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Heparanase-1在恶性嗜铬细胞瘤中的表达及其意义 被引量:3

Expression of Heparanase-1 in malignant pheochromocytomas
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摘要 目的:探讨类肝素酶(Heparanase)成为一种预判肾上腺恶性嗜铬细胞瘤指标的可能性。方法:选取经手术治疗且具有完整的临床、病理和随访资料的肾上腺嗜铬细胞瘤患者的存档石蜡标本27例,其中良性嗜铬细胞瘤10例(良性组),恶性嗜铬细胞瘤17例(恶性组)。另取5例因良性肾疾患行肾切除时获取的同侧正常肾上腺组织作为对照组。采用免疫组织化学技术检测良、恶性嗜铬细胞瘤及正常肾上腺髓质组织中Heparanase-1的表达情况。结果:Heparanase-1在肾上腺恶性嗜铬细胞瘤中表达最高(76.5%),在肾上腺良性嗜铬细胞瘤中表达较低(30.0%),在正常肾上腺髓质组织中无表达,恶性组与良性组及恶性组与正常组之间Heparanase-1的表达差异有统计学意义(P<0.05)。结论:Heparanase-1有望成为预判肾上腺恶性嗜铬细胞瘤的一种指标。 Objective:To analyse the value of Heparanase-1 (HPA) as marker for malignant pheochromocyto-mas. Methods: 27 paraffin-embedded specimens included 10 benign pheochromocytomas and 17 malignant pheo-chromocytomas obtained from operations performed in Rui Jin Hospital affiliated to Shanghai Jiao Tong University School of Medicine from 1986 to 2006 with complete clinical, pathological and follow-up records were selected. Ipsilateral normal adrenal glands from 5 cases underwent nephrectomy for benign renal tumors served as a control group. Immunohistochemical technology was performed to detect the HPA in all specimens. Results:In malignant pheochromocytomas, (76.5%) the expression of HPA was strong, in benign pheochromocytomas the expression was relatively weak (30.0%), but in the normal adrenal medulla tissue was negative expression. The expression of HPA between the groups of benign pheochromocytoma and malignant pheochromocytoma, malignant pheochro-mocytoma and normall adrenal medulla tissue showed significant differences (P〈0.05). Conclusions: HPA would become a new predictor marker for malignant pheochromoeytoma.
出处 《临床泌尿外科杂志》 2008年第6期435-437,共3页 Journal of Clinical Urology
关键词 嗜铬细胞瘤 肾上腺肿瘤 肿瘤标志物 免疫组织化学 Pheoehromoeytoma Adrenal tumor Tumor marker Immunohistoehemistry
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参考文献9

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同被引文献32

  • 1张海燕,高大新,温滨红,刘国良.存活素与血管内皮生长因子在甲状腺癌中的表达及其意义[J].中华内分泌代谢杂志,2005,21(3):244-247. 被引量:11
  • 2王顺祥,田志宏,吴晓慧,周少英,彭利.乙酰肝素酶和血管内皮生长因子在肝癌中的表达及其与血管生成的关系[J].中华实验外科杂志,2006,23(1):107-107. 被引量:13
  • 3ELKIN M. Heparanase as mediator of angiogenesis: mode of action [J]. FASEB J, 2001, 15(5) :1661-1663.
  • 4MARCHETTI D, LI J, SHEN R. Astrocytes contribute to the brain metastatic specificity of melanoma cells by producing heparanase [J]. Cancer Res, 2000, 60(9):4767-4770.
  • 5VLODAVSKY I, FRIEDMANN Y, ELKIN M, et al. Mammalian heparanase : gene cloning, expression and function in tumor progression and metastasis [J]. Nat Med, 1999, 5(7):793-802.
  • 6WHITELOCK JM, MURDOCH AD, IOZZO RV, et al. The degradation of human endothelial cell derived perlecan and release of bound basic fibroblast growth factor by stromelysin,collagenase, plasmin, and heparanase [J]. J Biol Chem, 1996, 271(17) :10079-10086.
  • 7HULETT MD, FREEMAN C, HAMDORF BJ, et al. Cloning of mammalian heparanase, an important enzyme in tumor invasion and metastasis [J]. Nat Med, 1999, 5(7) :803-809.
  • 8QUIROS RM, KIN AW, MAXHIMER J, et al. Differential heparanase-1 expression in malignant and benign pheochromocytomas [J]. J Surg Res, 2002, 108(1):44-50.
  • 9MIAO HQ, ELKIN M, AINGORN E, et al. Inhibition of heparanase activity and tumor metastasis by laminarin sulfate and synthetic phosphorothioate oligodeoxynueleotides [J]. Int J Cancer, 1999, 83(3):424-431.
  • 10PARISH CR, FREEMAN C, BROWN KJ, et al. Identification of sulfated oligosaccharide based inhibitors of tumor growth and metastasis using novel in vitro assays for angiogenesis and heparanase activity [J]. Cancer Res, 1999, 59(14):3433-3441.

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