期刊文献+

STAT3、VEGF在良恶性嗜铬细胞瘤中的表达及其与血管生成的关系 被引量:4

Correlation of STAT3 and VEGF expressions with angiogenesis in pheochromocytoma
暂未订购
导出
摘要 目的通过检测信号转导和转录激活因子-3(STAT3)、血管内皮生长因子(VEGF)、微血管密度(MVD)在良、恶性嗜铬细胞瘤中的表达情况,探讨STAT3、VEGF能否成为一种预判恶性嗜铬细胞瘤的指标和肿瘤治疗的潜在靶点。方法选取1986年10月至2006年8月住院经手术治疗、且有完整的临床、病理和随访资料的嗜铬细胞瘤患者存档石蜡标本38例,其中良性嗜铬细胞瘤(良性组)21例,恶性嗜铬细胞瘤(恶性组)17例。恶性组首次手术确诊为嗜铬细胞瘤后随访4~155个月,良性组首次手术确诊为嗜铬细胞瘤后随访69~240个月;采用免疫组织化学技术,检测良性组、恶性组中STAT3、VEGF和MVD的表达情况。结果 STAT3在恶性组中的阳性表达率为70.6%,明显高于良性组中的阳性表达率(23.8%),两组间STAT3的表达具有显著的统计学差异(P<0.05)。VEGF在恶性组中的阳性表达率为82.4%,明显高于良性组中的阳性表达率(23.8%),且表达具有统计学意义(P<0.05)。MVD在恶性组中的阳性表达为36.41±13.00,良性组中为21.43±8.05,两者之间有显著性统计学意义(P<0.05)。在嗜铬细胞瘤中,STAT3与VEGF的表达以及VEGF与MVD的表达均呈正相关。结论 STAT3和VEGF有望成为预判嗜铬细胞瘤良、恶性的一种指标,并且有望成为肿瘤治疗的潜在靶点。 Objective To explore the expressions of STAT3,VEGF,microvessel density (MVD) and their relationships in benign and malignant pheochromoeytoma,so as to discuss the potential role of STAT3 and VEGF as useful markers of malignant pheoehromoeytoma. Methods Data of 38 patients with pheoehromoeytoma from Oct. 1986 to Aug. 2006 were studied retrospectively. 21 cases were diagnosed as benign neoplasms and the others were malignant. The expressions of STAT3,VEGF and MVD were analyzed in all these cases with immunohistochemical method. The benign cases were followed up for 69 to 240 months,while the malignant cases 4 to 155 months. Results Both STAT3 and VEGF highly expressed in the malignant cases, but lowly expressed in the benign ones,with significant difference (P〈0. 05). Moreover, the expression of MVD was higher in the malignant cases than in the benign cases, with significant difference (P〈0.05). The expressions of STAT3 and VEGF were positively correlated with MVD. Conclusions STAT3 and VEGF in pheoehromocytoma contribute to tumor angiogenesis. The expressions of STAT3 and VEGF may play an important role as useful markers in the diagnosis of malignant pheochromoeytoma.
出处 《现代泌尿外科杂志》 CAS 2012年第5期439-442,共4页 Journal of Modern Urology
基金 上海市自然科学基金(No.09ZR1418500) 上海市教委科研创新项目(No.11YZ58)
关键词 嗜铬细胞瘤 信号转导和转录激活因子-3(STAT3) 血管内皮生长因子(VEGF) 微血管密度(MVD) 免疫组化 pheochromocytoma STAT3 VEGF microvessel density immunohistochemistry
  • 相关文献

