RET finger protein expression is associated with prognosis in lung cancer with epidermal growth factor receptor mutations

被引:27
作者
Iwakoshi, Akari
Murakumo, Yoshiki [1 ]
Kato, Takuya
Kitamura, Aya
Mii, Shinji
Saito, Shoji [2 ]
Yatabe, Yasushi [3 ]
Takahashi, Masahide [4 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Pathol, Showa Ku, Nagoya, Aichi 4668850, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Internal Med, Nagoya, Aichi 4668850, Japan
[3] Nagoya Univ, Grad Sch Med, Aichi Canc Ctr, Dept Pathol & Mol Diagnost, Nagoya, Aichi 4668850, Japan
[4] Nagoya Univ, Grad Sch Med, Ctr Neurol Dis & Canc, Div Mol Pathol, Nagoya, Aichi 4668850, Japan
关键词
epidermal growth factor receptor mutation; immunohistochemistry; lung cancer; RET finger protein; thyroid transcription factor 1; GENE-EXPRESSION; ADENOCARCINOMA; CLASSIFICATION; MI-2-BETA; ENHANCER;
D O I
10.1111/j.1440-1827.2012.02797.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The RET finger protein (RFP) is a transcription factor belonging to the TRIM (tripartite motif) superfamily of proteins. RFP is expressed in a variety of human and rodent tumor cell lines and in several kinds of human cancer. Expression of RFP is associated with prognosis of colon and endometrial cancers. In the present study, we evaluated the expression of RFP in lung cancer and assessed its clinical significance. Tissue microarrays were constructed from 108 cases of lung cancer, and the sections were analyzed for RFP expression by immunohistochemistry. RFP expression was detected in the nucleus in 66.7% of lung cancer tissues examined. RFP expression was statistically significantly associated with thyroid transcription factor 1 (TTF-1) expression (P= 0.028). However, no significant association was observed between RFP expression and other clinicopathological or genetic factors, including epidermal growth factor receptor (EGFR) mutations. Interestingly, we found that RFP expression correlated with poor prognosis in patients with EGFR mutations (P= 0.032). Our results suggest that RFP has a role in mutated EGFR signaling and that RFP status may be a prognostic factor for lung cancer with EGFR mutations.
引用
收藏
页码:324 / 330
页数:7
相关论文
共 28 条
[1]   Gene-expression profiles predict survival of patients with lung adenocarcinoma [J].
Beer, DG ;
Kardia, SLR ;
Huang, CC ;
Giordano, TJ ;
Levin, AM ;
Misek, DE ;
Lin, L ;
Chen, GA ;
Gharib, TG ;
Thomas, DG ;
Lizyness, ML ;
Kuick, R ;
Hayasaka, S ;
Taylor, JMG ;
Iannettoni, MD ;
Orringer, MB ;
Hanash, S .
NATURE MEDICINE, 2002, 8 (08) :816-824
[2]   Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses [J].
Bhattacharjee, A ;
Richards, WG ;
Staunton, J ;
Li, C ;
Monti, S ;
Vasa, P ;
Ladd, C ;
Beheshti, J ;
Bueno, R ;
Gillette, M ;
Loda, M ;
Weber, G ;
Mark, EJ ;
Lander, ES ;
Wong, W ;
Johnson, BE ;
Golub, TR ;
Sugarbaker, DJ ;
Meyerson, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13790-13795
[3]   Diversity of gene expression in adenocarcinoma of the lung [J].
Garber, ME ;
Troyanskaya, OG ;
Schluens, K ;
Petersen, S ;
Thaesler, Z ;
Pacyna-Gengelbach, M ;
van de Rijn, M ;
Rosen, GD ;
Perou, CM ;
Whyte, RI ;
Altman, RB ;
Brown, PO ;
Botstein, D ;
Petersen, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13784-13789
[4]   Characterization of the HDAC1 Complex That Regulates the Sensitivity of Cancer Cells to Oxidative Stress [J].
Kato, Takuya ;
Shimono, Yohei ;
Hasegawa, Masaki ;
Jijiwa, Mayumi ;
Enomoto, Atsushi ;
Asai, Naoya ;
Murakumo, Yoshiki ;
Takahashi, Masahide .
CANCER RESEARCH, 2009, 69 (08) :3597-3604
[5]   The T/ebp null mouse thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary [J].
Kimura, S ;
Hara, Y ;
Pineau, T ;
FernandezSalguero, P ;
Fox, CH ;
Ward, JM ;
Gonzalez, FJ .
GENES & DEVELOPMENT, 1996, 10 (01) :60-69
[6]   Mutations of the epidermal growth factor receptor gene in lung cancer:: Biological and clinical implications [J].
Kosaka, T ;
Yatabe, Y ;
Endoh, H ;
Kuwano, H ;
Takahashi, T ;
Mitsudomi, T .
CANCER RESEARCH, 2004, 64 (24) :8919-8923
[7]   Selective ablation of retinoblastoma protein function by the RET finger protein [J].
Krützfeldt, M ;
Ellis, M ;
Weekes, DB ;
Bull, JJ ;
Eilers, M ;
Vivanco, MDM ;
Sellers, WR ;
Mittnacht, S .
MOLECULAR CELL, 2005, 18 (02) :213-224
[8]   Gefitinib or Chemotherapy for Non-Small-Cell Lung Cancer with Mutated EGFR. [J].
Maemondo, Makoto ;
Inoue, Akira ;
Kobayashi, Kunihiko ;
Sugawara, Shunichi ;
Oizumi, Satoshi ;
Isobe, Hiroshi ;
Gemma, Akihiko ;
Harada, Masao ;
Yoshizawa, Hirohisa ;
Kinoshita, Ichiro ;
Fujita, Yuka ;
Okinaga, Shoji ;
Hirano, Haruto ;
Yoshimori, Kozo ;
Harada, Toshiyuki ;
Ogura, Takashi ;
Ando, Masahiro ;
Miyazawa, Hitoshi ;
Tanaka, Tomoaki ;
Saijo, Yasuo ;
Hagiwara, Koichi ;
Morita, Satoshi ;
Nukiwa, Toshihiro .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (25) :2380-2388
[9]   Tripartite-motif proteins and innate immune regulation [J].
McNab, Finlay W. ;
Rajsbaum, Ricardo ;
Stoye, Jonathan P. ;
O'Garra, Anne .
CURRENT OPINION IN IMMUNOLOGY, 2011, 23 (01) :46-56
[10]   Gefitinib versus cisplatin plus docetaxel in patients with non-small-cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomised phase 3 trial [J].
Mitsudomi, Tetsuya ;
Morita, Satoshi ;
Yatabe, Yasushi ;
Negoro, Shunichi ;
Okamoto, Isamu ;
Tsurutani, Junji ;
Seto, Takashi ;
Satouchi, Miyako ;
Tada, Hirohito ;
Hirashima, Tomonori ;
Asami, Kazuhiro ;
Katakami, Nobuyuki ;
Takada, Minoru ;
Yoshioka, Hiroshige ;
Shibata, Kazuhiko ;
Kudoh, Shinzoh ;
Shimizu, Eiji ;
Saito, Hiroshi ;
Toyooka, Shinichi ;
Nakagawa, Kazuhiko ;
Fukuoka, Masahiro .
LANCET ONCOLOGY, 2010, 11 (02) :121-128