The Arkadia-ESRP2 axis suppresses tumor progression: analyses in clear-cell renal cell carcinoma
被引:0
|
作者:
A Mizutani
论文数: 0引用数: 0
h-index: 0
机构:Graduate School of Medicine,Department of Molecular Pathology
A Mizutani
D Koinuma
论文数: 0引用数: 0
h-index: 0
机构:Graduate School of Medicine,Department of Molecular Pathology
D Koinuma
H Seimiya
论文数: 0引用数: 0
h-index: 0
机构:Graduate School of Medicine,Department of Molecular Pathology
H Seimiya
K Miyazono
论文数: 0引用数: 0
h-index: 0
机构:Graduate School of Medicine,Department of Molecular Pathology
K Miyazono
机构:
[1] Graduate School of Medicine,Department of Molecular Pathology
[2] The University of Tokyo,Division of Molecular Biotherapy
[3] Cancer Chemotherapy Center,undefined
[4] Japanese Foundation for Cancer Research,undefined
[5] Ariake,undefined
[6] Koto-ku,undefined
来源:
Oncogene
|
2016年
/
35卷
关键词:
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Tumor-specific alternative splicing is implicated in the progression of cancer, including clear-cell renal cell carcinoma (ccRCC). Using ccRCC RNA sequencing data from The Cancer Genome Atlas, we found that epithelial splicing regulatory protein 2 (ESRP2), one of the key regulators of alternative splicing in epithelial cells, is expressed in ccRCC. ESRP2 mRNA expression did not correlate with the overall survival rate of ccRCC patients, but the expression of some ESRP-target exons correlated with the good prognosis and with the expression of Arkadia (also known as RNF111) in ccRCC. Arkadia physically interacted with ESRP2, induced polyubiquitination and modulated its splicing function. Arkadia and ESRP2 suppressed ccRCC tumor growth in a coordinated manner. Lower expression of Arkadia correlated with advanced tumor stages and poor outcomes in ccRCC patients. This study thus reveals a novel tumor-suppressive role of the Arkadia-ESRP2 axis in ccRCC.
机构:
Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Japanese Fdn Canc Res, Div Mol Biotherapy, Ctr Canc Chemotherapy, Koto Ku, Tokyo, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Mizutani, A.
Koinuma, D.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Koinuma, D.
Seimiya, H.
论文数: 0引用数: 0
h-index: 0
机构:
Japanese Fdn Canc Res, Div Mol Biotherapy, Ctr Canc Chemotherapy, Koto Ku, Tokyo, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Seimiya, H.
Miyazono, K.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
机构:
Mem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA
Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, 1275 York Ave, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA
Vuong, Lynda
Kotecha, Ritesh R.
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA
Kotecha, Ritesh R.
Voss, Martin H.
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA
Voss, Martin H.
Hakimi, A. Ari
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA
Mem Sloan Kettering Canc Ctr, Dept Urol, 1275 York Ave, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Immunogen & Precis Oncol Platform, 1275 York Ave, New York, NY 10021 USA