Harnessing synthetic lethal interactions in anticancer drug discovery

被引:201
作者
Chan, Denise A. [2 ]
Giaccia, Amato J. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Radiat Oncol, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA 94143 USA
关键词
GROWTH-FACTOR RECEPTOR; RENAL-CELL CARCINOMA; CANCER SUSCEPTIBILITY GENE; ABL TYROSINE KINASE; DNA POLYMERASE-BETA; POLY(ADP-RIBOSE) POLYMERASE; HOMOLOGOUS RECOMBINATION; SELECTIVE INHIBITOR; MOLECULAR TARGETS; INTERFERON-ALPHA;
D O I
10.1038/nrd3374
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Unique features of tumours that can be exploited by targeted therapies are a key focus of current cancer research. One such approach is known as synthetic lethality screening, which involves searching for genetic interactions of two mutations whereby the presence of either mutation alone has no effect on cell viability but the combination of the two mutations results in cell death. The presence of one of these mutations in cancer cells but not in normal cells can therefore create opportunities to selectively kill cancer cells by mimicking the effect of the second genetic mutation with targeted therapy. Here, we summarize strategies that can be used to identify synthetic lethal interactions for anticancer drug discovery, describe examples of such interactions that are currently being investigated in preclinical and clinical studies of targeted anticancer therapies, and discuss the challenges of realizing the full potential of such therapies.
引用
收藏
页码:351 / 364
页数:14
相关论文
共 138 条
[1]   Kinase inhibition with BAY 43-9006 n renal cell carcinoma [J].
Ahmad, T ;
Eisen, T .
CLINICAL CANCER RESEARCH, 2004, 10 (18) :6388S-6392S
[2]   Role of Tyrosine Kinase Inhibitors in Lung Cancer [J].
Ansari, J. ;
Palmer, D. H. ;
Rea, D. W. ;
Hussain, S. A. .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2009, 9 (05) :569-575
[3]   A synthetic lethal therapeutic approach: Poly(ADP) ribose polymerase inhibitors for the treatment of cancers deficient in DNA double-strand break repair [J].
Ashworth, Alan .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (22) :3785-3790
[4]   Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial [J].
Audeh, M. William ;
Carmichael, James ;
Penson, Richard T. ;
Friedlander, Michael ;
Powell, Bethan ;
Bell-McGuinn, Katherine M. ;
Scott, Clare ;
Weitzel, Jeffrey N. ;
Oaknin, Ana ;
Loman, Niklas ;
Lu, Karen ;
Schmutzler, Rita K. ;
Matulonis, Ursula ;
Wickens, Mark ;
Tutt, Andrew .
LANCET, 2010, 376 (9737) :245-251
[5]   INHIBITORS AND ACTIVATORS OF ADP-RIBOSYLATION REACTIONS [J].
BANASIK, M ;
UEDA, K .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1994, 138 (1-2) :185-197
[6]   Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1 [J].
Barbie, David A. ;
Tamayo, Pablo ;
Boehm, Jesse S. ;
Kim, So Young ;
Moody, Susan E. ;
Dunn, Ian F. ;
Schinzel, Anna C. ;
Sandy, Peter ;
Meylan, Etienne ;
Scholl, Claudia ;
Froehling, Stefan ;
Chan, Edmond M. ;
Sos, Martin L. ;
Michel, Kathrin ;
Mermel, Craig ;
Silver, Serena J. ;
Weir, Barbara A. ;
Reiling, Jan H. ;
Sheng, Qing ;
Gupta, Piyush B. ;
Wadlow, Raymond C. ;
Le, Hanh ;
Hoersch, Sebastian ;
Wittner, Ben S. ;
Ramaswamy, Sridhar ;
Livingston, David M. ;
Sabatini, David M. ;
Meyerson, Matthew ;
Thomas, Roman K. ;
Lander, Eric S. ;
Mesirov, Jill P. ;
Root, David E. ;
Gilliland, D. Gary ;
Jacks, Tyler ;
Hahn, William C. .
NATURE, 2009, 462 (7269) :108-U122
[7]   USE OF A SCREEN FOR SYNTHETIC LETHAL AND MULTICOPY SUPPRESSEE MUTANTS TO IDENTIFY 2 NEW GENES INVOLVED IN MORPHOGENESIS IN SACCHAROMYCES-CEREVISIAE [J].
BENDER, A ;
PRINGLE, JR .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1295-1305
[8]   The breast cancer susceptibility gene BRCA1 is required for subnuclear assembly of Rad51 and survival following treatment with the DNA cross-linking agent cisplatin [J].
Bhattacharyya, A ;
Ear, US ;
Koller, BH ;
Weichselbaum, RR ;
Bishop, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23899-23903
[9]   Down-regulation of Rad51 and decreased homologous recombination in hypoxic cancer cells [J].
Bindra, RS ;
Schaffer, PJ ;
Meng, A ;
Woo, J ;
Måseide, K ;
Roth, ME ;
Lizardi, P ;
Hedley, DW ;
Bristow, RG ;
Glazer, PM .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (19) :8504-8518
[10]   Kinase requirements in human cells: III. Altered kinase requirements in VHL-/- cancer cells detected in a pilot synthetic lethal screen [J].
Bommi-Reddy, Archana ;
Almeciga, Ingrid ;
Sawyer, Jacqueline ;
Geisen, Christoph ;
Li, Wenliang ;
Harlow, Ed ;
Kaelin, William G., Jr. ;
Grueneberg, Dorre A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (43) :16484-16489