| Project/Area Number |
07671997
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Morphological basic dentistry
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| Research Institution | Asahi University |
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Principal Investigator |
TAKAI Yoshiaki Asahi University, School of Dentistry Professor, 歯学部, 教授 (70197044)
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| Co-Investigator(Kenkyū-buntansha) |
YAMADA Kazuo Asahi University, School of Dentistry Assistant, 歯学部, 助手 (50240007)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1996: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1995: ¥1,200,000 (Direct Cost: ¥1,200,000)
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| Keywords | Pleomorphic adenoma / myoepithelioma / neoplastic myoepithelial cell / myoepithelial cell / salivary gland / muscle-specific actin / cytokeratin / myofilament / muscle specific actin / 免疫組織化学 |
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| Research Abstract |
Determining criteria for identifying neoplastic myoepithlium is criticalfor proper classification of salivary gland tumors. Muscle-specific actin (MSA) and intermediate filament expression were determined in methanol-fixed pleomorphic adenomas (PA ; n=14) and myoepithliomas (MYO ; N=5), as well as myofilament formation in electron micrographs of 22 PA and 10 MYO.
Immunoelectron microscopy (IEM) for MSA was performed on 6 PA and 2 MYO.Considerably less MSA and cytokeratin 14 (CK14), two markers for normal myoepithlial cells, were detected in nonluminal cells of PA and tumor cells MY than expected ; only 5/14 PA (36%) and 2/5 MYO (40%) had significant numbers (ranging from 5-80%) of positive tumor cells. Expression of CK14 was also limited (50% of PA and 40% of MYO with 10-70% and 10-40% cells positive, respectively). Vimentin was strongly and diffusely (90-100% of cells) expressed in all PA and MYO,while GFAP was noted in 93% of PA (25-100% cells positive) and 100% of MYO (10-60% cells positive).
By routine EM,only one-third of PA and MYO had small numbers of tumor cells with myofilaments (in only one MYO were these moderately prominent), while IEM (n=8) revealed MSA-colloidal gold positive myofilaments in 2 PA and 1 MYO,all of which appeared to lack myofilaments by routine EM.
Clearly, the lack of myofilament detection by immunohistochemistry or EM does not exclude a diagnosis of PA or MYO when growth patterns and cell type indicate such a diagnosis ; this even applies to plasmacytoid MYO.IEM shows muscle-actin can be detected even when myofilaments are apparently absent or minimal by routine EM.Vimentin and GFAP are more consistent markers for neoplastic myoepithelial cells than actin and CK14.
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