期刊文献+

非小细胞肺癌中RECK和MMP-9的表达及其临床意义 被引量:3

Expression of RECK and MMP-9 in non-small-cell lung carcinoma and its clinical significance
在线阅读 下载PDF
导出
摘要 目的观察基序逆向诱导半胱氨酸丰富蛋白(reversion inducing cysteine rich protein with kazal motifs,RECK)及基质金属蛋白酶-9(matrix metalproteinase-9,MMP-9)在非小细胞肺癌(non-small-cell lung carcinoma,NSCLC)组织中的表达情况,探讨其表达与临床病理特征的关系。方法选取我院临床病理资料齐全的NSCLC标本66例,并选取30例炎性假瘤作为对照组。采用免疫组化法检测组织中RECK和MMP-9的表达情况,并进行统计学分析。结果RECK和MMP-9在NSCLC组织中的阳性表达率分别为40.9%和75.6%,与炎性假瘤对照组相比,两者差异均具有统计学意义(P<0.05)。RECK与MMP-9的表达与患者原发肿瘤大小,病理学类型,分化程度无关(P>0.05)。临床分期为Ⅰ~Ⅱ期组RECK阳性率高于Ⅲ~Ⅳ期(P<0.05),无淋巴结转组阳性率高于转移组(P<0.05),而MMP-9与之相反。NSCLC组织中RECK与MMP-9的表达呈负相关(P<0.05)。结论肺小细胞癌组织中RECK表达降低,MMP-9增高,两者联合检测有望成为评估临床预后的重要指标。 Objective To study the expression of RECK and MMP-9 in non-small-cell lung carcinoma (NSCLC) and analyze the clinical significance between RECK and MMP-9 expression. Methods 66 cases of NSCLS specimens and with complete clinical information were selected and 30 cases of inflammatory pseudotumor were used as control group. The expression of RECK and MMP-9 were detected by immunohistochemical method, then statistical analysis was performed. Results The positive rate of RECK and MMP-9 in NSCLC were 40.9% and 75.6%, repectively, they were significant difference compare with inflammatory pseudotumor group. There were no significant correlation was found with tumor size, pathological type and tumor differentiation (P 〉 0.05). The positive rate of RECK in I - II stage was higher than III- IV stage, and the rate of lymph nodes metastases was higher than that without lymph nodes metastases (P 〈 0.05), but it was opposite for MMP-9. The expression of RECK was negatively correlated with MMP-9 (P 〈 0.05). Conclusion RECK is lowly expressed in NSCLC, and MMP-9 is upgraded. They may be served as an important marker for evaluation of clinical prognosis.
出处 《中国医药导报》 CAS 2012年第12期46-48,共3页 China Medical Herald
关键词 非小细胞肺癌 基序逆向诱导半胱氨酸丰富蛋白 基质金属蛋白酶-9 Non-small-cell lung carcinoma RECK Matrix metalloproteinase-9
作者简介 通讯作者
  • 相关文献

参考文献11

  • 1Cagle PT,Allen TC,Dacic S. Revolution in lung cancer:new challenges for the surgical pathologist[J].Archives of Pathology and Laboratory Medicine,2011,(01):110-116.
  • 2Blanco M,Garcia-Fontan E,Rios J. Pulmonar collision tumor:metastatic adenoid cystic carcinoma and lungadenocarcinoma[J].Rev Port Pneumol,2012,(01):42-45.
  • 3Noda M,Takahashi C,Matsuzaki T. What we learn from transformation suppressor genes:lessons from RECK[J].FUTURE ONCOLOGY,2010,(07):1105-1116.
  • 4Zheng S,Chang Y,Hodges KB. Expression of KISS1 and MMP-9 in non-small cell lung cancer and their relations to metastasis and survival[J].Anticancer Research,2010,(03):713-718.
  • 5Stenvold H,Donnem T,Andersen S. Overexpression of matrix metalloproteinase-7 and -9 in NSCLC tumor and stromalcells:correlation with a favorable clinical outcome[J].Lung Cancer,2012,(02):235-241.
  • 6Sienel W,Hellers J,Morresi-Hauf A. Prognostic impact of matrix metalloproteinase-9 in operable non-small cell lung cancer[J].International Journal of Cancer,2003,(05):647-651.
  • 7Zheng S,Chang Y,Hodges KB. Expression of KISS1 and MMP-9 in non-small cell lung cancer and their relationsto metastasis and survival[J].Anticancer Research,2010,(03):713-718.
  • 8Shao W,Wang W,Xiong XG. Prognostic impact of MMP-2 and MMP-9 expression in pathologic stage IA non-small cell lung cancer[J].Journal of Surgical Oncology,2011,(07):841-846.
  • 9Chang HC,Cho CY,Hung WC. Downregulation of RECK by promoter methylation correlates with lymph node metastasis in non-small cell lung cancer[J].Cancer Science,2007,(02):169-173.
  • 10Pesta M,Kulda V,Topolcan O. Significance of methylation status and the expression of RECK mRNA in lung tissue of patients with NSCLC[J].Anticancer Research,2009,(11):4535-4539.

同被引文献33

  • 1王文武,戴西湖,欧阳学农.川芎嗪对小鼠Lewis肺癌的治疗作用[J].中国临床药理学与治疗学,2005,10(4):421-423. 被引量:10
  • 2梁爱群.川芎嗪的药理及机理研究[J].时珍国医国药,2005,16(6):532-533. 被引量:86
  • 3Teramoto K,Asada Y,Ozaki Y,et al. A phase II study of docetaxel plus nedaplatin in patients with metastatic non- small-cell lung cancer [J]. Cancer Chemotherapy and Pharmacology,2012,70(4) :531-537.
  • 4Kajiura S,Hosokawa A,Yoshita H,et al. Phase I study of Docetaxel plus Nedaplatin in patients with metastatic or recurrent esophageal squamous cell carcinoma after Cis- platin plus 5-Fluorouracil treatment [J]. American Journal of Clinical Oncology ,2013, (2) :19-20.
  • 5Sugiyama T,Hirose T,Nakashima M,et al. Evaluation of the efficacy and safety of the combination of gemcitabine and nedaplatin for elderly patients with advanced non- small-cell lung cancer [J]. Oncology, 2011,81 (3 -4) : 273- 280.
  • 6Naito Y,Kubota K,Ohmatsu H,et al. Phase II study of nedaplatin and docetaxel in patients with advanced squa- mous cell carcinoma of the lung [J]. Annals of Oncology, 2011,22(11 ) :2471-2475.
  • 7Oshita F,Ohe M,Honda T,et al. Phase II study of nedaplatin and irinotecan with concurrent thoracic radiotherapy in pa- tients with locally advanced non-small-cell lung cancer [J]. British Journal of Cancer,2010,103(9) :1325-1330.
  • 8Takimoto T,Nakabori T,Osa A, et al. Tubular nephrotoxicity induced by docetaxel in non-small-cell lung cancer patients [J]. International Journal of Clinical Oncology, 2012,17(4) :395-398.
  • 9Xue C,Hu Z,Jiang W,et al. National survey of the medical treatment status for non-small cell lung cancer(NSCLC) in China [J]. Lung Cancer,2012,77(2):371-375.
  • 10Lin Q,Meng FJ,Liu Y,et al. Phase II trial of capecitabine combined with docetaxel in previously treated patients with non-small cell lung cancer:a randomized controlled study [J]. Oncology Letters, 2012,3 (4) :761-766.

引证文献3

二级引证文献26

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