Targeting inhibitor 2 of protein phosphatase 2A as a therapeutic strategy for prostate cancer treatment

被引:24
作者
Mukhopadhyay, Archana [1 ]
Tabanor, Kayann [1 ]
Chaguturu, Rathnam [1 ,2 ]
Aldrich, Jane V. [3 ]
机构
[1] Univ Kansas, Higuchi Biosci Ctr, Lawrence, KS 66045 USA
[2] SRI Int, Ctr Adv Drug Res, Harrisonburg, VA USA
[3] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
关键词
inhibitor 2 of protein phosphatase 2A; ceramide; tumor suppressor lipid; protein phosphatase 2A; c-Myc; cell signaling; histone acetyl transferase; TUMOR-SUPPRESSOR PP2A; HISTONE ACETYLATION; PHOSPHOPROTEIN SET; IN-VITRO; C-MYC; CERAMIDE; EXPRESSION; SPHINGOLIPIDS; HYPERACETYLATION; IDENTIFICATION;
D O I
10.4161/cbt.25943
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Inhibitor 2 of protein phosphatase 2A (I2PP2A), a biological inhibitor of the cellular serine/threonine protein phosphatase PP2A, is associated with numerous cellular processes that often lead to the formation and progression of cancer. In this study we hypothesized that targeting the inhibition of I2PP2A's multiple functions in prostate cancer cells might prevent cancer progression. We have investigated the effect of the small chain C6-ceramide, known to be a bioactive tumor suppressor lipid, on I2PP2A function, thereby affecting c-Myc signaling and histone acetylation in cells. Our data indicated that C6-ceramide treatment of prostate cancer cells induces cell death in PC-3, DU145, and LNCaP cells, but not normal prostate epithelial cells. C6-ceramide was able to disrupt the association between PP2A and I2PP2A. C6-ceramide inhibits I2PP2A's upregulation of c-Myc and downregulation of histone acetylation in prostate cancer cells. Our data indicated that targeting cancer related signaling pathways through I2PP2A using ceramide as an anti-I2PP2A agent could have beneficial effects as a therapeutic approach to prevent prostate cancer.
引用
收藏
页码:962 / 972
页数:11
相关论文
共 53 条
  • [1] ADACHI Y, 1994, J BIOL CHEM, V269, P2258
  • [2] PCOTH, a novel gene overexpressed in prostate cancers, promotes prostate cancer cell growth through phosphorylation of oncoprotein TAF-lβ/SET
    Anazawa, Y
    Nakagawa, H
    Furihara, M
    Ashida, S
    Tamura, K
    Yoshioka, H
    Shuin, T
    Fujioka, T
    Katagiri, T
    Nakamura, Y
    [J]. CANCER RESEARCH, 2005, 65 (11) : 4578 - 4586
  • [3] Protein phosphatase 2A regulatory subunit b56α associates with c-Myc and negatively regulates c-Myc accumulation
    Arnold, HK
    Sears, RC
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (07) : 2832 - 2844
  • [4] A tumor suppressor role for PP2A-B56α through negative regulation of c-Myc and other key oncoproteins
    Arnold, Hugh K.
    Sears, Rosalie C.
    [J]. CANCER AND METASTASIS REVIEWS, 2008, 27 (02) : 147 - 158
  • [5] Simultaneous quantitative analysis of bioactive sphingolipids by high-performance liquid chromatography-tandem mass spectrometry
    Bielawski, Jacek
    Szulc, Zdzislaw M.
    Hannun, Yusuf A.
    Bielawska, Alicja
    [J]. METHODS, 2006, 39 (02) : 82 - 91
  • [6] The SET protein regulates G2/M transition by modulating cyclin B-cyclin-dependent kinase 1 activity
    Canela, N
    Rodriguez-Vilarrupla, A
    Estanyol, JM
    Díaz, C
    Pujol, MJ
    Agell, N
    Bachs, O
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) : 1158 - 1164
  • [7] Carlson SG, 1998, J AM SOC NEPHROL, V9, P1873
  • [8] Glyceraldehyde 3-phosphate dehydrogenase is a SET-binding protein and regulates cyclin B-cdk1 activity
    Carujo, S.
    Estanyol, J. M.
    Ejarque, A.
    Agell, N.
    Bachs, O.
    Pujol, M. J.
    [J]. ONCOGENE, 2006, 25 (29) : 4033 - 4042
  • [9] Novel role for the nuclear phosphoprotein SET in transcriptional activation of P450c17 and initiation of neurosteroidogenesis
    Compagnone, NA
    Zhang, P
    Vigne, JL
    Mellon, SH
    [J]. MOLECULAR ENDOCRINOLOGY, 2000, 14 (06) : 875 - 888
  • [10] Reducing prohibitin increases histone acetylation, and promotes androgen independence in prostate tumours by increasing androgen receptor activation by adrenal androgens
    Dart, D. A.
    Brooke, G. N.
    Sita-Lumsden, A.
    Waxman, J.
    Bevan, C. L.
    [J]. ONCOGENE, 2012, 31 (43) : 4588 - 4598