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[白细胞介素-23通过无翅相关整合位点/β-连环蛋白途径增强人舌鳞状细胞癌的抗凋亡和耐药性]

[Interleukin-23 strengthens the anti-apoptotic and drug resistance of human tongue squamous cell carcinoma through the Wingless-related integration site/β-catenin pathway].

作者信息

Yan Qin, Su Yuting, Zhou Yuepeng, Zhu Haitao, Yang Xihu, Xu Jianhui

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2015 Jun;33(3):249-54. doi: 10.7518/hxkq.2015.03.007.

Abstract

OBJECTIVE

This study aims to detect the expression level of interleukin-23 (IL-23) in tongue squamous cell carcinoma tissues and its relationship with clinical prognosis, as well as explore the anti-apoptotic and drug resistance of the tongue squamous cell line-SCC9 before and after treatment with IL-23.

METHODS

The expression of IL-23 in tumor tissues from 28 tongue cancer patients was analyzed by immunohistochemistry assay. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the mRNA expression of Wingless-related integration site (Wnt)1 and c-myc in SCC9 cells treated with different IL-23 concentrations. After interferencing the β-catenin with small interfering RNA (siRNA), the expression of β-catenin, B-cell lymphoma-2 (Bcl-2), ATP-binding cassette sub-family G member 2 (ABCG2), and permeability-glycoprotein (P-gp) in SCC9 was measured by Western blot analysis. The effect of IL-23 on the apoptotic resistance of SCC9 to cisplatin was examined by methyl thiazolyl tetrazolium test.

RESULTS

The expression of IL-23 in tongue cancer tissues was correlated with lymphatic metastasis, nerve invasion, and the recurrence after therapy (P<0.05). After dealing with IL-23, SCC9 showed the upregulation effect of Bcl-2, ABCG2 and P-gp expressions. IL-23 was closely related to the activation level of the Wnt pathway and significantly strengthened the resistance to cisplatin (P<0.01).

CONCLUSION

IL-23 activates the Wnt pathway in tongue squamous cell carcinoma, thereby enhancing its resistance to apoptosis and drug.

摘要

目的

本研究旨在检测白细胞介素 - 23(IL - 23)在舌鳞状细胞癌组织中的表达水平及其与临床预后的关系,并探讨IL - 23处理前后舌鳞状细胞系SCC9的抗凋亡和耐药性。

方法

采用免疫组织化学分析法分析28例舌癌患者肿瘤组织中IL - 23的表达。运用定量实时聚合酶链反应(qRT - PCR)检测不同浓度IL - 23处理的SCC9细胞中无翅相关整合位点(Wnt)1和c - myc的mRNA表达。用小干扰RNA(siRNA)干扰β - 连环蛋白后,通过蛋白质免疫印迹分析检测SCC9中β - 连环蛋白、B细胞淋巴瘤 - 2(Bcl - 2)、ATP结合盒转运蛋白G亚家族成员2(ABCG2)和通透糖蛋白(P - gp)的表达。通过噻唑蓝比色法检测IL - 23对SCC9顺铂凋亡抗性的影响。

结果

舌癌组织中IL - 23的表达与淋巴转移、神经侵犯及治疗后复发相关(P<0.05)。经IL - 23处理后,SCC9的Bcl - 2、ABCG2和P - gp表达呈现上调作用。IL - 23与Wnt通路的激活水平密切相关,并显著增强对顺铂的抗性(P<0.01)。

结论

IL - 23激活舌鳞状细胞癌中的Wnt通路,从而增强其抗凋亡和耐药性。

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