bFGF induces differentiation and death of olfactory neuroblastoma cells

被引:15
作者
Nibu, K
Li, GQ
Kaga, K
Rothstein, JL
机构
[1] Thomas Jefferson Univ, Jefferson Med Coll, Kimmel Canc Inst, Dept Otolaryngol Head & Neck Surg, Philadelphia, PA 19107 USA
[2] Univ Tokyo, Fac Med, Dept Otolaryngol Head & Neck Surg, Tokyo 113, Japan
关键词
AML1; basic fibroblast growth factor; BDNF; esthesioneuroblastoma; Ewing's sarcoma; EWS/Fli-1; FGFR-1; NGFR; athymic mice; olfactory neuroblastoma; pPNET; Trk;
D O I
10.1006/bbrc.2000.3899
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Olfactory neuroblastoma (ONB) is a highly vascularized and malignant tumor arising in olfactory neuronal, precursors from the paranasal sinuses. Previously, we showed that treatment of JFEN cells with transforming growth factor (TGF)-alpha caused them to differentiate and respond to chemical odorants, whereas basic fibroblast growth factor (bFGF) treated cells differentiated and died. In the present study we show that established ONE tumors treated with bFGF upregulate the bFGF receptor (FGFR1) prior to differentiation. This cellular differentiation was evidenced by bFGF-induced expression of the human runt homologue AML1 (PEBP2 alphaB, CBFA-2) that is highly expressed in developing olfactory neuroepithelium and TrkA, a preferred nerve growth factor receptor. Since TrkA is expressed in supporting cells, but not in mature olfactory neurons, we hypothesize that the expression of AML1 and TrkA in bFGF-treated JFEN cells induced supporting cell differentiation. Collectively, these results have implications for the treatment of patients afflicted with ONE. (C) 2000 Academic Press.
引用
收藏
页码:172 / 180
页数:9
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