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High FABP5 versus CRABPII expression ratio in recurrent craniopharyngiomas: Implications for future treatment
Abstract Background and objective Recurrence is a major problem in craniopharyngioma (CP) management. Recent study shows that high FABP5/CRABPII may be related to tumor growth and Al-trans retinoic acid (ATRA) may suppress primary CP growth. We intended to study the expression profile of FABP5 and C...
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Published in: | World neurosurgery 2016-10, Vol.94, p.197-205 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract Background and objective Recurrence is a major problem in craniopharyngioma (CP) management. Recent study shows that high FABP5/CRABPII may be related to tumor growth and Al-trans retinoic acid (ATRA) may suppress primary CP growth. We intended to study the expression profile of FABP5 and CRABPII in recurrent CP tissue and the effect of ATRA on recurrent CP cells. Methods Fifty cases of CP patients were enrolled in the retrospective study. Among them, 15 were recurrent. Fresh specimens were collected for immunohistochemistry (IHC), RT-PCR and Western-blotting analysis of FABP5 and CRABPII. Fresh specimens from 6 primary and recurrent CPs were collected and subjected to cell culture using explants method. ATRA at various concentrations was applied to recurrent CP cell culture, and cell growth were recorded and analyzed. Results IHC, RT-PCR and Western-blot study showed that FABP5 was expressed significantly higher in recurrent tumors , while CRABPII in primary ones. FABP5/CRABPII ratio was significantly higher in recurrent rather than primary tumors. Recurrent CP cell grew faster than primary cells, and ATRA induced cellular apoptosis and inhibited CP cell growth in dose dependent manner. Conclusions High expression ratio between FABP5 and CRABPII may be related to CP tumor recurrence and ATRA could be a potential therapeutic agent for CP chemotherapy. |
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ISSN: | 1878-8750 1878-8769 |
DOI: | 10.1016/j.wneu.2016.05.063 |