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1.  Prognostic significance of overexpression of c-Met oncoprotein in cholangiocarcinoma 
British Journal of Cancer  2011;105(1):131-138.
Background:
Cholangiocarcinoma (CC) is a highly malignant carcinoma. We attempted to clarify the prognostic significance of c-Met overexpression and its association with clinicopathological factors in patients with CC.
Patients and methods:
One hundred and eleven patients with intrahepatic CC (IHCC) and 136 patients with extrahepatic CC (EHCC) who had undergone curative surgery were divided immunohistologically into c-Methigh and c-Metlow groups. Clinicopathological factors and outcomes were compared between the groups. c-Met and epidermal growth factor receptor (EGFR) expression was also examined in 10 CC cell lines.
Results:
The positivity of c-Met was 45.0% in IHCC and 68.4% in EHCC; c-Methigh expression was demonstrated in 11.7% of IHCC and 16.2% of EHCC. c-Methigh expression was significantly correlated with the 5-year survival rate for CC overall (P=0.0046) and for IHCC (P=0.0013), histopathological classification in EHCC, and for EGFR overexpression in both IHCC and EHCC. Coexpression and coactivation of c-Met and EGFR were also observed in CC cell lines. Multivariate analysis revealed that c-Methigh expression was an independent predictor of poor overall and disease-free survival in patients with IHCC.
Conclusions:
c-Met overexpression is associated with EGFR expression and is a poor prognostic factor in CC.
doi:10.1038/bjc.2011.199
PMCID: PMC3137414  PMID: 21673683
c-Met; cholangiocarcinoma; immunohistochemistry; prognostic factor; epidermal growth factor receptor
3.  Induction of Graft Acceptance After Dog Kidney or Liver Transplantation 
Transplantation proceedings  1990;22(1):80-82.
We have reported that, a short delayed course of intramuscular FK 506 can induce a,donor strain-specific immunologic unresponsiveness to cardiac allograft in rats.1 Further studies have been performed to determine if this agent can induce graft acceptance after canine renal (KT) or hepatic (OLT) allotransplantation. Preliminary descriptions of these efforts have been published.2
PMCID: PMC3032582  PMID: 1689909

Results 1-25 (49)