Expression of autocrine motility factor mRNA is a poor prognostic factor in high‐grade astrocytoma

Y Tanizaki, Y Sato, H Oka, S Utsuki… - Pathology …, 2006 - Wiley Online Library
Y Tanizaki, Y Sato, H Oka, S Utsuki, K Kondo, Y Miyajima, R Nagashio, K Fujii
Pathology international, 2006Wiley Online Library
It has been reported that tumor infiltration is correlated with the expression of autocrine
motility factor (AMF) and its receptor 78 kDa glycoprotein (gp78). The purpose of the present
study was to detect AMF and gp78 mRNA expression levels and their localization in high‐
grade astrocytomas (glioblastoma and anaplastic astrocytoma) and to determine whether
AMF and gp78 are important prognostic factors. A total of 32 formalin‐fixed and paraffin‐
embedded glioblastomas and 23 formalin‐fixed and paraffin‐embedded anaplastic …
It has been reported that tumor infiltration is correlated with the expression of autocrine motility factor (AMF) and its receptor 78 kDa glycoprotein (gp78). The purpose of the present study was to detect AMF and gp78 mRNA expression levels and their localization in high‐grade astrocytomas (glioblastoma and anaplastic astrocytoma) and to determine whether AMF and gp78 are important prognostic factors. A total of 32 formalin‐fixed and paraffin‐embedded glioblastomas and 23 formalin‐fixed and paraffin‐embedded anaplastic astrocytomas was used. The expressions of AMF and gp78 mRNA were detected using the highly sensitive in situ hybridization method. The expression of AMF mRNA was detected in 27 of 32 glioblastomas (84.4%) and 11 of 23 anaplastic astrocytomas (47.8%). The positivity of AMF mRNA was significantly higher in glioblastomas than in anaplastic astrocytomas (P = 0.0094), but gp78 mRNA was detected in most cases and no statistical significance was observed. The overall survival of patients with AMF expression was significantly shorter than patients without AMF expression (P = 0.0175). In anaplastic astrocytomas, the overall survival of patients with AMF expression was also significantly shorter than in patients without AMF expression (P = 0.0058). This study demonstrated that AMF is a poor prognostic factor in high‐grade astrocytomas.
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