Assessment of muscarinic and nicotinic acetylcholine receptor expression in primitive neuroectodermal tumor/Ewing family of tumor and desmoplastic small round cell tumor: An immunohistochemical and Western blot study of tissue microarray and cell lines

被引:11
|
作者
Schlauder, Scott M. [2 ]
Steffensen, Thora S. [2 ]
Morgan, Michael [3 ]
Letson, Douglas G. [4 ]
Pledger, Warren J. [5 ]
Ma, Le [5 ]
Bui, Marilyn M. [1 ,4 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Div Anat Pathol, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Anat Cell Biol & Pathol, Tampa, FL USA
[3] James Hailey VA Hosp, Dept Pathol, Tampa, FL USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Sarcoma Program, Tampa, FL 33612 USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Mol Oncol Program, Tampa, FL 33612 USA
关键词
acetylcholine receptor; immunohistochemistry; tissue microarray; Ewing sarcoma; primitive neuroectodermal tumor; sarcoma; Western blot;
D O I
10.1080/15513810802077529
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The primitive neuroectodermal tumor (PNET)/Ewing family of tumors (EFT) and desmoplastic small round cell tumor (DSRCT) portend a grave prognosis. Ongoing research in similar neurocrest-derived neoplasms has implicated both the muscarinic acetylcholine receptor (mAChR) and nicotinic acetylcholine receptor (nAChR) in the pathogenesis of these neoplasms. Acetylcholine has been reported to impart a modulatory effect on chemotaxis and proliferation, an effect ameliorated by anticholinergic drugs. The aim of our study is to characterize the pattern of expression of mAChR and nAChR in PNET/EFT and DSRCT, in hopes of discovering a potential target for therapeutic improvements. We examined 34 cases of PNET/EFT and 2 DSRCT retrospectively by immunohistochemical studies. We found that AChRs are overexpressed in a significant number of PNET/EFT and DSRCT. The Western blot analysis of 3 human Ewing sarcoma cell lines confirms the presence of AChRs. Future studies are planned to confirm these results as well as to investigate their potential therapeutic implications.
引用
收藏
页码:83 / 97
页数:15
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