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本文引用的文献

1
Matrix metalloproteinases and their clinical relevance in urinary bladder cancer.基质金属蛋白酶及其在膀胱癌中的临床相关性。
Nat Rev Urol. 2011 May;8(5):241-54. doi: 10.1038/nrurol.2011.44. Epub 2011 Apr 12.
2
Roles of matrix metalloproteinases in cancer progression and their pharmacological targeting.基质金属蛋白酶在癌症进展中的作用及其药理学靶向。
FEBS J. 2011 Jan;278(1):16-27. doi: 10.1111/j.1742-4658.2010.07919.x. Epub 2010 Nov 19.
3
Matrix metalloproteinase-2 and matrix metalloproteinase-9 codistribute with transcription factors RUNX1/AML1 and ETV5/ERM at the invasive front of endometrial and ovarian carcinoma.基质金属蛋白酶-2 和基质金属蛋白酶-9 与转录因子 RUNX1/AML1 和 ETV5/ERM 一起分布在子宫内膜癌和卵巢癌的浸润前沿。
Hum Pathol. 2011 Jan;42(1):57-67. doi: 10.1016/j.humpath.2010.01.025. Epub 2010 Oct 20.
4
Tissue inhibitor of metalloproteinase-2 regulates matrix metalloproteinase-2-mediated endothelial barrier dysfunction and breast cancer cell transmigration through lung microvascular endothelial cells.组织金属蛋白酶抑制剂 2 通过调节基质金属蛋白酶 2 介导的内皮屏障功能障碍和乳腺癌细胞穿过肺微血管内皮细胞的迁移。
Mol Cancer Res. 2010 Jul;8(7):939-51. doi: 10.1158/1541-7786.MCR-09-0523. Epub 2010 Jun 22.
5
RECK negatively regulates matrix metalloproteinase-9 transcription.RECK负向调节基质金属蛋白酶-9的转录。
Cancer Res. 2009 Feb 15;69(4):1502-8. doi: 10.1158/0008-5472.CAN-08-2635. Epub 2009 Feb 10.
6
MT1-MMP and RECK are involved in human CD34+ progenitor cell retention, egress, and mobilization.基质金属蛋白酶-1(MT1-MMP)和RECK参与人类CD34+祖细胞的保留、迁出和动员。
J Clin Invest. 2009 Mar;119(3):492-503. doi: 10.1172/JCI36541. Epub 2009 Feb 9.
7
Correlation between MMPs and their inhibitors in breast cancer tumor tissue specimens and in cell lines with different metastatic potential.乳腺癌肿瘤组织标本以及具有不同转移潜能的细胞系中基质金属蛋白酶与其抑制剂之间的相关性。
BMC Cancer. 2009 Jan 14;9:20. doi: 10.1186/1471-2407-9-20.
8
Breast cancer progression: insights into multifaceted matrix metalloproteinases.乳腺癌进展:对多面性基质金属蛋白酶的见解
Clin Exp Metastasis. 2007;24(8):647-56. doi: 10.1007/s10585-007-9113-7. Epub 2007 Oct 30.
9
HER-2/neu represses the metastasis suppressor RECK via ERK and Sp transcription factors to promote cell invasion.HER-2/neu通过ERK和Sp转录因子抑制转移抑制因子RECK,从而促进细胞侵袭。
J Biol Chem. 2006 Feb 24;281(8):4718-25. doi: 10.1074/jbc.M510937200. Epub 2005 Dec 23.
10
Expression of reversion-inducing-cysteine-rich protein with Kazal motifs (RECK) as a prognostic indicator in gastric cancer.具有Kazal基序的逆转诱导富含半胱氨酸蛋白(RECK)在胃癌中作为预后指标的表达
Eur J Cancer. 2006 Jan;42(1):101-8. doi: 10.1016/j.ejca.2005.09.016. Epub 2005 Dec 1.

RECK 低表达提示浸润性乳腺癌患者的生存时间更短。

Low expression of RECK indicates a shorter survival for patients with invasive breast cancer.

机构信息

Department of Medical Oncology, The Third Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

Cancer Sci. 2012 Jun;103(6):1084-9. doi: 10.1111/j.1349-7006.2012.02265.x. Epub 2012 Apr 19.

DOI:10.1111/j.1349-7006.2012.02265.x
PMID:22404079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7685079/
Abstract

Expression cloning was used to initially isolate the reversion-inducing cysteine-rich protein with Kazal motifs (RECK) gene as a suppressor of transformation. The gene was found to encode a membrane-anchored regulator of MMPs. Experimental studies showed that RECK can suppress tumor invasion, metastasis, and angiogenesis. However, the clinical impact of RECK remains unclear. To assess the clinical significance of RECK expression in invasive breast cancer, a total of 119 patients with invasive breast cancer were retrospectively examined. Expression of RECK in tumor tissues was assessed by immunohistochemical staining. A significant correlation between RECK expression and 5-year survival rate was documented. The 5-year survival rate for patients with strong RECK expression was significantly higher than that for patients with weakly expressing tumors. Univariate and multivariate analyses confirmed that reduced RECK expression was an independent and significant factor in predicting a poor prognosis. In conclusion, RECK expression is a significant prognostic factor correlated with long-term survival for patients with invasive breast cancer. RECK expression is therefore a potentially useful prognostic marker for breast cancer.

摘要

采用表达克隆的方法,最初分离出具有 Kazal 基序的反转诱导富含半胱氨酸的蛋白(RECK)基因作为转化的抑制剂。该基因编码一种 MMPs 的膜锚定调节剂。实验研究表明,RECK 可抑制肿瘤侵袭、转移和血管生成。然而,RECK 的临床意义尚不清楚。为了评估 RECK 在浸润性乳腺癌中的表达的临床意义,对 119 例浸润性乳腺癌患者进行了回顾性检查。通过免疫组织化学染色评估 RECK 在肿瘤组织中的表达。记录到 RECK 表达与 5 年生存率之间存在显著相关性。RECK 表达强的患者的 5 年生存率明显高于肿瘤表达弱的患者。单因素和多因素分析证实,RECK 表达减少是预测预后不良的独立和显著因素。总之,RECK 表达是与浸润性乳腺癌患者长期生存相关的重要预后因素。因此,RECK 表达是乳腺癌潜在的有用预后标志物。