全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
-  2015 

甲状腺乳头状癌中MMP2、COX-2、VEGF和MVD的表达及临床意义
Expressions of MMP2, COX-2, VEGF and MVD in papillary thyroid carcinoma and their clinical significance

DOI: 10.7652/jdyxb201503015

Keywords: 甲状腺乳头状癌,环氧合酶-2,血管内皮生长因子,基质金属蛋白酶,微血管密度
cycloxygenase-2 (COX-2)
,vascular endothelial growth factor (VEGF),matrix metalloproteinase (MMP2),micro-vessel density (MVD),papillary thyroid carcinoma

Full-Text   Cite this paper   Add to My Lib

Abstract:

摘要:目的 研究甲状腺乳头状癌(PTC)中环氧合酶-2(COX-2)、血管内皮生长因子(VEGF)、基质金属蛋白酶(MMPs)表达和微血管密度(MVD)计数与PTC的临床病理特征之间的关系,并用以评估恶性程度、预后。方法 运用免疫组化染色方法,检测32例PTC和18例正常甲状腺组织中的COX-2、VEGF、MMP2表达和MVD计数,并分析其与临床病理特征的关系。结果 COX-2、VEGF、MMP2和MVD在PTC中的表达分别为(中位数和四分位距表示):M(Q3-Q1)=5(1),M(Q3-Q1)=5.5(2),M(Q3-Q1)=5.5(1)和M(Q3-Q1)=28(5.75),与对照组相比差异均有统计学意义(P<0.05)。 COX-2、VEGF、MMP2、MVD的计数表达与患者的年龄、临床分期、淋巴结转移有关(P<0.05);COX-2与VEGF还与性别有关(P<0.05);VEGF、MMP2的表达及MVD的计数还与患者肿瘤大小有关(P<0.05)。COX-2、VEGF、MMP2和MVD在被膜浸润组中的表达分别为:M(Q3-Q1)=6(2),M(Q3-Q1)=6.5(2),M(Q3-Q1)=6(1.75)和M(Q3-Q1)=30(7.75),被膜未浸润组中的表达为:M(Q3-Q1)=5(1.75),M(Q3-Q1)=5(1.75),M(Q3-Q1)=5(1.75)和M(Q3-Q1)=26.5(4);COX-2、VEGF、MMP2和MVD在被膜浸润组与未浸润组之间的表达差异具有统计学意义(P<0.05)。PTC中COX-2、MMP2、VEGF和MVD的表达相互之间具有显著的正相关性(r>0.5)。结论 甲状腺组织中MMP2、COX-2、VEGF的高表达可能促进了PTC的发生和肿瘤淋巴结转移;这与调控肿瘤新生血管有关。检测其表达对评估PTC的恶性程度及预后有一定意义。
ABSTRACT: Objective To investigate the expressions of cycloxygenase-2 (COX-2), vascular endothelial growth factor (VEGF), matrix metalloproteinase (MMP2) and micro-vessel density (MVD) in papillary thyroid carcinoma (PTC) and the relationship between their expressions and clinicopathological features, so as to evaluate the malignancy and prognosis of PTC. Methods The expressions of COX-2, MMP2 and VEGF and MVD count in 32 cases of PTC and 18 cases of normal thyroid tissues were detected by immunohistochemical staining. Their relationship with clinicopathological characteristics was analyzed. Results ① The expression of COX-2, MMP2, VEGF and MVD in PTC was as follows: M(Q3-Q1)=5(1), M(Q3-Q1)=5.5(2), M(Q3-Q1)=5.5(1) and M(Q3-Q1)=28(5.75), respectively. It differed significantly from that in control group (P<0.05). ② The expression of COX-2 in PTC was related to the sex and age of patients, clinical stage and lymph node metastasis (P<0.05). The expression of VEGF in PTC was related to the sex and age of patients, tumor size, clinical stage and lymph node metastasis (P<0.05). The expression of MMP2 and MVD count in PTC were related to the age of patients, tumor size, clinical stage and lymph node metastasis (P<0.05). ③ The expression of COX-2, MMP2, VEGF and MVD in PTC with invasion of thyroid capsules was as follows: M(Q3-Q1=6(2), M(Q3-Q1)=6.5(2), M(Q3-Q1)=6(1.75) and M(Q3-Q1=30(7.75). The expression of these indexes in negative group was: M(Q3-Q1)=5(1.75), M(Q3-Q1)=5(1.75), M(Q3-Q1)=5(1.75) and M(Q3-Q1)=26.5(4). There was a significant difference between the two groups (P<0.05). ④ There was a close positive correlation between the expressions of VEGF, COX-2, MMP2 and MVD in PTC (r>0.5). Conclusion The high expressions of COX-2,

