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血清MMP-2在甲状腺乳头状癌复发或残留者中的表达研究

Expression of Serum MMP-2 in Patients with Papillary Thyroid Cancer Recurrence or Residuum
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摘要 目的探讨基质金属蛋白酶(MMP)-2在甲状腺乳头状癌(PTC)复发或残留患者血清中的表达水平及其临床应用价值。方法采集2009年3月至2009年12月期间入住我科行手术治疗的68例甲状腺疾病患者的术前空腹血清和15位体检健康者的空腹血清。根据术后病理结果分为PTC伴淋巴结转移组(19例)、PTC复发或残留伴淋巴结转移组(17例)、PTC无淋巴结转移组(10例)、甲状腺良性疾病组(22例),体检健康者作为对照组(15位),采用ELISA法测定各组血清标本中MMP-2的表达水平,并分析各组MMP-2表达水平的差异。结果血清MMP-2表达水平在PTC复发或残留伴淋巴结转移组、PTC伴淋巴结转移组、PTC无淋巴结转移组、甲状腺良性疾病组及对照组中分别为(1 724.00±762.24)ng/ml、(1 329.16±776.59)ng/ml、(1 489.61±546.53)ng/ml、(1 264.87±817.27)ng/ml及(608.43±88.63)ng/ml,PTC复发或残留伴淋巴结转移组和PTC伴淋巴结转移组均分别明显高于甲状腺良性疾病组和对照组(P<0.05);PTC无淋巴结转移组仅明显高于对照组(P<0.05),而与甲状腺良性疾病组比较,差异无统计学意义(P>0.05)。甲状腺良性疾病组与对照组间比较差异也无统计学意义(P>0.05);3个恶性疾病组间MMP-2表达水平比较差异无统计学意义(P>0.05)。PTC伴淋巴结转移组、PTC复发或残留伴淋巴结转移组、PTC无淋巴结转移组、甲状腺良性疾病组及对照组的MMP-2表达阳性率分别为79%、76%、80%、41%及20%。3个恶性疾病组间阳性率比较差异均无统计学意义(P>0.05),但均分别明显高于甲状腺良性疾病组和对照组(P<0.01)。甲状腺良性疾病组的阳性率也明显高于对照组(P<0.01)。结论血清MMP-2的检测可以用于术前甲状腺包块性质判断的筛选指标;血清MMP-2水平检测不适用于判断PTC是否转移。 Objective To explore the expression of matrix metalloproteinase (MMP) -2 in patients with papillary thyroid cancer (PTC) recurrence or residuum and its value of clinical application. Methods The serums from 68 patients with thyroid disease underwent operation and 15 health examinations under stomachs empty from March 2009 to December 2009 in this hospital were gathered. Sixty-eight patients with thyroid disease were divided into PTC with lymph node metastasis (LNM) group (n=19), PTC recurrence or residuum with LNM group (n=17), PTC without LNM group (n 10), and benign thyroid disease group (n=22) according to the postoperative pathological findings, 15 health examinations as control group. The expression of MMP-2 of serum sample was detected by ELISA method. The difference of the expression of MMP-2 in each group was analyzed. Results The expressions of MMP-2 in the PTC recurrence or residuum with LNM group, PTC with LNM group, PTC without LNM group, benign thyroid disease group, and the control group were (1 724. 00±762.24) ng/ml, (1 329. 16±776.59) ng/ml, (1 489.61±546. 53) ng/ml, (1 264.87±817.27) ng/ml, and (608.43 ± 88.63) ng/ml, respectively. The expressions of MMP-2 in the PTC with LNM group and PTC recurrence or residuum with LNM group were significantly higher than those in the benign thyroid disease group (P〈 0.05) and the control group (P 〈 0.05), respectively, which in the PTC without LNM group was significantly higher than that in the control group (P〈 0.05). There was no significant difference of MMP-2 expression of serum between the benign thyroid disease group and the control group (P〉0. 05), which were no significant difference among the other three malignant disease groups (P〉0. 05). The MMP-2 positive expression rates were 79%, 76%, 80%, 41%, and 20% in the PTC with LNM, PTC recurrence or residue with LNM group, PTC without LNM group, benign thyroid disease group, and control group, respectively. The MMP-2 positive expressions rates of serums were not significantly different among three malignant disease groups (P〉0. 05), but which were significantly higher than those of the benign thyroid disease group (P〈 0. 01) and control group (P〈 0. 01), respectively. Conclusions The MMP-2 level of serum can be used as an index to judge preoperative thyroid nodules, which can not be use to determine whether PTC metastasis or not.
作者 黄勇 程若川
出处 《中国普外基础与临床杂志》 CAS 2012年第8期864-867,共4页 Chinese Journal of Bases and Clinics In General Surgery
关键词 甲状腺乳头状癌 淋巴结转移 复发 转移 基质金属蛋白酶-2 Papillary thyroid cancer Lymph node metastasis Recurrence Residuum Matrix metallopro- teinase-2
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参考文献25

