Apoptosis signal-regulating kinase 1 and cyclin D1 compose a positive feedback loop contributing to tumor growth in gastric cancer

被引:88
作者
Hayakawa, Yoku [1 ]
Hirata, Yoshihiro [1 ]
Nakagawa, Hayato [1 ]
Sakamoto, Kei [2 ]
Hikiba, Yohko [2 ]
Kinoshita, Hiroto [1 ]
Nakata, Wachiko [1 ]
Takahashi, Ryota [1 ]
Tateishi, Keisuke [1 ]
Tada, Motohisa [3 ]
Akanuma, Masao
Yoshida, Haruhiko [1 ]
Takeda, Kohsuke [4 ]
Ichijo, Hidenori [4 ]
Omata, Masao [1 ,2 ]
Maeda, Shin [1 ,5 ]
Koike, Kazuhiko [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Tokyo 1138655, Japan
[2] Asahi Life Fdn, Inst Adult Dis, Div Gastroenterol, Tokyo 1000005, Japan
[3] Chiba Univ, Grad Sch Med, Dept Med & Clin Oncol, Chiba 2600856, Japan
[4] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Cell Signaling, Tokyo 1130033, Japan
[5] Yokohama City Univ, Dept Gastroenterol, Yokohama, Kanagawa 2360004, Japan
关键词
JNK; c-Jun; ACTIVATED PROTEIN-KINASES; RETINOBLASTOMA PROTEIN; FACTOR RECEPTOR; BETA-CATENIN; FACTOR-ALPHA; ASK1; MICE; CELLS; EXPRESSION; PROMOTER;
D O I
10.1073/pnas.1011418108
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Mitogen-activated protein kinase (MAPK) pathways regulate multiple cellular functions and are highly active in many types of human cancers. Apoptosis signal-regulating kinase 1 (ASK1) is an upstream MAPK involved in apoptosis, inflammation, and carcinogenesis. This study investigated the role of ASK1 in the development of gastric cancer. In human gastric cancer specimens, we observed increased ASK1 expression, compared to nontumor epithelium. Using a chemically induced murine gastric tumorigenesis model, we observed increased tumor ASK1 expression, and ASK1 knockout mice had both fewer and smaller tumors than wild-type (WT) mice. ASK1 siRNA inhibited cell proliferation through the accumulation of cells in G1 phase of the cell cycle, and reduced cyclin D1 expression in gastric cancer cells, whereas these effects were uncommon in other cancer cells. ASK1 overexpression induced the transcription of cyclin D1, through AP-1 activation, and ASK1 levels were regulated by cyclin D1, via the Rb-E2F pathway. Exogenous ASK1 induced cyclin D1 expression, followed by elevated expression of endogenous ASK1. These results indicate an autoregulatory mechanism of ASK1 in the development of gastric cancer. Targeting this positive feedback loop, ASK1 may present a potential therapeutic target for the treatment of advanced gastric cancer.
引用
收藏
页码:780 / 785
页数:6
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