期刊文献+

新辅助化疗对乳腺癌组织因子、基质金属蛋白酶-9和蛋白酶激活受体-2的表达及疗效的影响 被引量:3

The impact of neoadjuvant chemotherapy on the expression of tissue factor,protease activated receptor-2 and matrix metalloproteinase-9
下载PDF
导出
摘要 背景与目的:组织因子(tissue factor,TF)、基质金属蛋白酶-9(matrixmetalloproteinase-9,MMP-9)是影响乳腺癌转移和预后的重要因子,蛋白酶激活受体-2(proteinaseactivated receptor-2,PAR-2)是二者之间的介导因子。本研究旨在探讨乳腺癌组织中TF、PAR-2和MMP-9表达的变化与乳腺癌新辅助化疗疗效的关系。方法:应用二步法免疫组织化学方法检测85例乳腺癌新辅助化疗前后乳腺癌组织中TF、PAR-2和MMP-9的表达,分析新辅助化疗前后其表达的变化与新辅助化疗疗效的关系。结果:85例乳腺癌新辅助化疗患者病理完全缓解率(G5)为8.3%,其他患者在新辅助化疗后TF、PAR-2和MMP-9阳性率均降低,其中MMP-9显著降低(P<0.05)。新辅助化疗后,MMP-9表达阳性减弱的患者病理疗效显著好于阳性增强者(P<0.05);TF、MMP-9由阳性转为阴性患者的病理疗效显著好于由阴性转为阳性患者(P<0.05)。PAR-2的改变则与病理疗效无显著关系。结论:乳腺癌新辅助化疗后TF、MMP-9的阳性表达降低与病理缓解率相关,有助于判断新辅助化疗疗效。 Background and purpose: TF and MMP-9 are important factors for prognosis and metastasis of breast cancer, PAR-2 is the mediate factor of them, this study aimed to evaluate the change of expressions of TF PAR-2 and MMP-9 in breast cancer patients after neoadjuvant chemotherapy and their correlations with pathologic response. Methods: The expressions of TF, PAR-2 and MMP-9 in 85 breast cancer tissues were examined by immunohistochemical technique (SP) before and after neoadjuvant chemotherapy. Correlation analysis were made between the change of expressions and pathologic response. Results: The strictly pathologic completely response rate (G5) was 8.3% in 85 breast cancer patients after neoadjuvant chemotherapy. The decrease of expression of MMP- 9 after neoadjuvant chemotherapy was statistically significant correlations with pathological response (P〈0.05). The expression changes of TF and MMP-9 from positive to negative was statistically significant correlated with tumor pathological response(P〈0.05). The expression change of PAR-2 showed rarely significant (P〉0.05). Conclusion: The decrease of expression of TF and MMP-9 after neoadjuvant chemotherapy have statistically significant correlations with pathological response, would be probably useful for estimating the effect of neoadjuvant chemotherapy.
出处 《中国癌症杂志》 CAS CSCD 北大核心 2013年第3期195-199,共5页 China Oncology
关键词 乳腺癌 组织因子 蛋白酶激活受体-2 基质金属蛋白酶-9 新辅助化疗 Breast cancer TF PAR-2 MMP-9 Neoadjuvant chemotherapy
  • 相关文献

参考文献9

  • 1CONTRINO J, HAIR G, KREUTZER D L, et al. In situ detection of tissue factor in vascular endothelial cells:correlation with the malignant phenotype of human breast disease [ J ] . Nat Med, 1996, 2: 209-215.
  • 2BARTSCH J E, STAREN E D, APPERT H E. Matrix metalloproteinase expression in breast cancer [ J ] . J Surg Res, 2003, 110 (2): 383-392.
  • 3OGSTON KN, MILLER I D, PAYNE S, et al. A new histological grading system to assess response of breast cancers to primary chemotherapy: prognostic significance and survival [ J ] . Breast, 2003, 12: 320-327.
  • 4DUCH J, FUSTER D, MUNOZ M, et al. 18F-FDG PET/CT for early prediction of response to neoadjuvant chemotherapy in breast cancer [ J ] . Eur J Nucl Med Mol Imaging, 2009, 36(10):1551-1557.
  • 5赵建新,林增茂,姚宏伟,万远廉.组织因子和基质金属蛋白酶-9在乳腺癌中的表达与预后分析[J].中国肿瘤临床,2008,35(1):22-25. 被引量:6
  • 6UENO T, TOI M, KOIKE M , et al. Tissue factor expression in breast cancer tissues : its correlation with prognosis and plasma concentration [ J ] . Br J Cancer, 2000, $3(2): 164.
  • 7GIANNELLI G, ERRIQUEZ R, FRANSVEA E, et al. Proteolytic imbalance is reversed after therapeutic surgery in breast cancer patients [ J ] . Int J Cancer, 2005, 116(6): 1000-1001.
  • 8王新友,王岭,陈江浩,姚青,易军,王辉.CEF方案新辅助化疗对乳腺癌患者血浆基质金属蛋白酶-2,-9活性的影响[J].中国现代医学杂志,2006,16(18):2741-2743. 被引量:3
  • 9汤坚强,万远廉,刘玉村,戎龙,汪欣,吴涛,潘义生,叶京明,姚宏伟,朱静.组织因子促进人类大肠癌细胞的侵袭及与基质金属蛋白酶类的相关性研究[J].北京大学学报(医学版),2005,37(3):265-268. 被引量:13

