Cysteine Dioxygenase 1 Is a Tumor Suppressor Gene Silenced by Promoter Methylation in Multiple Human Cancers

被引:105
作者
Brait, Mariana [1 ,2 ]
Ling, Shizhang [3 ]
Nagpal, Jatin K. [1 ]
Chang, Xiaofei [1 ]
Park, Hannah Lui [4 ]
Lee, Juna [1 ]
Okamura, Jun [1 ]
Yamashita, Keishi [5 ]
Sidransky, David [1 ]
Kim, Myoung Sook [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol, Head & Neck Canc Res Div, Baltimore, MD 21205 USA
[2] Brazilian Natl Canc Inst, Inst Nacl Canc INCA, Rio De Janeiro, Brazil
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[4] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
[5] Kitasato Univ Hosp, Dept Surg, Sagamihara, Kanagawa, Japan
来源
PLOS ONE | 2012年 / 7卷 / 09期
关键词
CYSTATHIONINE BETA-SYNTHASE; TISSUE-SPECIFIC EXPRESSION; SQUAMOUS-CELL CARCINOMA; HYDROGEN-SULFIDE; ETHYLMALONIC ENCEPHALOPATHY; COLON-CANCER; STRUCTURAL ORGANIZATION; RHEUMATOID-ARTHRITIS; COLORECTAL-CARCINOMA; OXIDATIVE STRESS;
D O I
10.1371/journal.pone.0044951
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human cysteine dioxygenase 1 (CDO1) gene is a non-heme structured, iron-containing metalloenzyme involved in the conversion of cysteine to cysteine sulfinate, and plays a key role in taurine biosynthesis. In our search for novel methylated gene promoters, we have analyzed differential RNA expression profiles of colorectal cancer (CRC) cell lines with or without treatment of 5-aza-2'-deoxycytidine. Among the genes identified, the CDO1 promoter was found to be differentially methylated in primary CRC tissues with high frequency compared to normal colon tissues. In addition, a statistically significant difference in the frequency of CDO1 promoter methylation was observed between primary normal and tumor tissues derived from breast, esophagus, lung, bladder and stomach. Downregulation of CDO1 mRNA and protein levels were observed in cancer cell lines and tumors derived from these tissue types. Expression of CDO1 was tightly controlled by promoter methylation, suggesting that promoter methylation and silencing of CDO1 may be a common event in human carcinogenesis. Moreover, forced expression of full-length CDO1 in human cancer cells markedly decreased the tumor cell growth in an in vitro cell culture and/or an in vivo mouse model, whereas knockdown of CDO1 increased cell growth in culture. Our data implicate CDO1 as a novel tumor suppressor gene and a potentially valuable molecular marker for human cancer.
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页数:19
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