PMID- 12044528 OWN - NLM STAT- MEDLINE DCOM- 20021210 LR - 20211203 IS - 0168-8278 (Print) IS - 0168-8278 (Linking) VI - 36 IP - 6 DP - 2002 Jun TI - Gene amplification and mRNA and protein overexpression of c-erbB-2 (HER-2/neu) in human intrahepatic cholangiocarcinoma as detected by fluorescence in situ hybridization, in situ hybridization, and immunohistochemistry. PG - 780-5 AB - BACKGROUND/AIMS: The human proto-oncogene c-erbB-2 (also called HER-2/neu) is located on chromosome 17q21-22. There have been no studies on gene amplification or mRNA expression of c-erbB-2 in human intrahepatic cholangiocarcinoma (CC) hitherto. METHODS: We investigated c-erbB-2 gene amplification by fluorescence in situ hybridization (FISH), c-erbB2 mRNA expression by ISH, and c-erbB-2 protein expression by immunohistochemistry in 22 archival cases of CC. RESULTS: FISH revealed that c-erbB-2 gene signals were increased in CC. ISH showed that c-erbB-2 mRNA signals were located in the nuclei and cytoplasms of cancer cells and were increased in cancer cells compared with non-cancerous bile ducts where no signals were present. Immunohistochemistry showed that the c-erbB-2 protein was expressed in the cell membrane of cancer cells, and was increased compared with non-cancerous bile ducts where no expression was found. There was a positive significant correlation between c-erbB-2 mRNA and protein expression. Clinicopathologically, there were no correlations between the c-erbB-2 expression and various pathological features. CONCLUSIONS: These data suggest that c-erbB-2 gene amplification does occur in CC, and that there is an overexpressed c-erbB-2 protein through the enhanced mRNA expression. The c-erbB-2 gene amplification may be related to the oncogenesis or tumor progression of CC. FAU - Ukita, Yoko AU - Ukita Y AD - Second Department of Pathology, Tottori University Faculty of Medicine, 86 Nishi-cho, Yonago 683-8503, Japan. FAU - Kato, Masako AU - Kato M FAU - Terada, Tadashi AU - Terada T LA - eng PT - Journal Article PL - Netherlands TA - J Hepatol JT - Journal of hepatology JID - 8503886 RN - 0 (MAS1 protein, human) RN - 0 (Proto-Oncogene Mas) RN - 0 (RNA, Messenger) RN - EC 2.7.10.1 (Receptor, ErbB-2) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Cholangiocarcinoma/chemistry/*physiopathology MH - Female MH - Gene Amplification MH - Gene Expression Regulation, Neoplastic MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization MH - In Situ Hybridization, Fluorescence MH - Liver Neoplasms/chemistry/*physiopathology MH - Male MH - Middle Aged MH - Proto-Oncogene Mas MH - RNA, Messenger/analysis MH - Receptor, ErbB-2/analysis/*genetics EDAT- 2002/06/05 10:00 MHDA- 2002/12/11 04:00 CRDT- 2002/06/05 10:00 PHST- 2002/06/05 10:00 [pubmed] PHST- 2002/12/11 04:00 [medline] PHST- 2002/06/05 10:00 [entrez] AID - S0168827802000570 [pii] AID - 10.1016/s0168-8278(02)00057-0 [doi] PST - ppublish SO - J Hepatol. 2002 Jun;36(6):780-5. doi: 10.1016/s0168-8278(02)00057-0.