Gene isoforms as expression-based biomarkers predictive of drug response in vitro

被引:50
作者
Safikhani, Zhaleh [1 ,2 ]
Smirnov, Petr [1 ]
Thu, Kelsie L. [1 ,3 ]
Silvester, Jennifer [1 ,3 ]
El-Hachem, Nehme [3 ]
Quevedo, Rene [1 ,2 ]
Lupien, Mathieu [1 ,2 ]
Mak, Tak W. [1 ,2 ,4 ]
Cescon, David [1 ,4 ,5 ]
Haibe-Kains, Benjamin [1 ,2 ,6 ,7 ]
机构
[1] Univ Hlth Network, Princess Margaret Canc Ctr, 101 Coll St, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Dept Med Biophys, 101 Coll St, Toronto, ON M5G 1L7, Canada
[3] Inst Rech Clin Montreal, 110 Pine Ave West, Montreal, PQ H2W 1R7, Canada
[4] Campbell Family Inst Breast Canc Res, 620 Univ Ave, Toronto, ON M5G 2C1, Canada
[5] Univ Toronto, Div Med Oncol & Hematol, Dept Med, 27 Kings Coll Circle, Toronto, ON M5S 1A1, Canada
[6] Univ Toronto, Dept Comp Sci, 10 Kings Coll Rd, Toronto, ON M5S 3G4, Canada
[7] Ontario Inst Canc Res, 661 Univ Ave,Suite 510, Toronto, ON M5G 0A3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
RNA-SEQ EXPERIMENTS; CELL-LINES; CANCER; SENSITIVITY; IDENTIFICATION; RESISTANCE; REPRODUCIBILITY; QUANTIFICATION; TRANSCRIPTOME; ALGORITHMS;
D O I
10.1038/s41467-017-01153-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Next-generation sequencing technologies have recently been used in pharmacogenomic studies to characterize large panels of cancer cell lines at the genomic and transcriptomic levels. Among these technologies, RNA-sequencing enable profiling of alternatively spliced transcripts. Given the high frequency of mRNA splicing in cancers, linking this feature to drug response will open new avenues of research in biomarker discovery. To identify robust transcriptomic biomarkers for drug response across studies, we develop a meta-analytical framework combining the pharmacological data from two large-scale drug screening datasets. We use an independent pan-cancer pharmacogenomic dataset to test the robustness of our candidate biomarkers across multiple cancer types. We further analyze two independent breast cancer datasets and find that specific isoforms of IGF2BP2, NECTIN4, ITGB6, and KLHDC9 are significantly associated with AZD6244, lapatinib, erlotinib, and paclitaxel, respectively. Our results support isoform expressions as a rich resource for biomarkers predictive of drug response.
引用
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页数:11
相关论文
共 63 条
[1]   Direct integrin αvβ6-ERK binding:: implications for tumour growth [J].
Ahmed, N ;
Niu, J ;
Dorahy, DJ ;
Gu, XH ;
Andrews, S ;
Meldrum, CJ ;
Scott, RJ ;
Baker, MS ;
Macreadie, IG ;
Agrez, MV .
ONCOGENE, 2002, 21 (09) :1370-1380
[2]   The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity [J].
Barretina, Jordi ;
Caponigro, Giordano ;
Stransky, Nicolas ;
Venkatesan, Kavitha ;
Margolin, Adam A. ;
Kim, Sungjoon ;
Wilson, Christopher J. ;
Lehar, Joseph ;
Kryukov, Gregory V. ;
Sonkin, Dmitriy ;
Reddy, Anupama ;
Liu, Manway ;
Murray, Lauren ;
Berger, Michael F. ;
Monahan, John E. ;
Morais, Paula ;
Meltzer, Jodi ;
Korejwa, Adam ;
Jane-Valbuena, Judit ;
Mapa, Felipa A. ;
Thibault, Joseph ;
Bric-Furlong, Eva ;
Raman, Pichai ;
Shipway, Aaron ;
Engels, Ingo H. ;
Cheng, Jill ;
Yu, Guoying K. ;
Yu, Jianjun ;
Aspesi, Peter, Jr. ;
de Silva, Melanie ;
Jagtap, Kalpana ;
Jones, Michael D. ;
Wang, Li ;
Hatton, Charles ;
Palescandolo, Emanuele ;
Gupta, Supriya ;
Mahan, Scott ;
Sougnez, Carrie ;
Onofrio, Robert C. ;
Liefeld, Ted ;
MacConaill, Laura ;
Winckler, Wendy ;
Reich, Michael ;
Li, Nanxin ;
Mesirov, Jill P. ;
Gabriel, Stacey B. ;
Getz, Gad ;
Ardlie, Kristin ;
Chan, Vivien ;
Myer, Vic E. .
