Targeting cancer with small molecule kinase inhibitors

被引:2071
作者
Zhang, Jianming [1 ]
Yang, Priscilla L. [2 ]
Gray, Nathanael S. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Dana Farber Canc Inst,Dept Canc Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
CHRONIC MYELOID-LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; RECEPTOR TYROSINE KINASE; ACTIVATED PROTEIN-KINASE; GROWTH-FACTOR RECEPTOR; RIBOSOMAL S6 KINASE; ABL KINASE; BCR-ABL; ANTITUMOR-ACTIVITY; CRYSTAL-STRUCTURE;
D O I
10.1038/nrc2559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Deregulation of kinase activity has emerged as a major mechanism by which cancer cells evade normal physiological constraints on growth and survival. To date, 11 kinase inhibitors have received US Food and Drug Administration approval as cancer treatments, and there are considerable efforts to develop selective small molecule inhibitors for a host of other kinases that are implicated in cancer and other diseases. Herein we discuss the current challenges in the field, such as designing selective inhibitors and developing strategies to overcome resistance mutations. This Review provides a broad overview of some of the approaches currently used to discover and characterize new kinase inhibitors.
引用
收藏
页码:28 / 39
页数:12
相关论文
共 105 条
  • [1] Allosteric inhibitors of Bcr-abl-dependent cell proliferation
    Adrián, FJ
    Ding, Q
    Sim, TB
    Velentza, A
    Sloan, C
    Liu, Y
    Zhang, GB
    Hur, W
    Ding, S
    Manley, P
    Mestan, J
    Fabbro, D
    Gray, NS
    [J]. NATURE CHEMICAL BIOLOGY, 2006, 2 (02) : 95 - 102
  • [2] The PIK3CA gene is mutated with high frequency in human breast cancers
    Bachman, KE
    Argani, P
    Samuels, Y
    Silliman, N
    Ptak, J
    Szabo, S
    Konishi, H
    Karakas, B
    Blair, BG
    Lin, C
    Peters, BA
    Velculescu, VE
    Park, BH
    [J]. CANCER BIOLOGY & THERAPY, 2004, 3 (08) : 772 - 775
  • [3] The selectivity of protein kinase inhibitors: a further update
    Bain, Jenny
    Plater, Lorna
    Elliott, Matt
    Shpiro, Natalia
    Hastie, C. James
    Mclauchlan, Hilary
    Klevernic, Iva
    Arthur, J. Simon C.
    Alessi, Dario R.
    Cohen, Philip
    [J]. BIOCHEMICAL JOURNAL, 2007, 408 : 297 - 315
  • [4] Quantitative chemical proteomics reveals mechanisms of action of clinical ABL kinase inhibitors
    Bantscheff, Marcus
    Eberhard, Dirk
    Abraham, Yann
    Bastuck, Sonja
    Boesche, Markus
    Hobson, Scott
    Mathieson, Toby
    Perrin, Jessica
    Raida, Manfred
    Rau, Christina
    Reader, Valerie
    Sweetman, Gavain
    Bauer, Andreas
    Bouwmeester, Tewis
    Hopf, Carsten
    Kruse, Ulrich
    Neubauer, Gitte
    Ramsden, Nigel
    Rick, Jens
    Kuster, Bernhard
    Drewes, Gerard
    [J]. NATURE BIOTECHNOLOGY, 2007, 25 (09) : 1035 - 1044
  • [5] Identification and characterization of pleckstrin-homology-domain-dependent and isoenzyme-specific Akt inhibitors
    Barnett, SF
    Defeo-Jones, D
    Fu, S
    Hancock, PJ
    Haskell, KM
    Jones, RE
    Kahana, JA
    Kral, AM
    Leander, K
    Lee, LL
    Malinowski, J
    McAvoy, EM
    Nahas, DD
    Robinson, RG
    Huber, HE
    [J]. BIOCHEMICAL JOURNAL, 2005, 385 : 399 - 408
  • [6] Characterization of a conserved structural determinant controlling protein kinase sensitivity to selective inhibitors
    Blencke, S
    Zech, B
    Engkvist, O
    Greff, Z
    Örfi, L
    Horváth, Z
    Kéri, G
    Ullrich, A
    Daub, H
    [J]. CHEMISTRY & BIOLOGY, 2004, 11 (05): : 691 - 701
  • [7] PHA-739358, a potent inhibitor of Aurora kinases with a selective target inhibition profile relevant to cancer
    Carpinelli, Patrizia
    Ceruti, Roberta
    Giorgini, Maria Laura
    Cappella, Paolo
    Gianellini, Laura
    Croci, Valter
    Degrassi, Anna
    Texido, Gernma
    Rocchetti, Maurizio
    Vianello, Paola
    Rusconi, Luisa
    Storici, Paola
    Zugnoni, Paola
    Arrigoni, Claudio
    Soncini, Chiara
    Alli, Cristina
    Patton, Veronica
    Marsiglio, Aurelio
    Ballinari, Dario
    Pesenti, Enrico
    Fancelli, Daniele
    Moll, Jurgen
    [J]. MOLECULAR CANCER THERAPEUTICS, 2007, 6 (12) : 3158 - 3168
  • [8] Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases
    Carter, TA
    Wodicka, LM
    Shah, NP
    Velasco, AM
    Fabian, MA
    Treiber, DK
    Milanov, ZV
    Atteridge, CE
    Biggs, WH
    Edeen, PT
    Floyd, M
    Ford, JM
    Grotzfeld, RM
    Herrgard, S
    Insko, DE
    Mehta, SA
    Patel, HK
    Pao, W
    Sawyers, CL
    Varmus, H
    Zarrinkar, PP
    Lockhart, DJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (31) : 11011 - 11016
  • [9] The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
    Christofk, Heather R.
    Vander Heiden, Matthew G.
    Harris, Marian H.
    Ramanathan, Arvind
    Gerszten, Robert E.
    Wei, Ru
    Fleming, Mark D.
    Schreiber, Stuart L.
    Cantley, Lewis C.
    [J]. NATURE, 2008, 452 (7184) : 230 - U74
  • [10] Detection of BCR-ABL kinase mutations in CD34+ cells from chronic myelogenous leukemia patients in complete cytogenetic remission on imatinib mesylate treatment
    Chu, S
    Xu, H
    Shah, NP
    Snyder, DS
    Forman, SJ
    Sawyers, CL
    Bhatia, R
    [J]. BLOOD, 2005, 105 (05) : 2093 - 2098