Optimization of novel nipecotic bis(amide) inhibitors of the Rho/MKL1/SRF transcriptional pathway as potential anti-metastasis agents

被引:62
作者
Bell, Jessica L.
Haak, Andrew J. [1 ]
Wade, Susan M. [1 ]
Kirchhoff, Paul D.
Neubig, Richard R. [1 ,2 ,3 ]
Larsen, Scott D. [3 ]
机构
[1] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Ctr Chem Genom, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Ctr Discovery New Med, Ann Arbor, MI 48109 USA
关键词
Anti-metastasis; Rho; MKL1; SRF; Cancer; Gene transcription inhibitor; Cell migration inhibition; RHOC GTPASE; CANCER; IDENTIFICATION; TARGETS; KINASE; SRF;
D O I
10.1016/j.bmcl.2013.04.080
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
CCG-1423 (1) is a novel inhibitor of Rho/MKL1/SRF-mediated gene transcription that inhibits invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis. We recently reported the design and synthesis of conformationally restricted analogs (e.g., 2) with improved selectivity for inhibiting invasion versus acute cytotoxicity. In this study we conducted a survey of aromatic substitution with the goal of improving physicochemical parameters (e.g., Clog P, MW) for future efficacy studies in vivo. Two new compounds were identified that attenuated cytotoxicity even further, and were fourfold more potent than 2 at inhibiting PC-3 cell migration in a scratch wound assay. One of these (8a, CCG-203971, IC50 = 4.2 mu M) was well tolerated in mice for 5 days at 100 mg/kg/day i.p., and was able to achieve plasma levels exceeding the migration IC50 for up to 3 h. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3826 / 3832
页数:7
相关论文
共 20 条
  • [1] Megakaryoblastic leukemia 1, a potent transcriptional coactivator for serum response factor (SRF), is required for serum induction of SRF target genes
    Cen, B
    Selvaraj, A
    Burgess, RC
    Hitzler, JK
    Ma, ZG
    Morris, SW
    Prywes, R
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (18) : 6597 - 6608
  • [2] Genomic analysis of metastasis reveals an essential role for RhoC
    Clark, EA
    Golub, TR
    Lander, ES
    Hynes, RO
    [J]. NATURE, 2000, 406 (6795) : 532 - 535
  • [3] CCG-1423:: a small-molecule inhibitor of RhoA transcriptional signaling
    Evelyn, Chris R.
    Wade, Susan M.
    Wang, Qin
    Wu, Mei
    Iniguez-Lluhi, Jorge A.
    Merajver, Sofia D.
    Neubig, Richard R.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2007, 6 (08) : 2249 - 2260
  • [4] Design, synthesis and prostate cancer cell-based studies of analogs of the Rho/MKL1 transcriptional pathway inhibitor, CCG-1423
    Evelyn, Chris R.
    Bell, Jessica L.
    Ryu, Jenny G.
    Wade, Susan M.
    Kocab, Andrew
    Harzdorf, Nicole L.
    Showalter, H. D. Hollis
    Neubig, Richard R.
    Larsen, Scott D.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (02) : 665 - 672
  • [5] RhoC is dispensable for embryogenesis and tumor initiation but essential for metastasis
    Hakem, A
    Sanchez-Sweatman, O
    You-Ten, A
    Duncan, G
    Wakeham, A
    Khokha, R
    Mak, TW
    [J]. GENES & DEVELOPMENT, 2005, 19 (17) : 1974 - 1979
  • [6] MScreen: An Integrated Compound Management and High-Throughput Screening Data Storage and Analysis System
    Jacob, Renju T.
    Larsen, Martha J.
    Larsen, Scott D.
    Kirchhoff, Paul D.
    Sherman, David H.
    Neubig, Richard R.
    [J]. JOURNAL OF BIOMOLECULAR SCREENING, 2012, 17 (08) : 1080 - 1087
  • [7] The Rho/ROCK pathway for lysophosphatidic acid-induced proteolytic enzyme expression and ovarian cancer cell invasion
    Jeong, K. J.
    Park, S. Y.
    Cho, K. H.
    Sohn, J. S.
    Lee, J.
    Kim, Y. K.
    Kang, J.
    Park, C. G.
    Han, J. W.
    Lee, H. Y.
    [J]. ONCOGENE, 2012, 31 (39) : 4279 - 4289
  • [8] Kerns EH, 2008, DRUG-LIKE PROPERTIES: CONCEPTS, STRUCTURE DESIGN AND METHODS, P299, DOI 10.1016/B978-012369520-8.50028-0
  • [9] Lawrence R. M., 1997, SYNTHESIS-STUTTGART, V1997, P553
  • [10] Identification of the cellular targets of bioactive small organic molecules using affinity reagents
    Leslie, Benjamin J.
    Hergenrother, Paul J.
    [J]. CHEMICAL SOCIETY REVIEWS, 2008, 37 (07) : 1347 - 1360