Apoptosis inhibitor 5 (API-5; AAC-11; FIF) is upregulated in human carcinomas in vivo

被引:23
作者
Koci, Lenka
Chlebova, Katarina [2 ]
Hyzdalova, Martina
Hofmanova, Jirina [2 ]
Jira, Miroslav [3 ]
Kysela, Petr [3 ]
Kozubik, Alois [2 ]
Kala, Zdenek [3 ]
Krejci, Pavel [1 ,2 ]
机构
[1] Acad Sci Czech Republic, Inst Biophys, Dept Cytokinet, Vvi, CZ-61265 Brno, Czech Republic
[2] Masaryk Univ, Fac Sci, Inst Expt Biol, Dept Anim Physiol & Immunol, CS-61137 Brno, Czech Republic
[3] Masaryk Univ Hosp, Dept Surg, Brno, Czech Republic
关键词
apoptosis inhibitor 5; anti-apoptosis clone 11; carcinoma; human; apoptosis; magnetic bead selection; EXPRESSION; CELLS; GENE;
D O I
10.3892/ol.2012.593
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Apoptosis inhibitor 5 (API-5) is a 55 kDa nuclear protein with potent anti-apoptotic signaling in tumor cells in vitro. In this study, we analyzed the expression of the API-5 protein in vivo in a broad spectrum of human carcinomas, including those of the colon, lung, liver, kidney, pancreas, stomach and esophagus using tumor tissues obtained during tumor resection. The results showed significant upregulation of API-5 expression in biopsies of lung (23%, n=13) and colorectal tumors (33%, n=27) in comparison with biopsies from the adjacent normal tissue. Colon cancer biopsies were used to study the cell populations with an upregulated level of expression of API-5 more closely. Using a magnetic bead-based selection for the epithelial cell marker EpCAM, we purified epithelial cells from the tumor and control tissues and analyzed these cells for API-5 expression by western immunoblotting. We observed that EpCAM-positive tumor cells expressed API-5 in all three colorectal cancer cases tested, in contrast to the control EpCAM-positive and EpCAM-negative cells isolated from the control or tumor tissues. These data suggest that the expression of the API-5 protein is upregulated in tumor epithelial cells and may serve as a prognostic marker in colorectal cancer.
引用
收藏
页码:913 / 916
页数:4
相关论文
共 10 条
[1]   Phenotypic characterization of human colorectal cancer stem cells [J].
Dalerba, Piero ;
Dylla, Scott J. ;
Park, In-Kyung ;
Liu, Rui ;
Wang, Xinhao ;
Cho, Robert W. ;
Hoey, Timothy ;
Gurney, Austin ;
Huang, Emina H. ;
Simeone, Diane M. ;
Shelton, Andrew A. ;
Parmiani, Giorgio ;
Castelli, Chiara ;
Clarke, Michael F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (24) :10158-10163
[2]   AAC-11 overexpression induces invasion and protects cervical cancer cells from apoptosis [J].
Kim, JW ;
Cho, HS ;
Kim, JH ;
Hur, SY ;
Kim, TE ;
Lee, JM ;
Kim, IK ;
Namkoong, SE .
LABORATORY INVESTIGATION, 2000, 80 (04) :587-594
[3]   The antiapoptotic protein Api5 and its partner, high molecular weight FGF2, are up-regulated in B cell chronic lymphoid leukemia [J].
Krejci, Pavel ;
Pejchalova, Katerina ;
Rosenbloom, Barry E. ;
Rosenfelt, Fred P. ;
Tran, Elizabeth L. ;
Laurell, Henrik ;
Wilcox, William R. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2007, 82 (06) :1363-1364
[4]   Functional identification of Api5 as a suppressor of E2F-dependent apoptosis in vivo [J].
Morris, Erick J. ;
Michaud, William A. ;
Ji, Jun-Yuan ;
Moon, Nam-Sung ;
Rocco, James W. ;
Dyson, Nicholas J. .
PLOS GENETICS, 2006, 2 (11) :1834-1848
[5]  
PEKOW J, 2011, INFLAMM BOWEL D 0506
[6]   The antiapoptotic protein AAC-11 interacts with and regulates Acinus-mediated DNA fragmentation [J].
Rigou, Patricia ;
Piddubnyak, Valeria ;
Faye, Audrey ;
Rain, Jean-Christophe ;
Michel, Laurence ;
Calvo, Fabien ;
Poyet, Jean-Luc .
EMBO JOURNAL, 2009, 28 (11) :1576-1588
[7]   Expression of the antiapoptosis gene, AAC-11, as a prognosis marker in non-small cell lung cancer [J].
Sasaki, H ;
Moriyama, S ;
Yukiue, H ;
Kobayashi, Y ;
Nakashima, Y ;
Kaji, M ;
Fukai, I ;
Kiriyama, M ;
Yamakawa, Y ;
Fujii, Y .
LUNG CANCER, 2001, 34 (01) :53-57
[8]   Large-scale identification of mammalian proteins localized to nuclear sub-compartments [J].
Sutherland, HGE ;
Mumford, GK ;
Newton, K ;
Ford, LV ;
Farrall, R ;
Dellaire, G ;
Cáceres, JF ;
Bickmore, WA .
HUMAN MOLECULAR GENETICS, 2001, 10 (18) :1995-2011
[9]  
Tewari M, 1997, CANCER RES, V57, P4063
[10]  
Wang ZM, 2010, MED SCI MONITOR, V16, pCR357