Key drivers of biomedical innovation in cancer drug discovery

被引:4
作者
Huber, Margit A. [1 ]
Kraut, Norbert [2 ]
机构
[1] Univ Ulm, Dept Dermatol & Allerg Dis, D-89069 Ulm, Germany
[2] Boehringer Ingelheim RCV GmbH & Co KG, Oncol Res, Vienna, Austria
关键词
CELL LUNG-CANCER; SELECTIVE INHIBITOR; MUTATIONS; KINASE; POTENT; BRAF; MELANOMA; LESSONS; TUMORS; GENE;
D O I
10.15252/emmm.201404596
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Discovery and translational research has led to the identification of a series of "cancer drivers"-genes that, when mutated or otherwise misregulated, can drive malignancy. An increasing number of drugs that directly target such drivers have demonstrated activity in clinical trials and are shaping a new landscape for molecularly targeted cancer therapies. Such therapies rely on molecular and genetic diagnostic tests to detect the presence of a biomarker that predicts response. Here, we highlight some of the key discoveries bringing precision oncology to cancer patients. Large-scale "omics" approaches as well as modern, hypothesis-driven science in both academic and industry settings have significantly contributed to the field. Based on these insights, we discuss current challenges and how to foster future biomedical innovation in cancer drug discovery and development.
引用
收藏
页码:12 / 16
页数:5
相关论文
共 40 条
[1]  
[Anonymous], J CLIN ONCOL S
[2]  
[Anonymous], J CLIN ONCOL S
[3]  
[Anonymous], P 105 ANN M AM ASS C
[4]  
[Anonymous], J CLIN ONCOL S
[6]   Vemurafenib: the first drug approved for BRAF-mutant cancer [J].
Bollag, Gideon ;
Tsai, James ;
Zhang, Jiazhong ;
Zhang, Chao ;
Ibrahim, Prabha ;
Nolop, Keith ;
Hirth, Peter .
NATURE REVIEWS DRUG DISCOVERY, 2012, 11 (11) :873-886
[7]   Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase [J].
Bryant, HE ;
Schultz, N ;
Thomas, HD ;
Parker, KM ;
Flower, D ;
Lopez, E ;
Kyle, S ;
Meuth, M ;
Curtin, NJ ;
Helleday, T .
NATURE, 2005, 434 (7035) :913-917
[8]   Activity and safety of crizotinib in patients with ALK-positive non-small-cell lung cancer: updated results from a phase 1 study [J].
Camidge, D. Ross ;
Bang, Yung-Jue ;
Kwak, Eunice L. ;
Iafrate, A. John ;
Varella-Garcia, Marileila ;
Fox, Stephen B. ;
Riely, Gregory J. ;
Solomon, Benjamin ;
Ou, Sai-Hong I. ;
Kim, Dong-Wan ;
Salgia, Ravi ;
Fidias, Panagiotis ;
Engelman, Jeffrey A. ;
Gandhi, Leena ;
Jaenne, Pasi A. ;
Costa, Daniel B. ;
Shapiro, Geoffrey I. ;
LoRusso, Patricia ;
Ruffner, Katherine ;
Stephenson, Patricia ;
Tang, Yiyun ;
Wilner, Keith ;
Clark, Jeffrey W. ;
Shaw, Alice T. .
LANCET ONCOLOGY, 2012, 13 (10) :1011-1019
[9]   Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer [J].
Cheung, Hiu Wing ;
Cowley, Glenn S. ;
Weir, Barbara A. ;
Boehm, Jesse S. ;
Rusin, Scott ;
Scott, Justine A. ;
East, Alexandra ;
Ali, Levi D. ;
Lizotte, Patrick H. ;
Wong, Terence C. ;
Jiang, Guozhi ;
Hsiao, Jessica ;
Mermel, Craig H. ;
Getz, Gad ;
Barretina, Jordi ;
Gopal, Shuba ;
Tamayo, Pablo ;
Gould, Joshua ;
Tsherniak, Aviad ;
Stransky, Nicolas ;
Luo, Biao ;
Ren, Yin ;
Drapkin, Ronny ;
Bhatia, Sangeeta N. ;
Mesirov, Jill P. ;
Garraway, Levi A. ;
Meyerson, Matthew ;
Lander, Eric S. ;
Root, David E. ;
Hahn, William C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (30) :12372-12377
[10]   Potent inhibition of DOT1L as treatment of MLL-fusion leukemia [J].
Daigle, Scott R. ;
Olhava, Edward J. ;
Therkelsen, Carly A. ;
Basavapathruni, Aravind ;
Jin, Lei ;
Boriack-Sjodin, P. Ann ;
Allain, Christina J. ;
Klaus, Christine R. ;
Raimondi, Alejandra ;
Scott, Margaret Porter ;
Waters, Nigel J. ;
Chesworth, Richard ;
Moyer, Mikel P. ;
Copeland, Robert A. ;
Richon, Victoria M. ;
Pollock, Roy M. .
BLOOD, 2013, 122 (06) :1017-1025