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本文引用的文献

1
Elevated expression of KLK8 predicts poor prognosis in colorectal cancer.KLK8的高表达预示着结直肠癌的预后不良。
Biomed Pharmacother. 2017 Apr;88:595-602. doi: 10.1016/j.biopha.2017.01.112. Epub 2017 Jan 28.
2
Decrease of serum Angiotensin converting enzyme levels upon telbivudine treatment for chronic hepatitis B virus infection and negative correlations between the enzyme levels and estimated glumerular filtration rates.替比夫定治疗慢性乙型肝炎病毒感染后血清血管紧张素转换酶水平降低以及该酶水平与估计肾小球滤过率之间的负相关性。
Hepat Mon. 2014 Jan 31;14(1):e15074. doi: 10.5812/hepatmon.15074. eCollection 2014 Jan.
3
Randomized clinical trial: efficacy and safety of telbivudine and lamivudine in treatment-naïve patients with HBV-related decompensated cirrhosis.随机临床试验:替比夫定和拉米夫定治疗初治 HBV 相关失代偿期肝硬化患者的疗效和安全性。
J Viral Hepat. 2012 Oct;19(10):732-43. doi: 10.1111/j.1365-2893.2012.01600.x. Epub 2012 Mar 15.
4
Human kallikrein 8 expression in salivary gland tumors.人组织激肽释放酶8在涎腺肿瘤中的表达
Head Neck Pathol. 2008 Sep;2(3):169-74. doi: 10.1007/s12105-008-0068-z. Epub 2008 Jul 3.
5
Alternative splicing variant of kallikrein-related peptidase 8 as an independent predictor of unfavorable prognosis in lung cancer.激肽释放酶相关肽酶 8 的剪接变体作为肺癌不良预后的独立预测因子。
Clin Chem. 2010 Jun;56(6):987-97. doi: 10.1373/clinchem.2009.138917. Epub 2010 Apr 1.
6
Expression and prognostic significance of kallikrein-related peptidase 8 protein levels in advanced ovarian cancer by using automated quantitative analysis.运用自动定量分析检测激肽释放酶相关肽酶8蛋白水平在晚期卵巢癌中的表达及其预后意义
Thromb Haemost. 2009 Mar;101(3):541-6.
7
Multiple kallikrein (KLK 5, 7, 8, and 10) expression in squamous cell carcinoma of the oral cavity.多种激肽释放酶(KLK 5、7、8和10)在口腔鳞状细胞癌中的表达
Histol Histopathol. 2009 Feb;24(2):197-207. doi: 10.14670/HH-24.197.
8
2-Year GLOBE trial results: telbivudine Is superior to lamivudine in patients with chronic hepatitis B.GLOBE试验两年结果:在慢性乙型肝炎患者中,替比夫定优于拉米夫定。
Gastroenterology. 2009 Feb;136(2):486-95. doi: 10.1053/j.gastro.2008.10.026. Epub 2008 Nov 1.
9
Human kallikrein 8 protease confers a favorable clinical outcome in non-small cell lung cancer by suppressing tumor cell invasiveness.人激肽释放酶8蛋白酶通过抑制肿瘤细胞侵袭性,赋予非小细胞肺癌良好的临床预后。
Cancer Res. 2006 Dec 15;66(24):11763-70. doi: 10.1158/0008-5472.CAN-06-3165.
10
Expression of tumor-associated differentially expressed Gene-14 (TADG-14/KLK8) and its protein hK8 in uterine endometria and endometrial carcinomas.
Tumour Biol. 2006;27(5):274-82. doi: 10.1159/000094741. Epub 2006 Jul 28.

长期替比夫定治疗后血清激肽释放酶-8水平升高。

Increase of Serum Kallikrein-8 Level After Long-term Telbivudine Treatment.

作者信息

Wang Haw-En, Lin Chih-Lang, Pan Tai-Long, Yeh Chau-Ting

机构信息

Liver Research Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan, R.O.C.

Liver Research Unit, Keelung Chang Gung Memorial Hospital, Keelung, Taiwan, R.O.C.

出版信息

In Vivo. 2018 Jul-Aug;32(4):955-960. doi: 10.21873/invivo.11334.

DOI:10.21873/invivo.11334
PMID:29936485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6117777/
Abstract

BACKGROUND/AIM: Our previous cDNA microarray study revealed increased cellular mRNA levels of a panel of genes, including kallikrein-8 (KLK8), after long-term telbivudine treatment in chronic hepatitis B patients. The aim of this study was to verify whether serum protein levels of KLK8, a cancer-related enzyme, are indeed increased after telbivudine treatment.

PATIENTS AND METHODS

A total of 83 chronic hepatitis B patients receiving telbivudine for >2 years were retrospectively analyzed. Serum KLK8 protein and estimated glomerular filtration rate (eGFR) changes were compared before and after treatment.

RESULTS

Both serum KLK8 protein and eGFR increased significantly after long-term telbivudine treatment (paired t-test: KLK8, p<0.001; eGFR, p=0.001). No direct correlation was found between KLK8 increase and eGFR change. However, eGFR change was positively associated with post-treatment KLK8 levels following adjustment for body height (p<0.001).

CONCLUSION

Telbivudine treatment resulted in increased levels of serum KLK8 protein. Furthermore, eGFR increase was associated with body height-adjusted, post-treatment KLK8 levels.

摘要

背景/目的:我们之前的cDNA微阵列研究显示,在慢性乙型肝炎患者长期接受替比夫定治疗后,一组基因(包括激肽释放酶8,KLK8)的细胞mRNA水平升高。本研究旨在验证癌症相关酶KLK8的血清蛋白水平在替比夫定治疗后是否确实升高。

患者与方法

对83例接受替比夫定治疗超过2年的慢性乙型肝炎患者进行回顾性分析。比较治疗前后血清KLK8蛋白和估计肾小球滤过率(eGFR)的变化。

结果

长期替比夫定治疗后,血清KLK8蛋白和eGFR均显著升高(配对t检验:KLK8,p<0.001;eGFR,p=0.001)。未发现KLK8升高与eGFR变化之间存在直接相关性。然而,在调整身高后,eGFR变化与治疗后KLK8水平呈正相关(p<0.001)。

结论

替比夫定治疗导致血清KLK8蛋白水平升高。此外,eGFR升高与调整身高后的治疗后KLK8水平相关。