组织蛋白酶B、H、L、D及其内源性抑制剂stefins A和B在头颈部癌中的预后价值。

M Budihna, P Strojan, L Smid, J Skrk, I Vrhovec, A Zupevc, Z Rudolf, M Zargi, M Krasovec, B Svetic, N Kopitar-Jerala, J Kos
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引用次数: 75

摘要

为了评估组织蛋白酶B、H、L、D和stefins A、B在头颈部癌中的预后价值,我们测量了它们在原发性肿瘤和邻近正常组织的细胞质中的浓度(45例患者中组织蛋白酶B、D stefins A、B, 24例患者中组织蛋白酶L, 21例患者中组织蛋白酶H)。肿瘤组织蛋白酶B、L和D的中位浓度显著高于邻近正常组织(B和D: p < 0.0001;L: p = 0.004);正常组织中组织蛋白酶H浓度较高(p = 0.001)。两种stefin的浓度在正常组织和肿瘤组织之间没有显著差异。组织蛋白酶B、H、L和D在喉部组织中的浓度高于非喉部正常组织和肿瘤组织。组织蛋白酶B在肿瘤组织中差异有统计学意义(p = 0.045),在正常组织中差异有统计学意义(p = 0.07)。早期肿瘤中stefins A和B的浓度低于局部晚期肿瘤(stefins A: p = 0.04;stefin B: p = 0.07)。肿瘤组织中组织蛋白酶L浓度低于或等于临界值的患者无病生存率和疾病特异性生存率更高(p = 0.035;p = 0.05),而组织蛋白酶B仅在无病生存中存在差异(p = 0.07)。stefin A的情况正好相反(p = 0.0002;p = 0.002)和stefin B (p = 0.009;p = 0.003),组织蛋白酶H对无病生存率也有影响(p = 0.055)。组织蛋白酶D的浓度与存活率无相关性。我们的数据表明,组织蛋白酶B、H、L和ste蛋白酶A和B在头颈部癌中可能具有预后价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic value of cathepsins B, H, L, D and their endogenous inhibitors stefins A and B in head and neck carcinoma.

To estimate the prognostic value of cathepsins B, H, L, D and stefins A and B in head and neck carcinoma, their concentrations in cytosols of primary tumours and adjacent normal tissue were measured (cathepsins B, D stefins A, B in 45, cathepsin L in 24 and cathepsin H in 21 patients). Median concentrations of cathepsins B, L, and D were significantly higher in tumour than in the adjacent normal tissue (B and D: p < 0.0001; L: p = 0.004); cathepsin H concentration was higher in normal tissue (p = 0.001). Concentrations of either stefin did not differ significantly between normal and tumour tissue. Concentrations of cathepsins B, H, L, and D were higher in laryngeal than in non-laryngeal normal and tumour tissues. The difference was statistically significant for cathepsin B in tumour tissue (p = 0.045), and marginally significant in normal tissue (p = 0.07). Early tumours had lower concentrations of stefins A and B than locally advanced tumours (stefin A: p = 0.04; stefin B: p = 0.07). Disease-free and disease-specific survival rates were better in patients with concentrations of cathepsin L in tumour tissue below or equal to the cut-off values (p = 0.035; p = 0.05), whereas for cathepsin B the difference was established only for disease-free survival (p = 0.07). The opposite was true for stefin A (p = 0.0002; p = 0.002) and stefin B (p = 0.009; p = 0.003), and in disease-free survival also for cathepsin H (p = 0.055). The concentration of cathepsin D did not correlate with survival. Our data indicate that cathepsins B, H, L and stefins A and B might have prognostic value in head and neck carcinoma.

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