Expression of αCP-4 inhibits cell cycle progression and suppresses tumorigenicity of lung cancer cells

被引:20
作者
Castano, Zatira [1 ]
Vergara-Irigaray, Nuria [1 ]
Pajares, Maria J. [1 ,2 ,3 ]
Montuenga, Luis M. [1 ,2 ,3 ]
Pio, Ruben [1 ,3 ,4 ]
机构
[1] Univ Navarra, Div Oncol, CIMA, Pamplona 31008, Spain
[2] Univ Navarra, Sch Med, Dept Histol & Pathol, E-31080 Pamplona, Spain
[3] Univ Navarra, Sch Sci, E-31080 Pamplona, Spain
[4] Univ Navarra, Sch Med, Dept Biochem, E-31080 Pamplona, Spain
关键词
alpha CP-4; PCBP4; hnRNP E4; RNA binding protein; tumor suppressor gene; lung cancer;
D O I
10.1002/ijc.23236
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The protein alpha CP-4 (also known as hnRNP E4) is an RNA binding protein encoded by a gene at 3p21, one of the most common altered regions in lung cancer. It has been proposed that aCP-4 may function as a lung tumor suppressor. Lack of aCP-4 expression is frequent in highly proliferative lung tumors and correlates with alpha CP-4 allele losses. The aim of this study was to evaluate the effect of aCP-4 on the tumorigenic capacity of lung cancer cells. aCP-4 expression was induced by transient transfection or stable infection with recombinant retroviruses. Induction of aCP-4 expression caused cell cycle arrest in G(2)/M in 3 out of the 7 lung cancer cell lines studied, while no effect on apoptosis was observed. Anchorage-independent growth and invasion capacity of H1299 cells were significantly reduced by alpha CP-4 induction. Tumorigenicity of H1299 cells in nude mice was greatly inhibited by the expression of aCP-4. Moreover, induction of aCP-4 expression in already established tumors resulted in a sudden growth arrest. Immunocytochemistry analysis of the xenograft tumors revealed an in vivo effect of aCP-4 on cell proliferation and no effect on apoptosis. Finally, alpha CP-4 showed a subcellular localization different from alpha CP-4a, a splice variant that does not affect cell proliferation. In conclusion, expression of alpha CP-4 can inhibit proliferation and tumorigenesis of lung cancer cells, both in vivo and in vitro, by delaying the progression of the cell cycle. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1512 / 1520
页数:9
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