傅里叶变换红外光谱测定口腔粘膜鳞状细胞癌与正常口腔粘膜差异的研究

Yoshikuni Fukuyama, Satoshi Yoshida, Shigetaka Yanagisawa, Masatsugu Shimizu
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引用次数: 70

摘要

我们研究了口腔鳞状细胞癌(OSCC)与正常牙龈上皮(NGE)或正常牙龈下组织(NST)的傅里叶变换红外光谱(FTIR)的差异。我们使用了15例未经测量前处理的OSCC和10例NGE或NST。我们还使用了培养的口腔鳞状细胞癌(COSCC)和移植到大鼠下背部3个月后聚集的组织(MSCC)。这些组织光谱与纯化的人胶原蛋白和人角蛋白进行比较。每个组织标本的一半用FTIR测量,另一半进行组织学研究。在1431 ~ 1482 cm−1波段和1183 ~ 1274 cm−1波段,OSCC和NGE的FTIR光谱存在差异。1368 cm−1处的肩峰在OSCC中趋于消失,NGE中1246和1083 cm−1处的峰分别趋向于向OSCC中1242和1086 cm−1处的峰转移。发现NST的红外光谱受到胶原蛋白存在的强烈影响。OSCC和NGE的二阶导数FTIR光谱也有显著差异。我们的数据表明,该红外技术适用于临床诊断。©1999 John Wiley &儿子,Inc。生物光谱学学报(英文版),1999
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A study on the differences between oral squamous cell carcinomas and normal oral mucosas measured by Fourier transform infrared spectroscopy

We investigated the differences of Fourier transform infrared (FTIR) spectra between oral squamous cell carcinoma (OSCC) and normal gingival epithelium (NGE) or normal subgingival tissue (NST). We used 15 specimens of OSCC which had not been treated before measurement and 10 of NGE or NST. We also used cultured oral squamous cell carcinoma (COSCC) and the tissue (MSCC) which massed for 3 months after the cultured oral squamous cell carcinoma was transplanted into the lower back of a rat. Those tissue spectra were compared with the purified human collagens and human keratin. One half of every tissue specimen was measured with FTIR and the other half was investigated histologically. The differences of FTIR spectra between OSCC and NGE were observed in the bands between 1431 and 1482 cm−1 and between 1183 and 1274 cm−1. The shoulder at 1368 cm−1 tended to disappear in OSCC, and the peaks at 1246 and 1083 cm−1 found in NGE tended to shift to those at 1242 and 1086 cm−1 in OSCC, respectively. The infrared spectrum of NST was noticed to be strongly influenced by the presence of collagen. Significant differences were also observed in the second derivative FTIR spectra between OSCC and NGE. Our data suggested that this infrared technique is applicable to clinical diagnostics. © 1999 John Wiley & Sons, Inc. Biospectroscopy 5: 117–126, 1999

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