Targeting SET/I2PP2A oncoprotein functions as a multi-pathway strategy for cancer therapy-Reference-Cited by-同舟云学术

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Targeting SET/I2PP2A oncoprotein functions as a multi-pathway strategy for cancer therapy

Published:2011-02-07 Issue:22 Volume:30 Page:2504-2513
ISSN:0950-9232
Container-title:Oncogene
language:en
Short-container-title:Oncogene

Author:

Switzer C H,Cheng R Y S,Vitek T M,Christensen D J,Wink D A,Vitek M P

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Link

http://www.nature.com/articles/onc2010622.pdf

Reference49 articles.

1. Adachi Y, Pavlakis GN, Copeland TD . (1994). Identification and characterization of SET, a nuclear phosphoprotein encoded by the translocation break point in acute undifferentiated leukemia. J Biol Chem 269: 2258–2262.

2. Arnold H, Sears R . (2008). A tumor suppressor role for PP2A-B56α through negative regulation of c-Myc and other key oncoproteins. Cancer Metastasis Rev 27: 147–158.

3. Arnold HK, Sears RC . (2006). Protein phosphatase 2A regulatory subunit B56(alpha) associates with c-Myc and negatively regulates c-Myc accumulation. Mol Cell Biol 26: 2832–2844.

4. Canela N, Rodriguez-Vilarrupla A, Estanyol JM, Diaz C, Pujol MJ, Agell N et al. (2003). The SET protein regulates G2/M transition by modulating cyclin B-cyclin-dependent kinase 1 activity. J Biol Chem 278: 1158–1164.

5. Carlson SG, Eng E, Kim EG, Perlman EJ, Copeland TD, Ballermann BJ . (1998). Expression of SET, an inhibitor of protein phosphatase 2A, in renal development and Wilms’ tumor. J Am Soc Nephrol 9: 1873–1880.

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