Loss of p14ARF in tumor cells facilitates replication of the adenovirus mutant dl1520 (ONYX-015)

被引:165
|
作者
Ries, SJ
Brandts, CH
Chung, AS
Biederer, CH
Hann, BC
Lipner, EM
McCormick, F
Korn, WM [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, Div Gastroenterol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, Canc Res Inst, San Francisco, CA 94143 USA
关键词
D O I
10.1038/80466
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The adenovirus mutant dl1520 (ONYX-015) does not express the E1B-55K protein that binds and inactivates p53. This virus replicates in tumor cells with mutant p53, but not in normal cells with functional p53. Although intra-tumoral injection of dl1520 shows promising responses in patients with solid tumors, previous in vitro studies have not established a close correlation between p53 status and dl1520 replication. Here we identify loss of p14(ARF) as a mechanism that allows dl1520 replication in tumor cells retaining wild-type p53. We demonstrate that the re-introduction of p14(ARF) into tumor cells with wild-type p53 suppresses replication of dl1520 in a p53-dependent manner. Our study supports the therapeutic use of dl1520 in tumors with lesions within the p53 pathway other than mutation of p53.
引用
收藏
页码:1128 / 1133
页数:6
相关论文
共 46 条
  • [41] Adenovirus-mediated p14ARF gene transfer cooperates with Ad5CMV-p53 to induce apoptosis in human cancer cells
    Tango, Y
    Fujiwara, T
    Itoshima, T
    Takata, Y
    Katsuda, K
    Uno, F
    Ohtani, S
    Tani, T
    Roth, JA
    Tanaka, N
    [J]. HUMAN GENE THERAPY, 2002, 13 (11) : 1373 - 1382
  • [42] Apoptosis induced by adenovirus-mediated p14ARF expression in U2OS osteosarcoma cells is associated with increased Fas expression
    Kim, M
    Sgagias, M
    Deng, XY
    Jung, YJ
    Rikiyama, T
    Lee, K
    Ouellette, M
    Cowan, K
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (01) : 138 - 144
  • [44] A comparison analysis of anti-tumor efficacy of adenoviral gene replacement therapy (p14ARF and p16INK4A) in human mesothelioma cells
    Yang, CT
    You, L
    Lin, YC
    Lin, CL
    McCormick, F
    Jablons, DM
    [J]. ANTICANCER RESEARCH, 2003, 23 (1A) : 33 - 38
  • [45] The p14ARF tumor suppressor protein facilitates nucleolar sequestration of hypoxia-inducible factor-1α (HIF-1α) and inhibits HIF-1-mediated transcription
    Fatyol, K
    Szalay, AA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (30) : 28421 - 28429
  • [46] E1B55K-deleted adenovirus (ONYX-015) overrides G1/S and G2/M checkpoints and causes mitotic catastrophe and endoreduplication in p53-proficient normal cells
    Cherubini, Gioia
    Petouchoff, Tatiana
    Grossi, Milena
    Piersanti, Stefania
    Cundari, Enrico
    Saggio, Isabella
    [J]. CELL CYCLE, 2006, 5 (19) : 2244 - 2252