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局麻药对人口腔正常细胞和肿瘤细胞的细胞毒性及细胞死亡类型的影响。

Cytotoxicity and type of cell death induced by local anesthetics in human oral normal and tumor cells.

机构信息

Division of Anesthesiology, Meikai University School of Dentistry, Sakado, Saitama 350-0283, Japan.

出版信息

Anticancer Res. 2012 Jul;32(7):2925-33.

Abstract

BACKGROUND

Local anesthetics are often administered to tumors and surrounding tissues during the surgery of the head and neck area, however their effects on oral tissues is not well understood. In the present study, the cytotoxicity of a total of seven local anesthetics towards oral tumor and normal cells was compared.

MATERIALS AND METHODS

Tumor-specificity index was determined by the ratio of the mean 50% cytotoxic concentration against normal cells to that for tumor cells. Apoptosis induction was monitored by internucleosomal DNA fragmentation and caspase-3, -8, and - 9 activation. Fine cell structure was observed under transmission electron microscopy.

RESULTS

All local anesthetics showed slightly higher cytotoxicity towards oral squamous cell carcinoma (OSCC) cell lines than towards normal oral cells. Dibucaine, with a log p-value of approximately 3, was the most cytotoxic, followed by tetracaine, bupivacaine or ethylaminobenzoate, whereas lidocaine, procaine and mepivacain were much less cytotoxic. When the tumor-specificity was evaluated between OSCC and human skin keratinocytes, the index was 6.6. Dibucaine did not induce apoptosis of OSCC cells. On the other hand, dibucaine did induce mitochondrial injury and swelling, formation of secondary lysosomes, and at high concentrations, rupture of the cell membrane. Autophagy inhibitors did not reduce the cytotoxicity of dibucaine.

CONCLUSION

Necrosis may be involved in the induction of antitumor activity by dibucaine.

摘要

背景

在头颈部区域的手术中,常将局部麻醉剂施用于肿瘤及周围组织,但它们对口腔组织的作用尚未完全了解。本研究比较了七种局部麻醉剂对口腔肿瘤和正常细胞的细胞毒性。

材料和方法

通过正常细胞与肿瘤细胞的平均 50%细胞毒性浓度比来确定肿瘤特异性指数。通过核小体间 DNA 片段化和 caspase-3、-8、-9 的激活来监测细胞凋亡的诱导。采用透射电子显微镜观察细胞精细结构。

结果

所有局部麻醉剂对口腔鳞状细胞癌(OSCC)细胞系的细胞毒性均略高于对正常口腔细胞的毒性。具有约 3 的 log p 值的丁卡因最具细胞毒性,其次是地卡因、布比卡因或乙基氨基苯甲酸酯,而利多卡因、普鲁卡因和甲哌卡因的细胞毒性则小得多。当在 OSCC 和人皮肤角质形成细胞之间评估肿瘤特异性时,指数为 6.6。丁卡因不会诱导 OSCC 细胞凋亡。另一方面,丁卡因确实会诱导线粒体损伤和肿胀、次级溶酶体的形成,并且在高浓度下会导致细胞膜破裂。自噬抑制剂并不能降低丁卡因的细胞毒性。

结论

坏死可能参与了丁卡因的抗肿瘤活性诱导。

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