PMID- 11355950 OWN - NLM STAT- MEDLINE DCOM- 20010628 LR - 20220419 IS - 0007-0920 (Print) IS - 1532-1827 (Electronic) IS - 0007-0920 (Linking) VI - 84 IP - 10 DP - 2001 May 18 TI - Expression and clinical significance of erb-B receptor family in hepatocellular carcinoma. PG - 1377-83 AB - In order to elucidate the clinical significance of the erbB family, epidermal growth factor receptor (EGF-R), c-erbB-2, c-erbB-3 and c-erbB-4 in hepatocellular carcinoma (HCC), we investigated the expression of these proteins by means of immunohistochemistry for HCC as well as adjacent noncancerous lesions. EGF-R was expressed in 68% of the HCC examined and showed correlation with the proliferating activity, stage, intrahepatic metastasis and carcinoma differentiation. c-erbB-2 was expressed in only 21% of the cases and showed no relationships with the clinicopathological parameters. c-erbB-3 protein was observed in 84% of the HCC and 38.1% of the noncancerous lesions. Its expression in HCC was equal to or greater than noncancerous lesions in 90.5% of the cases, and was related to the stage, portal invasion, cell proliferating activity, tumour size, intrahepatic metastasis and carcinoma differentiation. c-erbB-4 protein was expressed in 61.0% of HCC and in as much as 86.1% of the noncancerous lesions. Unlike the expression of c-erbB-3, that of c-erbB-4 in HCC was less than that of the adjacent noncancerous lesions in 51.2% of the cases. No statistical significance could be established between this protein expression in HCC and clinicopathological features. EGF-R and c-erbB-3 affected disease-free survival, but were not recognized as independent prognostic factors by multivariate analysis. The present study suggests that, of the four receptors, EGF-R and c-erbB-3 play important roles in the progression of HCC. CI - Copyright 2001 Cancer Research Campaign. FAU - Ito, Y AU - Ito Y AD - Department of Surgery, Osaka Seamen's Insurance Hospital, 1-8-30, Chikko, Minato-ku, Osaka, 552-0021, Japan. FAU - Takeda, T AU - Takeda T FAU - Sakon, M AU - Sakon M FAU - Tsujimoto, M AU - Tsujimoto M FAU - Higashiyama, S AU - Higashiyama S FAU - Noda, K AU - Noda K FAU - Miyoshi, E AU - Miyoshi E FAU - Monden, M AU - Monden M FAU - Matsuura, N AU - Matsuura N LA - eng PT - Journal Article PL - England TA - Br J Cancer JT - British journal of cancer JID - 0370635 RN - EC 2.7.10.1 (ERBB4 protein, human) RN - EC 2.7.10.1 (ErbB Receptors) RN - EC 2.7.10.1 (Receptor, ErbB-2) RN - EC 2.7.10.1 (Receptor, ErbB-3) RN - EC 2.7.10.1 (Receptor, ErbB-4) SB - IM MH - Carcinoma, Hepatocellular/*pathology/surgery MH - Disease-Free Survival MH - ErbB Receptors/*analysis MH - Female MH - Follow-Up Studies MH - Humans MH - Immunohistochemistry MH - Liver/pathology MH - Liver Neoplasms/*pathology/surgery MH - Male MH - Middle Aged MH - Neoplasm Invasiveness MH - Neoplasm Metastasis MH - Receptor, ErbB-2/*analysis MH - Receptor, ErbB-3/*analysis MH - Receptor, ErbB-4 MH - Retrospective Studies MH - Time Factors PMC - PMC2363640 EDAT- 2001/05/18 10:00 MHDA- 2001/06/29 10:01 CRDT- 2001/05/18 10:00 PHST- 2001/05/18 10:00 [pubmed] PHST- 2001/06/29 10:01 [medline] PHST- 2001/05/18 10:00 [entrez] AID - S0007092000915805 [pii] AID - 10.1054/bjoc.2000.1580 [doi] PST - ppublish SO - Br J Cancer. 2001 May 18;84(10):1377-83. doi: 10.1054/bjoc.2000.1580.