression has been lacking. We have found a novel amplicon at 8p22–23 that results in CTSB overexpression in esophageal adenocarcinoma. Amplified genomic Not I– Hin fI fragments were identified by two-dimensional DNA electrophoresis. Two amplified fragments (D4 and D5) were cloned and yielded unique sequences. Using bacterial artificial chromosome clones containing either D4 or D5, fluorescent in situ hybridization defined a single region of amplification involving chromosome bands 8p22–23. We investigated the candidate cancer-related gene CTSB , and potential coamplified genes from this region including farnesyl-diphosphate farnesyltransferase ( FDFT1 ), arylamine N- acetyltransferase ( NAT-1 ), lipoprotein lipase ( LPL ), and an uncharacterized expressed sequence tag (D8S503). Southern blot analysis of 66 esophageal adenocarcinomas demonstrated only CTSB and FDFT1 were consistently amplified in eight (12.1%) of the tumors. Neither NAT-1 nor LPL were amplified. Northern blot analysis showed overexpression of CTSB and FDFT1 mRNA in all six of the amplified esophageal adenocarcinomas analyzed. CTSB mRNA overexpression also was present in two of six nonamplified tumors analyzed. However, FDFT1 mRNA overexpression without amplification was not observed. Western blot analysis confirmed CTSB protein overexpression in tumor specimens with CTSB mRNA overexpression compared with either normal controls or tumors without mRNA overexpression. Abundant extracellular expression of CTSB protein was found in 29 of 40 (72.5%) of esophageal adenocarcinoma specimens by using immunohistochemical analysis. The finding of an amplicon at 8p22–23 resulting in CTSB gene amplification and overexpression supports an important role for CTSB in esophageal adenocarcinoma and possibly in other tumors.Keywords
This publication has 33 references indexed in Scilit:
- GAC1, a new member of the leucine-rich repeat superfamily on chromosome band 1q32.1, is amplified and overexpressed in malignant gliomasOncogene, 1998
- Molecular cloning of a novel receptor (CMKLR1) with homology to the chemotactic factor receptorsCytogenetic and Genome Research, 1996
- Molecular Cloning and Functional Analysis of the Promoter of the Human Squalene Synthase GeneJournal of Biological Chemistry, 1995
- Immunohistochemical localization of cathepsin B in neoplastic human prostateThe Prostate, 1995
- High yield of restriction fragment length polymorphisms in two-dimensional separations of human genomic DNAGenomics, 1995
- Immunohistochemical study of cathepsin B. Prognostic significance in human lung cancerCancer, 1994
- Multicolor FISH Mapping of YAC Clones in 3p14 and Identification of a YAC Spanning both FRA3B and the t(3;8) Associated with Hereditary Renal Cell CarcinomaGenomics, 1994
- Expression of the Glucocorticoid Receptor and K-rasGenes in Urethan-Induced Mouse Lung Tumors and Transformed Cell LinesExperimental Lung Research, 1991
- Human Lipoprotein Lipase Complementary DNA SequenceScience, 1987
- Barrett's EsophagusNew England Journal of Medicine, 1986