  • 1江现强,刘志明,赫军,陆云飞.MMP-2在甲状腺癌中的表达及其临床意义[J].广西医科大学学报,2005,22(6):868-870. 被引量:3
  • 2万正东,陆云飞,刘志明.MMP-2、MMP-7在甲状腺乳头状癌中的表达及其临床意义[J].广西医科大学学报,2008,25(5):677-679. 被引量:2
  • 3Nakamura H, Ueno H, Yamashita K, et al. Enhanced production and activation of progelatinase A mediated by membrane-type 1 matrix metalloproteinase in human papillary thyroid carcinomas [J]. Cancer Res, 1999, 59(2): 467-473.
  • 4Purcell WT, Michelle AR, Manuel H. Development of matrix metalloproteinase inhibitors in cancer therapy [J]. J Natl Cancer Inst, 2002, 16(5): 1189-1227.
  • 5周少飞,李扬,丁红光.血清中MMP-2和MMP-9与乳头状甲状腺癌的关系[J].河北医药,2008,30(1):6-7. 被引量:3
  • 6Liotta LA, Stetler-Stevenson WG. Tumor invasion and metastasis: an imbalance of positive and negative regulation [J]. Cancer Res, 1991, 51(18 Suppl): 5054s-5059s.
  • 7Westermarck J, Kahari VM. Regulation of matrix metalloproteinase expression in tumor invasion [J]. FASEB J, 1999, 13(8): 781-792.
  • 8Shiomi T, Okada Y. MT1-MMP and MMP-7 in invasion and metastasis of human cancers [J]. Cancer Metastasis Rev, 2003, 22(2-3): 145-152.
  • 9Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinasesl structure, function, and biochemistry [J]. Circ Res, 2003, 92(8): 827-839.
  • 10Tayebjee MH, Lim HS, Macfadyen RJ, et al. Matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 and-2 in type 2 diabetes: effect of 1 year's cardiovascular risk reduction therapy [J]. Diabetes Care, 2004, 27(8): 2049-2051.

二级参考文献25

  • 1Shiomi T, Okada Y. MT1-MMP and MMP-7 in invasion and metastasis of human cancers[J]. Cancer Metastasis Rev, 2003,22(2-3): 145-152.
  • 2Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry[J]. Circ Res, 2003,92(8): 827-839.
  • 3Misugi F, Sumi T. Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinase in uterine endometrial carcinoma and a correlation between ex pression of matrix metalloproteinase-7 and prognosis [J]. Int J Mol Med, 2005,16(4) :541-546.
  • 4Koyama S. Enhanced cell surface expression of matrix metalloproteinases and their inhibitors, and tumor-induced host response in progression of human gastric carcinoma[J]. Dig Dis Sci, 2004, 49(10):1 621-1 630.
  • 5Wang FQ, So J. Matrilysin (MMP-7) promotes invasion of ovarian cancer cells by activation of progelatinase[J]. Int J Cancer, 2005,114(1):19-31.
  • 6Siironen P, Louhimo J. Prognostic factors in papillary thyroid cancer: an evaluation of 601 consecutive patients[J]. Tumour Biol, 2005,26 (2): 57-64.
  • 7Korem S, Kraiem Z. Increased expression of matrix metalloproteinase-2: a diagnostic marker but not prognostic marker of papillary thyroid carcinoma [J]. Isr Med Assoc J, 2002,4(4) :247-251.
  • 8Powell WC, Fingleton B, Wilson CL,et al. The metalloproteinase matrilysin proteolytically generates active soluble Fas ligand and potentiates epithelial cell apoptosis[J]. Curr Biol ,1999,9:1 441-1 447.
  • 9Hidalgo M, Eckhardt SG. Development of matrix metalloproteinase inhibitors in cancer therapy[J]. J Natl Cancer Inst, 2001,93 (3) :178-193.
  • 10Kinder,Barbara KMD.Well differentiated thyroid cancer.Current Opinion in Oncology,2003,15(1):71-77.

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