2017
DOI: 10.18632/oncotarget.20815
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Combination immunohistochemistry for SMAD4 and Runt-related transcription factor 3 may identify a favorable prognostic subgroup of pancreatic ductal adenocarcinomas

Abstract: PurposesSMAD4/DPC4 mutations have been associated with aggressive behavior in pancreatic ductal adenocarcinomas (PDAC), and it has recently been suggested that RUNX3 expression combined with SMAD4 status may predict the metastatic potential of PDACs. We evaluated the prognostic utility of SMAD4/RUNX3 status in human PDACs by immunohistochemistry.Materials and MethodsImmunohistochemical stains were performed for SMAD4 and RUNX3 on 210 surgically resected PDACs, and the results were correlated with the clinicopa… Show more

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Cited by 3 publications
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“…Su et al reported that TF 7 served as a poor prognostic marker of glioblastoma multiforme by enhancing proliferation by upregulating c-myc [9]. Lee et al suggested that combination immunohistochemistry for SMAD4 and runt-related TF 3 may determine a favorable prognostic subgroup of pancreatic ductal adenocarcinomas [10]. Fan et al reported that microRNA-301a-3p overexpression may contribute to cell invasion and proliferation by targeting runtrelated TF 3 in prostate cancer [11].…”
mentioning
confidence: 99%
“…Su et al reported that TF 7 served as a poor prognostic marker of glioblastoma multiforme by enhancing proliferation by upregulating c-myc [9]. Lee et al suggested that combination immunohistochemistry for SMAD4 and runt-related TF 3 may determine a favorable prognostic subgroup of pancreatic ductal adenocarcinomas [10]. Fan et al reported that microRNA-301a-3p overexpression may contribute to cell invasion and proliferation by targeting runtrelated TF 3 in prostate cancer [11].…”
mentioning
confidence: 99%