Senescence marker protein 30 (SMP30)/regucalcin (RGN) expression decreases with aging, acute liver injuries and tumors in zebrafish

被引:29
作者
Fujisawa, Koichi [2 ]
Terai, Shuji [1 ]
Hirose, Yoshikazu [1 ]
Takami, Taro [3 ]
Yamamoto, Naoki [1 ]
Sakaida, Isao [1 ,2 ]
机构
[1] Yamaguchi Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, Ube, Yamaguchi 7558505, Japan
[2] Yamaguchi Univ, Sch Med, Ctr Reparat Med, Ube, Yamaguchi 7558505, Japan
[3] Yamaguchi Univ, Div Lab, Ube, Yamaguchi 7558505, Japan
基金
日本学术振兴会;
关键词
Zebrafish; Liver tumors; Aging; Senescence marker protein 30 (SMP30); Regucalcin; HEPATOMA H4-II-E CELLS; REGUCALCIN MESSENGER-RNA; RAT-LIVER; GENE-EXPRESSION; MODEL; OVEREXPRESSION; PROLIFERATION; REGENERATION; CARCINOMA; GROWTH;
D O I
10.1016/j.bbrc.2011.09.067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Senescence marker protein 30 (SMP30)/regucalcin (RGN) is known to be related to aging, hepatocyte proliferation and tumorigenesis. However, expression and function of non-mammalian SMP30/RGN is poorly understood. We found that zebrafish SMP30/RGN mRNA expression decreases with aging, partial hepatectomy and thioacetamide-induced acute liver injury. SMP30/RGN expression was also greatly decreased in a zebrafish liver cell line. In addition, we induced liver tumors in adult zebrafish by administering diethylnitrosamine. Decreased expression was observed in foci, hepatocellular carcinomas, cholangiocellular carcinomas and mixed tumors as compared to the surrounding area. We thus showed the importance of SMP30/RGN in liver proliferation and tumorigenesis. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:331 / 336
页数:6
相关论文
共 30 条
[1]
Gene expression profiling reveals the mechanism and pathophysiology of mouse liver regeneration [J].
Arai, M ;
Yokosuka, O ;
Chiba, T ;
Imazeki, F ;
Kato, M ;
Hashida, J ;
Ueda, Y ;
Sugano, S ;
Hashimoto, K ;
Saisho, H ;
Takiguchi, M ;
Seki, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29813-29818
[2]
Single dose intravenous thioacetamide administration as a model of acute liver damage in rats [J].
Chen, Tse-Min ;
Subeq, Yi-Maun ;
Lee, Ru-Ping ;
Chiou, Tzyy-Wen ;
Hsu, Bang-Gee .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2008, 89 (04) :223-231
[3]
Adenylate kinase isozyme 2 is essential for growth and development of Drosophila melanogaster [J].
Fujisawa, Koichi ;
Murakami, Ryutaro ;
Horiguchi, Taigo ;
Noma, Takafumi .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2009, 153 (01) :29-38
[4]
PURIFICATION OF SENESCENCE MARKER PROTEIN-30 (SMP30) AND ITS ANDROGEN-INDEPENDENT DECREASE WITH AGE IN THE RAT-LIVER [J].
FUJITA, T ;
UCHIDA, K ;
MARUYAMA, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1116 (02) :122-128
[5]
DERIVATION AND CHARACTERIZATION OF A ZEBRAFISH LIVER-CELL LINE [J].
GHOSH, C ;
ZHOU, YL ;
COLLODI, P .
CELL BIOLOGY AND TOXICOLOGY, 1994, 10 (03) :167-176
[6]
New waves of discovery: Modeling cancer in zebrafish [J].
Goessling, Wolfram ;
North, Trista E. ;
Zon, Leonard I. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (17) :2473-2479
[7]
Over-expression of Senescence Marker Protein-30 Decreases Reactive Oxygen Species in Human Hepatic Carcinoma Hep G2 Cells [J].
Handa, Setsuko ;
Maruyama, Naoki ;
Ishigami, Akihito .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2009, 32 (10) :1645-1648
[8]
SMP30 deficiency in mice causes an accumulation of neutral lipids and phospholipids in the liver and shortens the life span [J].
Ishigami, A ;
Kondo, Y ;
Nanba, R ;
Ohsawa, T ;
Handa, S ;
Kubo, S ;
Akita, M ;
Maruyama, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 315 (03) :575-580
[9]
Regulatory effects of senescence marker protein 30 on the proliferation of hepatocytes [J].
Ishigami, T ;
Fujita, T ;
Simbula, G ;
Columbano, A ;
Kikuchi, K ;
Ishigami, A ;
Shimosawa, T ;
Arakawa, Y ;
Maruyama, N .
PATHOLOGY INTERNATIONAL, 2001, 51 (07) :491-497
[10]
Overexpression of regucalcin suppresses cell death in cloned rat hepatoma H4-II-E cells induced by tumor necrosis factor-α or thapsigargin [J].
Izumi, T ;
Yamaguchi, M .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 92 (02) :296-306