References

[1]  GREENHOUGH A, SMARTT HJ, MOORE AE, et al. The COX-2/PGE2 pathway: key roles in the hallmarks of cancer and adaptation to the tumour microenvironment[J]. Carcinogenesis, 2009, 30(3):377-386.
[2]  王菊勇,郭净,郑展. iNOS/COX-2与恶性肿瘤[J]. 现代肿瘤医学,
[3]  王振,李新华,王新军,等. 乳癌组织中BCSG1、MMP-2 及ETS-1蛋白的表达[J]. 郑州大学学报:医学版, 2012, 47(5):704-707.
[4]  NAKAMURA M, ONODA N, NODA S, et al. E-cadherin expression and cell proliferation in the primary tumor and metastatic lymph nodes of papillary thyroid microcarcinoma[J]. Mol Clin Oncol, 2014, 2(2):226-232.
[5]  李蕊. VEGF对人肝癌细胞体外形成血管生成拟态能力的影响[D]. 天津医科大学, 2012.
[6]  KRYSAN K, DALWADI H, SHARMA S, et al. Cyclooxygenase 2-dependent expression of survivin is critical for apoptosis resistance in non-small cell lung cancer[J]. Cancer Res, 2004, 64(18):6359-6362.
[7]  SASAKI R. Microvessel count and vascular endothelial growth factor in renal cell carcinoma[J]. Nihon Hinyokika Gakkai Zasshi, 1996, 87(8):1032-1040.
[8]  李晓静. 甲状腺癌临床及病理学特点的回顾性分析[D]. 山东大学,2012.
[9]  2012, 20(1):183-186.
[10]  黄晓静,姚和权,吴晓明,等. 环氧合酶-2抑制剂类抗肿瘤药物研究进展[J].药学与临床研究, 2013, 21(3):251-256.
[11]  王喜梅,孙雷,刘逢吉,等. 环氧化酶和基质金属蛋白酶在甲状腺乳头状癌组织中的增强表达及意义[J]. 肿瘤防治杂志, 2004, (6):593-596.
[12]  吴伟群,何小杰,李延辉,等. VEGF在甲状腺肿瘤中的表达及与肿瘤血管生成的关系[J]. 中国医药科学, 2013, 3(12):23-25.
[13]  姬琛华,刘丽娜,吕申,等. 胃癌Survivin、COX-2蛋白的表达及其相关性分析[J]. 大连医科大学学报, 2008, 30(1):10-13.
[14]  王化修,李景和,肖小芹. 甲状腺癌组织MVD和β-连环素蛋白表达及其相关性研究[J]. 现代生物医学进展, 2008, 8(7):1276-1279.
[15]  MAEDA K, CHUNG YS, TAKATSUKA S, et al. Tumor angiogenesis as a predictor of recurrence in gastric carcinoma[J]. J Clin Oncol, 1995, 13(2):477-481.
[16]  华特波,孟宪瑛,张强,等. COX-2、MMP-9、VEGF在甲状腺肿瘤中的表达[J]. 中国老年学杂志, 2011, 31(9):1520-1522.
[17]  卢凤迎,廖新红,李智贤,等. 微血管密度在经直肠超声血流动力学检测鉴别诊断前列腺癌和慢性前列腺炎中的应用及其评价[J]. 吉林大学学报:医学版, 2014, 40(5):1104-1108.
[18]  石磊,赖铭裕,梁志海,等. 胃癌组织中COX-2、VEGF和MVD的表达及其临床意义[J]. 广东医学, 2011, 32(8):1004-1006.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133