二级参考文献31

  • 1万远廉,戎龙,刘玉村,汪欣,吴涛,潘义生,姚宏伟,叶京明,汤坚强,朱静.组织因子对大肠癌侵袭能力的影响及其与基质金属蛋白酶-9的关系[J].中华实验外科杂志,2004,21(9):1087-1088. 被引量:17
  • 2刘阁玲,张慧芹,李伟娟,齐凤英.MMP-9及TIMP-1mRNA在甲状腺肿瘤中的表达及临床意义[J].中国肿瘤临床,2005,32(11):644-647. 被引量:3
  • 3Ruf W, Edgar GF, Hui H, et al. Diverse functions of protease receptor tissue factor in inflammation and metastasis[ J]. Immunologic Res,2000,21:289 -292
  • 4Versteeg HH, Peppelenbosch MP, Spek CA,et al. Tissue factor signal transduction in angiogenesis [ J ]. Carcinogenesis, 2003,24:1009 - 1013
  • 5Zhang Y, Deng Y, Luther T, et al. Tissue factor controls the balance of angiogenic and antiangiogenic properties of tumor cells in mice [ J ]. J Clin Invest, 1994,94:1320 - 1327
  • 6Bromberg ME, Sundaram R, Homer R J, et al. Role of tissue factor in metastasis: functions of the cytoplasmic and extracellular domains of the molecule [ J ]. Thromb Haemost, 1999,82:88 - 92
  • 7Taniguchi T, Kakkar AK, Tuddenham EG, et al. Enhanced expression of urokinase receptor induced through the tissue factor-factor Ⅵ-Ia pathway in human pancreatic cancer[ J ]. Cancer Res, 1998,58:4461 -4467
  • 8Ott I, Fischer EG, Miyagi Y, et al. A role for tissue factor in cell adhesion and migration mediated by interaction with actin-binding protein 280[J]. J Cell Biol, 1998,140:1241 - 1253
  • 9Camerer E,Rottingen JA, Gjernes E, et al. Coagulation factors Ⅶa and Xa induce cell signaling leading to up-regulation of the egr-1 gene[ J]. J Biol Chem, 1999,274: 32225 - 32233
  • 10Esteve PO, Chicoine E, Robledo O, et al. Protein kinase C-zeta regulates transcription of the matrix metalloproteinase-9 gene induced by IL-1 and TNF-alpha in glioma cells via NF-kappa B [ J ]. J Biol Chem,2002,277:35150 - 35155

共引文献19

同被引文献54

  • 1申哲洙,顾晋,赵威,张志谦.尿液中MMP-2、MMP-9及MMP-9/NGAL复合物的表达在乳腺癌筛查中的意义[J].首都医科大学学报,2008,29(3):395-398. 被引量:4
  • 2明洁,黄韬,田元,张景辉.外周血CK19、MMP-9和MDR1水平评定体外药敏的价值[J].实用癌症杂志,2006,21(5):461-463. 被引量:1
  • 3Pleshko RI. The morphofunctional prerequisites for the development of ex- udative otitis media in the children presenting with chronic adenoiditis. Vestn Otorinolaringol. 2014.39-41.
  • 4金晓昌,叶武坤.乳腺癌新辅助化疗后行前哨淋巴结活检47例分析.医药前沿,2011,1:129—130.
  • 5Hashmi AA. Distribution of Ki67 Proliferative Indices among WHO Sub- types of Non-Hodgkin' s Lymphoma: Association with other Clinical Pa- rameters. Asian Pac J Cancer Prey,2014,15:8759-8763.
  • 6Paydas S. Expression of p53, Ki67, epidermal growth factor receptor, transforming growth-factor , and p21 in primary and secondary hyper- parathyroidism. Indian J Endocrinol Metab,2014,18:826-830.
  • 7Chia CY, Kumari U, Casey PJ. Breast cancer cell invasion mediated by Gotl2 signaling involves expression of interleukins-6 and -8, and matrix metalloproteinase-2[ J]. J Mol Signal, 2014, 9: 6.
  • 8Batra J, Robinson J, Mehner C, et al. PEGylation extends circulation half-life while preserving in vitro and in vivo activity of tissue inhibitor of metalloproteinases-I ( TIMP-I ) [ J ]. PLoS One, 2012, 7 ( 11 ) : e50028.
  • 9Martin MD, Carter K J, Jean-Philippe SR, et al. Effect of ablation or inhibition of stromal matrix metalloproteinase-9 on lung metastasis in a breast cancer model is dependent on genetic background [ J]. Cancer Res, 2008, 68 ( 15 ) : 625145259.
  • 10Mehner C, Hoekla A, Miller E, et al. Tumor cell-produced matrix metallo proteinase-9 (MMP-9) drives malignant progression and metastasis of basal-like triple negative breast cancer[J]. Oncotarget, 2014, 5 (9) : 2736-2749.

引证文献3

二级引证文献9

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