5-氨基乙酰丙酸标记口腔鳞状细胞癌的荧光分析

Masaru Uekusa
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引用次数: 0

摘要

光动力诊断(PDD)是一种基于在恶性细胞中积累的外源性光激活化合物的管理,然后进行适当的光照射的癌症检测形式。其中5-氨基乙酰丙酸(5-ALA)是光敏剂原卟啉IX (PpIX)的前药。本文描述了5- ala在人口腔癌细胞系中产生PpIX荧光的光谱研究。将5株人口腔鳞癌细胞株移植到scid小鼠体内,采用苏木精-伊红染色法评价肿瘤分化程度。两个、一个和两个细胞系分别为低分化、中等分化和良好分化。在细胞培养条件下,高分化和中等分化的癌细胞免疫组化AE1/AE3的阳性染色率高于低分化的癌细胞。用加或不加甲磺酸去铁胺(DFO)的Dulbecco's Modified Eagle's Medium (DMEM)培养5株细胞系,测定5- ala诱导的PpIX荧光强度。在所有细胞系中,DFO存在时5- ala产生的荧光强度最大。荧光强度随肿瘤分化程度的变化顺序为:低分化、中分化、高分化。提示口腔癌细胞的荧光强度随肿瘤分化程度的不同而不同。然而,即使是分化良好的癌细胞,由于PpIX的细胞积累增加,DFO的加入也会增加5-ALA的光动力敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Fluorescence analysis of oral squamous cell carcinoma with 5-aminolevulinic acid labeling].

Photodynamic diagnosis (PDD) is a form of cancer detection based on the administration of an exogenous photoactivated compound that accumulates in malignant cells, followed by appropriate photo-irradiation. 5-aminolevulinic acid (5-ALA), which is one of these compounds, is a prodrug of the photosensitizer protoporphyrin IX (PpIX). This report describes a spectroscopic study of 5-ALA-generated PpIX fluorescence in human oral cancer cell lines. After transplanting five human oral squamous carcinoma cell lines into scid mice, the degree of tumor differentiation was evaluated by hematoxylin-and-eosin staining. Two, one, and two cell lines were poorly, moderately, and well differentiated, respectively. Under cell culture conditions, well and moderately differentiated cancer cells showed higher positive staining rates of AE1/AE3 than poorly differentiated ones in immunohistochemistry. 5-ALA-induced PpIX fluorescence intensities of five cell lines, which were cultured in Dulbecco's Modified Eagle's Medium (DMEM) treated with or without deferoxamine mesylate (DFO), were measured. In all cell lines, the maximum 5-ALA-generated fluorescence intensity was found in the presence of DFO. The fluorescence intensity varied with the degree of tumor differentiation in the following order: poorly differentiated, moderately differentiated, well differentiated. These results suggest that the fluorescence intensity of oral cancer cells differs according to the degree of tumor differentiation. However, even with well differentiated cancer cells, addition of DFO could increase the photodynamic sensitivity of 5-ALA as a result of greater cellular accumulation of PpIX.

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