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本文引用的文献

1
Ezrin expression in prostate cancer and benign prostatic tissue.埃兹蛋白在前列腺癌和前列腺良性组织中的表达。
Eur Urol. 2005 Nov;48(5):852-7. doi: 10.1016/j.eururo.2005.03.013. Epub 2005 Apr 1.
2
Prognostic impact of immunohistochemical expression of ezrin in highly malignant soft tissue sarcomas.埃兹蛋白免疫组化表达在高度恶性软组织肉瘤中的预后影响
Clin Cancer Res. 2005 Sep 1;11(17):6198-204. doi: 10.1158/1078-0432.CCR-05-0548.
3
The membrane cytoskeletal crosslinker ezrin is required for metastasis of breast carcinoma cells.膜细胞骨架交联蛋白埃兹蛋白是乳腺癌细胞转移所必需的。
Breast Cancer Res. 2005;7(3):R365-73. doi: 10.1186/bcr1006. Epub 2005 Mar 21.
4
Nuclear expression of maspin is associated with a lower recurrence rate and a longer disease-free interval after surgery for squamous cell carcinoma of the larynx.在喉鳞状细胞癌手术后,乳腺丝抑蛋白的核表达与较低的复发率和较长的无病生存期相关。
Histopathology. 2005 May;46(5):576-82. doi: 10.1111/j.1365-2559.2005.02141.x.
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Molecular profiling of tumor progression in head and neck cancer.头颈部癌肿瘤进展的分子剖析
Arch Otolaryngol Head Neck Surg. 2005 Jan;131(1):10-8. doi: 10.1001/archotol.131.1.10.
6
Src-dependent ezrin phosphorylation in adhesion-mediated signaling.黏附介导信号传导中Src依赖的埃兹蛋白磷酸化
Mol Biol Cell. 2005 Mar;16(3):1481-90. doi: 10.1091/mbc.e04-08-0721. Epub 2005 Jan 12.
7
Ezrin in primary cutaneous melanoma.原发性皮肤黑色素瘤中的埃兹蛋白
Mod Pathol. 2005 Apr;18(4):503-10. doi: 10.1038/modpathol.3800300.
8
Prognostic significance of nm23-H1 expression in esophageal squamous cell carcinoma.nm23-H1在食管鳞状细胞癌中的预后意义
Eur J Cardiothorac Surg. 2004 Aug;26(2):419-24. doi: 10.1016/j.ejcts.2004.03.045.
9
Prognostic significance of nm23-H1 expression in oral squamous cell carcinoma.nm23-H1表达在口腔鳞状细胞癌中的预后意义
Br J Cancer. 2004 Jun 1;90(11):2186-93. doi: 10.1038/sj.bjc.6601808.
10
Expression of ezrin in prostatic intraepithelial neoplasia.埃兹蛋白在前列腺上皮内瘤变中的表达。
Urology. 2004 Mar;63(3):609-12. doi: 10.1016/j.urology.2003.09.068.

埃兹蛋白、乳腺丝抑蛋白和nm23-H1蛋白表达在预测接受根治性放疗的头颈部鳞状细胞癌患者预后中的价值。

Value of ezrin, maspin and nm23-H1 protein expressions in predicting outcome of patients with head and neck squamous-cell carcinoma treated with radical radiotherapy.

作者信息

Mhawech-Fauceglia Paulette, Dulguerov Pavel, Beck Amy, Bonet Marta, Allal Abdelkarim S

机构信息

Department of Pathology, Geneva University Hospital, Geneva, Switzerland.

出版信息

J Clin Pathol. 2007 Feb;60(2):185-9. doi: 10.1136/jcp.2006.036624. Epub 2006 May 12.

DOI:10.1136/jcp.2006.036624
PMID:16698950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1860631/
Abstract

BACKGROUND

Prognostic factors in predicting outcomes in patients with head and neck squamous-cell carcinoma (HNSCC) are limited to the clinical-pathological parameters, including lymph node metastasis, location, grade and stage of the disease.

AIM

To determine whether the expression of these proteins has a value in predicting patient outcome.

METHODS

Ezrin, maspin and nm23-H1 immunohistochemistry in tissue samples of 120 patients with HNSCC were evaluated using the microarray technique.

RESULTS

In determining the association among each of the three proteins and the clinical-pathological parameters, low maspin expression was the only one found to be significantly associated with high tumour grade (p = 0.007); all others showed no significant associations. In univariate analysis, patients with tumours expressing high ezrin had a shorter disease-free survival (DFS) of 51% than those with low ezrin expression (DFS 84%; p = 0.08). In multivariate analysis, tumours with the combination of loss of maspin and low histological grade had longer DFS (83%) compared with those with high maspin and high histological grade (DFS 42%; p = 0.08).

CONCLUSION

Our study is the first to determine the value of ezrin and maspin in HNSCC in a large series of patients with long follow-up. Ezrin and maspin seem to have a potential prognostic value in patients with HNSCC but results should be confirmed with further studies.

摘要

背景

预测头颈部鳞状细胞癌(HNSCC)患者预后的因素仅限于临床病理参数,包括淋巴结转移、疾病部位、分级和分期。

目的

确定这些蛋白的表达在预测患者预后方面是否具有价值。

方法

采用微阵列技术评估120例HNSCC患者组织样本中的埃兹蛋白、组织蛋白酶抑制因子和nm23-H1免疫组化情况。

结果

在确定这三种蛋白各自与临床病理参数之间的关联时,发现组织蛋白酶抑制因子低表达是唯一与高肿瘤分级显著相关的因素(p = 0.007);其他均无显著关联。单因素分析显示,埃兹蛋白高表达的肿瘤患者无病生存期(DFS)为51%,低于埃兹蛋白低表达患者(DFS 84%;p = 0.08)。多因素分析显示,组织蛋白酶抑制因子缺失与低组织学分级组合的肿瘤患者DFS较长(83%),而组织蛋白酶抑制因子高表达与高组织学分级组合的患者DFS为42%(p = 0.08)。

结论

我们的研究首次在大量长期随访的患者中确定了埃兹蛋白和组织蛋白酶抑制因子在HNSCC中的价值。埃兹蛋白和组织蛋白酶抑制因子似乎在HNSCC患者中具有潜在的预后价值,但结果应通过进一步研究加以证实。