Promoter methylation of leukemia inhibitory factor receptor gene in colorectal carcinoma

被引:28
作者
Cho, Yong Gu [1 ]
Chang, Xiaofei [1 ]
Park, Il-Seok [2 ]
Yamashita, Keishi
Shao, Chunbo [1 ,3 ]
Ha, Patrick K. [1 ]
Pai, Sara I. [1 ]
Sidransky, David [1 ]
Kim, Myoung Sook [1 ]
机构
[1] Johns Hopkins Univ, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21231 USA
[2] Hallym Univ, Coll Med, Dept Otolaryngol Head & Neck Surg, Ilsong Mem Inst Head & Neck Canc, Seoul 150030, South Korea
[3] Kitasato Univ Hosp, Dept Surg, Kanagawa 2288555, Japan
关键词
leukemia inhibitory factor receptor; methylation; colorectal carcinoma; TUMOR-SUPPRESSIVE ACTIVITY; ONCOSTATIN-M-RECEPTOR; DNA METHYLATION; TARGETED DISRUPTION; SIGNAL TRANSDUCER; EPITHELIAL-CELLS; LUNG-CANCER; INTERLEUKIN-6; EXPRESSION; CYTOKINES;
D O I
10.3892/ijo.2011.1050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant methylation of gene promoters and corresponding loss of gene expression plays a critical role in the initiation and progression of colorectal cancer. An IL-6-type cytokine receptor, leukemia inhibitory factor receptor (LIFR), is a component of cell-surface receptor complexes for multifunctional cytokines such as LIP. Herein, we report that LIFR is methylated in human colon cancer. LIFR promoter was methylated in primary tumor tissues with high frequency (65%, 52/80). Quantitative rnethylation-specific PCR (TaqMan-MSP) demonstrated differential promoter methylation of LIFR in primary colorectal cancer tissues as compared to normal colon tissues (5%, 4/80). LIFR methylation was not detectable in 13 normal colon mucosa samples obtained from patients without cancer. The mRNA expression of LIFR was significantly down-regulated in colon cancer tissues as compared to corresponding normal tissues. A strong expression of LIFR protein was observed in all non-malignant normal and adjacent normal colon mucosa tissues whereas down-regulated LIFR protein expression was observed in primary tumors. These results demonstrate that cancer-specific methylation and a specific decrease of LIFR expression are a common inactivation event in colon cancer development.
引用
收藏
页码:337 / 344
页数:8
相关论文
共 36 条
[21]   Transformation of human bronchial epithelial cells alters responsiveness to inflammatory cytokines [J].
Loewen, GM ;
Tracy, E ;
Blanchard, F ;
Tan, DF ;
Yu, JH ;
Raza, S ;
Matsui, SI ;
Baumann, H .
BMC CANCER, 2005, 5 (1)
[22]   PGP9.5 promoter methylation is an independent prognostic factor for esophageal squamous cell carcinoma [J].
Mandelker, DL ;
Yamashita, K ;
Tokumaru, Y ;
Mimori, K ;
Howard, DL ;
Tanaka, Y ;
Carvalho, AL ;
Jiang, WW ;
Park, HL ;
Kim, MS ;
Osada, M ;
Mori, M ;
Sidransky, D .
CANCER RESEARCH, 2005, 65 (11) :4963-4968
[23]   Dual oncostatin M (OSM) receptors - Cloning and characterization of an alternative signaling subunit conferring OSM-specific receptor activation [J].
Mosley, B ;
DeImus, C ;
Friend, D ;
Boiani, N ;
Thoma, B ;
Park, LS ;
Cosman, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) :32635-32643
[24]   IDENTIFICATION OF A MAJOR GROWTH-FACTOR FOR AIDS KAPOSIS-SARCOMA CELLS AS ONCOSTATIN-M [J].
NAIR, BC ;
DEVICO, AL ;
NAKAMURA, S ;
COPELAND, TD ;
CHEN, Y ;
PATEL, A ;
ONEIL, T ;
OROSZLAN, S ;
GALLO, RC ;
SARNGADHARAN, MG .
SCIENCE, 1992, 255 (5050) :1430-1432
[25]   Leukemia inhibitory factor receptor (LIFR) is detected as a novel suppressor gene of hepatocellular carcinoma using double-combination array [J].
Okamura, Yukiyasu ;
Nomoto, Shuji ;
Kanda, Mitsuro ;
Li, Qiyong ;
Nishikawa, Yoko ;
Sugimoto, Hiroyuki ;
Kanazumi, Naohito ;
Takeda, Shin ;
Nakao, Akimasa .
CANCER LETTERS, 2010, 289 (02) :170-177
[26]  
Palmisano WA, 2000, CANCER RES, V60, P5954
[27]   Expression of interleukin-6, leukemia inhibitory factor and their receptors by colonic epithelium and pericryptal fibroblasts [J].
Rockman, SP ;
Demmler, K ;
Roczo, N ;
Cosgriff, A ;
Phillips, WA ;
Thomas, RJS ;
Whitehead, RH .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2001, 16 (09) :991-1000
[28]   Immunohistochemical analysis of the IL-6 family of cytokines and their receptors in benign, hyperplasic, and malignant human prostate [J].
Royuela, M ;
Ricote, M ;
Parsons, MS ;
Garcia-Tuñón, I ;
Paniagua, R ;
De Miguel, MP .
JOURNAL OF PATHOLOGY, 2004, 202 (01) :41-49
[29]   Emerging molecular markers of cancer [J].
Sidransky, D .
NATURE REVIEWS CANCER, 2002, 2 (03) :210-219
[30]   Structural and functional studies on the leukemia inhibitory factor receptor (LIF-R): Gene and soluble form of LIF-R, and cytoplasmic domain of LIF-R required for differentiation and growth arrest of myeloid leukemic cells [J].
Tomida, M .
LEUKEMIA & LYMPHOMA, 2000, 37 (5-6) :517-525