NATURE, 2012, 483 (7391) :603-607
[3]   mRNA Transcript Diversity Creates New Opportunities for Pharmacological Intervention [J].
Barrie, Elizabeth S. ;
Smith, Ryan M. ;
Sanford, Jonathan C. ;
Sadee, Wolfgang .
MOLECULAR PHARMACOLOGY, 2012, 81 (05) :620-630
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   Efficient RNA isoform identification and quantification from RNA-Seq data with network flows [J].
Bernard, Elsa ;
Jacob, Laurent ;
Mairal, Julien ;
Vert, Jean-Philippe .
BIOINFORMATICS, 2014, 30 (17) :2447-2455
[6]   An overview of ensembl [J].
Birney, E ;
Andrews, TD ;
Bevan, P ;
Caccamo, M ;
Chen, Y ;
Clarke, L ;
Coates, G ;
Cuff, J ;
Curwen, V ;
Cutts, T ;
Down, T ;
Eyras, E ;
Fernandez-Suarez, XM ;
Gane, P ;
Gibbins, B ;
Gilbert, J ;
Hammond, M ;
Hotz, HR ;
Iyer, V ;
Jekosch, K ;
Kahari, A ;
Kasprzyk, A ;
Keefe, D ;
Keenan, S ;
Lehvaslaiho, H ;
McVicker, G ;
Melsopp, C ;
Meidl, P ;
Mongin, E ;
Pettett, R ;
Potter, S ;
Proctor, G ;
Rae, M ;
Searle, S ;
Slater, G ;
Smedley, D ;
Smith, J ;
Spooner, W ;
Stabenau, A ;
Stalker, J ;
Storey, R ;
Ureta-Vidal, A ;
Woodwark, KC ;
Cameron, G ;
Durbin, R ;
Cox, A ;
Hubbard, T ;
Clamp, M .
GENOME RESEARCH, 2004, 14 (05) :925-928
[7]   Near-optimal probabilistic RNA-seq quantification [J].
Bray, Nicolas L. ;
Pimentel, Harold ;
Melsted, Pall ;
Pachter, Lior .
NATURE BIOTECHNOLOGY, 2016, 34 (05) :525-527
[8]   Expression of the SEPT9_i4 isoform confers resistance to microtubule-interacting drugs [J].
Chacko, Alex D. ;
McDade, Simon S. ;
Chanduloy, Severine ;
Church, Stewart W. ;
Kennedy, Richard ;
Price, John ;
Hall, Peter A. ;
Russell, S. E. Hilary .
CELLULAR ONCOLOGY, 2012, 35 (02) :85-93
[9]   A community effort to assess and improve drug sensitivity prediction algorithms [J].
Costello, James C. ;
Heiser, Laura M. ;
Georgii, Elisabeth ;
Gonen, Mehmet ;
Menden, Michael P. ;
Wang, Nicholas J. ;
Bansal, Mukesh ;
Ammad-ud-din, Muhammad ;
Hintsanen, Petteri ;
Khan, Suleiman A. ;
Mpindi, John-Patrick ;
Kallioniemi, Olli ;
Honkela, Antti ;
Aittokallio, Tero ;
Wennerberg, Krister ;
Collins, James J. ;
Gallahan, Dan ;
Singer, Dinah ;
Saez-Rodriguez, Julio ;
Kaski, Samuel ;
Gray, Joe W. ;
Stolovitzky, Gustavo .
NATURE BIOTECHNOLOGY, 2014, 32 (12) :1202-U57
[10]   Modeling precision treatment of breast cancer [J].
Daemen, Anneleen ;
Griffith, Obi L. ;
Heiser, Laura M. ;
Wang, Nicholas J. ;
Enache, Oana M. ;
Sanborn, Zachary ;
Pepin, Francois ;
Durinck, Steffen ;
Korkola, James E. ;
Griffith, Malachi ;
Hur, Joe S. ;
Huh, Nam ;
Chung, Jongsuk ;
Cope, Leslie ;
Fackler, Mary Jo ;
Umbricht, Christopher ;
Sukumar, Saraswati ;
Seth, Pankaj ;
Sukhatme, Vikas P. ;
Jakkula, Lakshmi R. ;
Lu, Yiling ;
Mills, Gordon B. ;
Cho, Raymond J. ;
Collisson, Eric A. ;
van't Veer, Laura J. ;
Spellman, Paul T. ;
Gray, Joe W. .
GENOME BIOLOGY, 2013, 14 (10)