参考文献2

二级参考文献117

  • 1王金万,孙燕,刘永煜,于起涛,张沂平,李凯,朱允中,周清华,侯梅,管忠震,李维廉,庄武,王东林,梁后杰,秦凤展,卢辉山,刘晓晴,孙红,张燕军,王杰军,罗素霞,杨瑞合,涂远荣,王秀问,宋恕平,周静敏,游丽芬,王竞,姚晨.重组人血管内皮抑素联合NP方案治疗晚期NSCLC随机、双盲、对照、多中心Ⅲ期临床研究[J].中国肺癌杂志,2005,8(4):283-290. 被引量:630
  • 2Ruff-Jamison S, Zhong Z, Wen Z, et al. Epidermal growth factor and lipopolysaccharide activate Stat3 transcription factor in mouse liver. J Biol Chem 1994; 269:21933-5.
  • 3Yu CL, Meyer D J, Campbell GS, et al. Enhanced DNA-binding activity of a Stat3-related protein in cells transformed by the Src oncoprotein. Science 1995; 269:81-3.
  • 4Su Wc, Kitagawa M, Xue N, et al. Activation of Stat 1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia typeⅡ dwarfism. Nature 1997; 386:288-92.
  • 5Chin YE, Kitagawa M, Su WC, et al. Cell growth arrest and induction of cyclin-dependent kinase inhibitor p21 WAF 1/C1P 1 mediated by STAT1. Science 1996; 272:719-22.
  • 6Chin YE, Kitagawa M, Kuida K, Flavell RA, Fu XY. Activation of the STAT signaling pathway can cause expression of caspase 1 and apoptosis. Mol Cell Biol 1997; 17:5328-37.
  • 7Kortylewski M, Kujawski M, Wang T, et al. Inhibiting Stat3 signaling in the hematopoietic system elicits multicomponent antitumor immunity. Nat Med 2005; 11:1314-21.
  • 8Blumberg RS, Strober W. Prospects for research in inflammatory bowel disease. JAMA 2001; 285:643-7.
  • 9Plevy SE, Landers C J, Prehn J, et al. A role for TNF-alpha and mueosal T helper-1 cytokines in the pathogenesis of Crohn's disease. J Immunol 1997; 159:6276-82.
  • 10Kosiewicz M M, Nast CC, Krishnan A, et al. Th 1-type responses mediate spontaneous ileitis in a novel murine model of Crohn's disease. J Clin Invest 2001; 107:695-702.

共引文献21

同被引文献69

  • 1童安莉,曾正陪,杨堤,李汉忠,李明,陈松,孙梅励.人嗜铬细胞瘤组织中转化生长因子α、肿瘤坏死因子α和血管内皮生长因子的表达[J].中国医学科学院学报,2004,26(4):426-431. 被引量:6
  • 2赵一鸣,王鲁.血管内皮生长因子受体与肝细胞癌血管生成关系的研究进展[J].世界华人消化杂志,2007,15(6):596-600. 被引量:9
  • 3Clark JC, Thomas DM, Chong PF,et al. RECK-anewly discovered inhibitor of metastasis with prog-nostic significance in multiple forms of cancer [J].Cancer Metastasis Rev,2007 ,26(5) :675 —683.
  • 4Stepkowski SM,Chen W,Ross JA,et al. STAT3 : animportant regulator of multiple cytokine functions[J]. Transplantation.2008,85(10): 1372 — 1377.
  • 5Neppelberg E,Johannessen AC,Jonsson R. Apopto-sis in oral lichen planus[J], Eur J Oral Sci,2001,109(5):361-364.
  • 6Weerasinghe P, Garcia GE, Zhu Q, et al. Inhibitionof stat3 activation and tumor growth suppresion ofnon-small cell lung cancer by G-quartet oligonucle-otides [J]. Int J Oncol,2007,31(1):129 —134.
  • 7ZUBER S M, KANTOROVICH V, PACAK K. Hypertension in pheochromocytoma: characteristics and treatment [ J ]. Endocrinol Metab Clin North Am,2011,40 (2) :295-311.
  • 8AMAR L, BERTHERAT J, BAUDIN E, et al. Genetic testing in pheochromocytoma or functional paraganglioma [ J ]. J CHn Oncol, 2005,23 ( 34 ) : 8812-8818.
  • 9LIPS C J, HOPPENER J W, VAN NEASELROOIJ B P, et al. Counselling in multiple endocrine neoplosia syndromes: from individual experience to general guidelines [J]. J Intern Med,2005,257( 1 ) :69-77.
  • 10MARTUCCIELLO G, LERONE M,BRICCO L, et al. Multiple endocrine neoplasias type 2B and RET proto- oncogene [J]. Ital J Pediatr,2012,38:9.

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部