Matrix metalloproteinase 12 is an independent prognostic factor predicting postoperative relapse of conventional renal cell carcinoma-a short report

被引:4
作者
Beres, Bence [1 ]
Yusenko, Maria [2 ]
Peterfi, Lehel [1 ]
Kovacs, Gyula [1 ,3 ]
Banyai, Daniel [1 ]
机构
[1] Univ Pecs, Sch Med, Dept Urol, Pecs, Hungary
[2] Univ Munster, Inst Biochem, Munster, Germany
[3] Ruprecht Karls Univ Heidelberg, Fac Med, Heidelberg, Germany
关键词
Conventional renal cell carcinoma; Sarcomatous renal cell carcinoma; MMP12; Immunohistochemistry; Prognosis; TUMOR; ANGIOSTATIN; EXPRESSION; GROWTH;
D O I
10.1007/s13402-021-00650-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Approximately 15% of clinically localised conventional renal cell carcinomas (cRCC) develop metastases within 5 years of follow-up. Sarcomatous cRCC is a highly malignant cancer of the kidney. The aim of our study was to identify biomarkers for estimating the postoperative progression of cRCCs. Methods Global microarray-based gene expression analysis of RCCs with and without sarcomatous changes revealed that a high MMP12 expression was associated with a sarcomatous histology. Additionally, we analysed MMP12 expression using a multi-tissue array comprising 736 cRCC patients without metastasis at the time of surgery. The median follow-up time was 66 +/- 29 months. Results Immunohistochemistry revealed MMP12 expression in 187 of 736 cRCCs with good follow-up data. Subsequent Kaplan-Meier analysis revealed that patients with MMP12 positive tumours exhibited a significantly shorter tumour-free survival (p < 0.001). In multivariate Cox regression analysis a weak to strong MMP12 expression indicated a 2.4-2.8 times higher risk of postoperative tumour relapse (p < 0.001; p < 0.003, respectively). Conclusions MMP12 may serve as a biomarker to estimate postoperative cRCC relapse and as a possible target for penfluridol therapy.
引用
收藏
页码:193 / 198
页数:6
相关论文
共 21 条
[1]  
Brierley JD, 2017, TNM classification of malignant Tumours
[2]   Epidemiology and risk factors for kidney cancer [J].
Chow, Wong-Ho ;
Dong, Linda M. ;
Devesa, Susan S. .
NATURE REVIEWS UROLOGY, 2010, 7 (05) :245-257
[3]   Sarcomatoid renal cell carcinoma is an example of epithelial-mesenchymal transition [J].
Conant, Joanna L. ;
Peng, Zhihua ;
Evans, Mark F. ;
Naud, Shelly ;
Cooper, Kumarasen .
JOURNAL OF CLINICAL PATHOLOGY, 2011, 64 (12) :1088-1092
[4]  
Cornelius LA, 1998, J IMMUNOL, V161, P6845
[5]   Matrix metalloproteinase 12 promotes tumor propagation in the lung [J].
Ella, Ezra ;
Harel, Yaniv ;
Abraham, Michal ;
Wald, Hanna ;
Benny, Ofra ;
Karsch-Bluman, Adi ;
Vincent, Dive ;
Laurent, Devel ;
Amir, Gail ;
Izhar, Uzi ;
Shapira, Oz M. ;
Yoon, David ;
Lee, Hyun-Sung ;
Sugarbaker, David J. ;
Burt, Bryan ;
Peled, Amnon ;
Wald, Ori .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2018, 155 (05) :2164-+
[6]   Matrix Metalloproteinases' Role in Tumor Microenvironment [J].
Gonzalez-Avila, Georgina ;
Sommer, Bettina ;
Armando Garcia-Hernandez, A. ;
Ramos, Carlos .
TUMOR MICROENVIRONMENT: EXTRACELLULAR MATRIX COMPONENTS - PT A, 2020, 1245 :97-131
[7]  
Gorrin-Rivas MJ, 2000, CLIN CANCER RES, V6, P1647
[8]   Blocking MMP-12-modulated epithelial-mesenchymal transition by repurposing penfluridol restrains lung adenocarcinoma metastasis via uPA/uPAR/TGF-β/Akt pathway [J].
Hung, Wen-Yueh ;
Lee, Wei-Jiunn ;
Cheng, Guo-Zhou ;
Tsai, Ching-Han ;
Yang, Yi-Chieh ;
Lai, Tsung-Ching ;
Chen, Ji-Qing ;
Chung, Chi-Li ;
Chang, Jer-Hwa ;
Chien, Ming-Hsien .
CELLULAR ONCOLOGY, 2021, 44 (05) :1087-1103
[9]   Matrix Metalloproteinases: Regulators of the Tumor Microenvironment [J].
Kessenbrock, Kai ;
Plaks, Vicki ;
Werb, Zena .
CELL, 2010, 141 (01) :52-67
[10]   Expression of matrix metalloproteinase-12 is correlated with extracapsular spread of tumor from nodes with metastasis in head and neck squamous cell carcinoma [J].
Kim, Jin Man ;
Kim, Hak Jun ;
Koo, Bon Seok ;
Rha, Ki Sang ;
Yoon, Yeo-Hoon .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2013, 270 (03) :1137-1142