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本文引用的文献

1
Vasohibin-1 as a Novel Prognostic Factor for Head and Neck Squamous Cell Carcinoma.血管抑制素-1作为头颈部鳞状细胞癌的一种新型预后因素
Anticancer Res. 2017 Mar;37(3):1219-1225. doi: 10.21873/anticanres.11437.
2
Increased vasohibin-1 expression is associated with metastasis and poor prognosis of renal cell carcinoma patients.血管抑肽-1 表达增加与肾细胞癌患者的转移和不良预后相关。
Lab Invest. 2017 Jul;97(7):854-862. doi: 10.1038/labinvest.2017.26. Epub 2017 Mar 13.
3
Japanese Classification of Esophageal Cancer, 11th Edition: part II and III.《日本食管癌分类》第11版:第二部分和第三部分
Esophagus. 2017;14(1):37-65. doi: 10.1007/s10388-016-0556-2. Epub 2016 Nov 10.
4
Japanese Classification of Esophageal Cancer, 11th Edition: part I.《日本食管癌分类第11版:第一部分》
Esophagus. 2017;14(1):1-36. doi: 10.1007/s10388-016-0551-7. Epub 2016 Nov 10.
5
Vasohibin-2 is required for epithelial-mesenchymal transition of ovarian cancer cells by modulating transforming growth factor-β signaling.血管抑制素-2通过调节转化生长因子-β信号传导,对卵巢癌细胞的上皮-间质转化是必需的。
Cancer Sci. 2017 Mar;108(3):419-426. doi: 10.1111/cas.13157.
6
Targeting human vasohibin-2 by a neutralizing monoclonal antibody for anti-cancer treatment.通过一种中和性单克隆抗体靶向人血管抑制素-2用于抗癌治疗。
Cancer Sci. 2017 Mar;108(3):512-519. doi: 10.1111/cas.13149.
7
Vasohibin 2 promotes human luminal breast cancer angiogenesis in a non-paracrine manner via transcriptional activation of fibroblast growth factor 2.血管抑制素2通过成纤维细胞生长因子2的转录激活以非旁分泌方式促进人腔面型乳腺癌血管生成。
Cancer Lett. 2016 Dec 28;383(2):272-281. doi: 10.1016/j.canlet.2016.09.031. Epub 2016 Oct 1.
8
Proteolytic inactivation of anti-angiogenic vasohibin-1 by cancer cells.癌细胞对抗血管生成因子血管抑制素-1的蛋白水解失活作用。
J Biochem. 2016 Oct;160(4):227-232. doi: 10.1093/jb/mvw030. Epub 2016 May 11.
9
Comprehensive Registry of Esophageal Cancer in Japan, 2009.2009年日本食管癌综合登记处
Esophagus. 2016;13:110-137. doi: 10.1007/s10388-016-0531-y. Epub 2016 Mar 29.
10
Angiogenesis inhibitors in gastric and gastroesophageal junction cancer.胃癌和胃食管交界癌中的血管生成抑制剂
Gastric Cancer. 2016 Jan;19(1):31-41. doi: 10.1007/s10120-015-0537-5. Epub 2015 Sep 2.

血管抑制素-1和-2的表达预示着食管鳞状细胞癌患者的预后不良。

Expression of vasohibin-1 and -2 predicts poor prognosis among patients with squamous cell carcinoma of the esophagus.

作者信息

Ninomiya Yamato, Ozawa Soji, Oguma Junya, Kazuno Akihito, Nitta Miho, Kajiwara Hiroshi, Sato Yasufumi

机构信息

Department of Gastroenterological Surgery, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.

Department of Pathology, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.

出版信息

Oncol Lett. 2018 Oct;16(4):5265-5274. doi: 10.3892/ol.2018.9249. Epub 2018 Aug 1.

DOI:10.3892/ol.2018.9249
PMID:30250596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6144939/
Abstract

Vasohibin (VASH) -1 and -2 are novel angiogenic regulators. The aim of the present study was to assess the prognostic values of VASH1 expression and VASH2 expression in esophageal squamous cell carcinoma (ESCC). A total of 209 patients with ESCC were investigated. Resected tumor specimens were immunostained using anti-CD34 antibody, anti-VASH1 antibody and anti-VASH2 antibody. The ratio of the microvessels density and the VASH1 density as the VASH1-positive ratio were defined and the patients were divided into two groups (a high VASH1 group and a low VASH1 group) according to the average value. The patients were also divided into two groups (a high VASH2 group and a low VASH2 group) according to VASH2 expression upon immunostaining. The clinical outcomes of these two groups were then evaluated. The high VASH1 group contained 106 patients (50.7%). The high VASH2 group contained 48 patients (23.0%). Long-term survival was significantly poorer in the high VASH1 group compared with that in the low VASH1 group. A slight correlation between VASH1 expression and VASH2 expression was observed. The low VASH1/low VASH2 group had a better prognosis than the other three groups with different combinations of VASH1 and VASH2 expression levels. The present study showed that high VASH1 expression and high VASH2 expression may be novel independent predictors of a poor prognosis in patients with ESCC and that a slight correlation between VASH1 and VASH2 expression existed. The present findings suggest that combined evaluation of VASH1 and VASH2 expression should provide an improved understanding of their clinicopathological features.

摘要

血管抑制素(VASH)-1和-2是新型血管生成调节因子。本研究旨在评估VASH1表达和VASH2表达在食管鳞状细胞癌(ESCC)中的预后价值。共对209例ESCC患者进行了研究。使用抗CD34抗体、抗VASH1抗体和抗VASH2抗体对切除的肿瘤标本进行免疫染色。定义微血管密度与VASH1密度之比即VASH1阳性率,并根据平均值将患者分为两组(高VASH1组和低VASH1组)。还根据免疫染色时的VASH2表达将患者分为两组(高VASH2组和低VASH2组)。然后评估这两组的临床结局。高VASH1组有106例患者(50.7%)。高VASH2组有48例患者(23.0%)。高VASH1组的长期生存率明显低于低VASH1组。观察到VASH1表达与VASH2表达之间存在轻微相关性。低VASH1/低VASH2组的预后优于其他三组VASH1和VASH2表达水平不同组合的患者。本研究表明,高VASH1表达和高VASH2表达可能是ESCC患者预后不良的新型独立预测指标,且VASH1与VASH2表达之间存在轻微相关性。本研究结果表明,联合评估VASH1和VASH2表达应能更好地了解其临床病理特征。