MicroRNA-145 Targets the Metalloprotease ADAM17 and Is Suppressed in Renal Cell Carcinoma Patients

被引:98
作者
Doberstein, Kai [1 ]
Steinmeyer, Nico [1 ]
Hartmetz, Ann-Kathrin [1 ]
Eberhardt, Wolfgang [1 ]
Mittelbronn, Michel [2 ]
Harter, Patrick N. [2 ]
Juengel, Eva [3 ]
Blaheta, Roman [3 ]
Pfeilschifter, Josef [1 ]
Gutwein, Paul [1 ]
机构
[1] Goethe Univ Hosp, Pharmazentrum Frankfurt Zentrum Arzneimittelforsc, D-60590 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Inst Neurol, Edinger Inst, D-60054 Frankfurt, Germany
[3] Goethe Univ Hosp, Dept Urol, D-60590 Frankfurt, Germany
来源
NEOPLASIA | 2013年 / 15卷 / 02期
关键词
HUMAN BREAST-CANCER; EXPRESSION SIGNATURE; THERAPEUTIC TARGET; POSITIVE FEEDBACK; RNA INTERFERENCE; IN-VIVO; MIR-145; PROLIFERATION; DISINTEGRIN; OVARIAN;
D O I
10.1593/neo.121222
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A disintegrin and metalloproteinase 17 (ADAM17) is a metalloprotease that is overexpressed in many cancer types, including renal cancers. However, the regulatory mechanisms of ADAM17 in cancer development and progression are poorly understood. In the present work, we provide evidence using overexpression and inhibition of microRNA 145 (miR-145) that miR-145 negatively regulates ADAM17 expression. Furthermore, we show that ADAM17 negatively regulates miR-145 through tumor necrosis factor alpha, resulting in a reciprocal negative feedback loop. In this study, the expression of ADAM17 and miR-145 correlated negatively in renal cancer tumor tissues and cell lines, suggesting an important regulatory mechanism. Additionally, we showed that the regulation of ADAM17 is partly involved in the effects of miR-145 on proliferation and migration, whereas no involvement in chemosensitivity was observed. Importantly, in the healthy kidney, miR-145 was detected in different cell types including tubular cells, which are considered the origin of renal cancer. In renal cancer cell lines, miR-145 expression was strongly suppressed by methylation. In summary, miR-145 is downregulated in renal cancer patients, which leads to the up-regulation of ADAM17 in renal cancer. Importantly, miR-145 and ADAM17 are regulated in a reciprocal negative feedback loop.
引用
收藏
页码:218 / U153
页数:15
相关论文
共 65 条
  • [1] ADAM17 as a Therapeutic Target in Multiple Diseases
    Arribas, Joaquin
    Esselens, Cary
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2009, 15 (20) : 2319 - 2335
  • [2] Hsa-mir-145 is the top EWS-FLI1-repressed microRNA involved in a positive feedback loop in Ewing's sarcoma
    Ban, J.
    Jug, G.
    Mestdagh, P.
    Schwentner, R.
    Kauer, M.
    Aryee, D. N. T.
    Schaefer, K-L
    Nakatani, F.
    Scotlandi, K.
    Reiter, M.
    Strunk, D.
    Speleman, F.
    Vandesompele, J.
    Kovar, H.
    [J]. ONCOGENE, 2011, 30 (18) : 2173 - 2180
  • [3] Role of ADAM17 in the ectodomain shedding of TNF-α and its receptors by neutrophils and macrophages
    Bell, Jessica H.
    Herrera, Amy H.
    Li, Ying
    Walcheck, Bruce
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2007, 82 (01) : 173 - 176
  • [4] Up-regulated expression of ADAM17 in human colon carcinoma: co-expression with EGFR in neoplastic and endothelial cells
    Blanchot-Jossic, F
    Jarry, A
    Masson, D
    Bach-Ngohou, K
    Paineau, J
    Denis, MG
    Laboisse, CL
    Mosnier, JF
    [J]. JOURNAL OF PATHOLOGY, 2005, 207 (02) : 156 - 163
  • [5] Nephrectomy in metastatic renal cell carcinoma.
    Steven C. Campbell
    Robert C. Flanigan
    Joseph I. Clark
    [J]. Current Treatment Options in Oncology, 2003, 4 (5) : 363 - 372
  • [6] MicroRNA in Prostate, Bladder, and Kidney Cancer: A Systematic Review
    Catto, James W. F.
    Alcaraz, Antonio
    Bjartell, Anders S.
    White, Ralph De Vere
    Evans, Christopher P.
    Fussel, Susanne
    Hamdy, Freddie C.
    Kallioniemi, Olli
    Mengual, Lourdes
    Schlomm, Thorsten
    Visakorpi, Tapio
    [J]. EUROPEAN UROLOGY, 2011, 59 (05) : 671 - 681
  • [7] Real-time quantification of microRNAs by stem-loop RT-PCR
    Chen, CF
    Ridzon, DA
    Broomer, AJ
    Zhou, ZH
    Lee, DH
    Nguyen, JT
    Barbisin, M
    Xu, NL
    Mahuvakar, VR
    Andersen, MR
    Lao, KQ
    Livak, KJ
    Guegler, KJ
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 (20) : e179.1 - e179.9
  • [8] miRNA-145 inhibits non-small cell lung cancer cell proliferation by targeting c-Myc
    Chen, Zhe
    Zeng, Huazong
    Guo, Yong
    Liu, Pei
    Pan, Hui
    Deng, Anmei
    Hu, Jian
    [J]. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2010, 29
  • [9] MicroRNA-145, a Novel Smooth Muscle Cell Phenotypic Marker and Modulator, Controls Vascular Neointimal Lesion Formation
    Cheng, Yunhui
    Liu, Xiaojun
    Yang, Jian
    Lin, Ying
    Xu, Da-Zhong
    Lu, Qi
    Deitch, Edwin A.
    Huo, Yuqing
    Delphin, Ellise S.
    Zhang, Chunxiang
    [J]. CIRCULATION RESEARCH, 2009, 105 (02) : 158 - U113
  • [10] miR-145 and miR-133a function as tumour suppressors and directly regulate FSCN1 expression in bladder cancer
    Chiyomaru, T.
    Enokida, H.
    Tatarano, S.
    Kawahara, K.
    Uchida, Y.
    Nishiyama, K.
    Fujimura, L.
    Kikkawa, N.
    Seki, N.
    Nakagawa, M.
    [J]. BRITISH JOURNAL OF CANCER, 2010, 102 (05) : 883 - 891