Critical Function for Nuclear Envelope Protein TMEM209 in Human Pulmonary Carcinogenesis

被引:31
作者
Fujitomo, Takashi
Daigo, Yataro [2 ,3 ]
Matsuda, Koichi
Ueda, Koji [4 ]
Nakamura, Yusuke [1 ]
机构
[1] Univ Tokyo, Mol Med Lab, Ctr Human Genome, Inst Med Sci,Minato Ku, Tokyo 1088639, Japan
[2] Shiga Univ Med Sci, Dept Med Oncol, Otsu, Shiga 52021, Japan
[3] Shiga Univ Med Sci, Ctr Canc, Otsu, Shiga 52021, Japan
[4] RIKEN, Lab Biomarker Dev, Ctr Genom Med, Yokohama, Kanagawa, Japan
关键词
CELL LUNG-CANCER; THERAPEUTIC TARGET; PROGNOSTIC BIOMARKER; EXPRESSION PROFILES; TESTIS ANTIGEN; TRANSCRIPTION FACTOR; BINDING PROTEIN-1; ACTIVATION; IDENTIFICATION; COMPLEX;
D O I
10.1158/0008-5472.CAN-12-0159
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapeutic targets for more effective and less toxic treatments of lung cancer remain important. Here we report the identification of the integral nuclear envelope protein TMEM209 as a critical driver of human lung cancer growth and survival. TMEM209 expression was normally limited to testis, but we found that it was widely expressed in lung cancer, in which it localized to the nuclear envelope, Golgi apparatus, and the cytoplasm of lung cancer cells. Ectopic overexpression of TMEM209 promoted cell growth, whereas TMEM209 attenuation was sufficient to block growth. Mass spectrometric analysis identified the nucleoporin protein NUP205 as a TMEM209-interacting protein, stabilizing NUP205 and increasing the level of c-Myc in the nucleus. Taken together, our findings indicate that TMEM209 overexpression and TMEM209-NUP205 interaction are critical drivers of lung cancer proliferation, suggesting a promising new target for lung cancer therapy. Cancer Res; 72( 16); 4110-8. (C) 2012 AACR.
引用
收藏
页码:4110 / 4118
页数:9
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