Expression and Prognostic Value of Oct-4 in Astrocytic Brain TumorsReport as inadecuate




Expression and Prognostic Value of Oct-4 in Astrocytic Brain Tumors - Download this document for free, or read online. Document in PDF available to download.

Background

Glioblastomas are the most frequent type of malignant primary brain tumor with a median overall survival less than 15 months. Therapy resistance of glioblastomas has been attributed to the presence of tumor initiating stem-like cells TSCs. TSC-related markers have therefore been suggested to have promising potentials as prognostic markers in gliomas.

Methodology-Principal Findings

The aim of the present study was to investigate the expression and prognostic impact of the TSC-related marker Oct-4 in astrocytic brain tumors of increasing grade. In total 114 grade II, III and IV astrocytic brain tumors were immunohistochemically stained for Oct-4, and the fraction and intensity of Oct-4 positive cells were determined by morphometric analysis of full tumor sections. Oct-4 was expressed in all tumors, and the Oct-4 positive cell fraction increased with tumor grade p = 0.045. There was no association between survival and Oct-4 positive cell fraction, neither when combining all tumor grades nor in analysis of individual grades. Oct-4 intensity was not associated with grade, but taking IDH1 status into account we found a tendency for high Oct-4 intensity to be associated with poor prognosis in anaplastic astrocytomas. Double immunofluorescence stainings showed co-localization in the perivascular niches of Oct-4 and two other TSC markers CD133 and nestin in glioblastomas. In some areas Oct-4 was expressed independently of CD133 and nestin.

Conclusions

In conclusion, high Oct-4 fraction was associated with tumor malignancy, but seemed to be without independent prognostic influence in glioblastomas. Identification of a potential prognostic value in anaplastic astrocytomas requires additional studies using larger patient cohorts.



Author: Jeanette Krogh Petersen , Per Jensen , Mia Dahl Sørensen, Bjarne Winther Kristensen

Source: http://plos.srce.hr/



DOWNLOAD PDF




Related documents