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Discovery of synthetic lethal interactions from large-scale pan-cancer perturbation screens

Author

Listed:
  • Sumana Srivatsa

    (ETH Zurich
    SIB Swiss Institute of Bioinformatics)

  • Hesam Montazeri

    (University of Tehran)

  • Gaia Bianco

    (University of Basel)

  • Mairene Coto-Llerena

    (University of Basel
    University Hospital Basel)

  • Mattia Marinucci

    (University of Basel)

  • Charlotte K. Y. Ng

    (SIB Swiss Institute of Bioinformatics
    University of Bern)

  • Salvatore Piscuoglio

    (University of Basel
    University Hospital Basel)

  • Niko Beerenwinkel

    (ETH Zurich
    SIB Swiss Institute of Bioinformatics)

Abstract

The development of cancer therapies is limited by the availability of suitable drug targets. Potential candidate drug targets can be identified based on the concept of synthetic lethality (SL), which refers to pairs of genes for which an aberration in either gene alone is non-lethal, but co-occurrence of the aberrations is lethal to the cell. Here, we present SLIdR (Synthetic Lethal Identification in R), a statistical framework for identifying SL pairs from large-scale perturbation screens. SLIdR successfully predicts SL pairs even with small sample sizes while minimizing the number of false positive targets. We apply SLIdR to Project DRIVE data and find both established and potential pan-cancer and cancer type-specific SL pairs consistent with findings from literature and drug response screening data. We experimentally validate two predicted SL interactions (ARID1A-TEAD1 and AXIN1-URI1) in hepatocellular carcinoma, thus corroborating the ability of SLIdR to identify potential drug targets.

Suggested Citation

  • Sumana Srivatsa & Hesam Montazeri & Gaia Bianco & Mairene Coto-Llerena & Mattia Marinucci & Charlotte K. Y. Ng & Salvatore Piscuoglio & Niko Beerenwinkel, 2022. "Discovery of synthetic lethal interactions from large-scale pan-cancer perturbation screens," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-35378-z
    DOI: 10.1038/s41467-022-35378-z
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    as
    1. Joo Sang Lee & Avinash Das & Livnat Jerby-Arnon & Rand Arafeh & Noam Auslander & Matthew Davidson & Lynn McGarry & Daniel James & Arnaud Amzallag & Seung Gu Park & Kuoyuan Cheng & Welles Robinson & Di, 2018. "Harnessing synthetic lethality to predict the response to cancer treatment," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    2. Michael S. Lawrence & Petar Stojanov & Paz Polak & Gregory V. Kryukov & Kristian Cibulskis & Andrey Sivachenko & Scott L. Carter & Chip Stewart & Craig H. Mermel & Steven A. Roberts & Adam Kiezun & Pe, 2013. "Mutational heterogeneity in cancer and the search for new cancer-associated genes," Nature, Nature, vol. 499(7457), pages 214-218, July.
    3. Michael S. Lawrence & Petar Stojanov & Craig H. Mermel & James T. Robinson & Levi A. Garraway & Todd R. Golub & Matthew Meyerson & Stacey B. Gabriel & Eric S. Lander & Gad Getz, 2014. "Discovery and saturation analysis of cancer genes across 21 tumour types," Nature, Nature, vol. 505(7484), pages 495-501, January.
    4. Nicola A. Thompson & Marco Ranzani & Louise Weyden & Vivek Iyer & Victoria Offord & Alastair Droop & Fiona Behan & Emanuel Gonçalves & Anneliese Speak & Francesco Iorio & James Hewinson & Victoria Har, 2021. "Combinatorial CRISPR screen identifies fitness effects of gene paralogues," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
    5. Jordi Barretina & Giordano Caponigro & Nicolas Stransky & Kavitha Venkatesan & Adam A. Margolin & Sungjoon Kim & Christopher J.Wilson & Joseph Lehár & Gregory V. Kryukov & Dmitriy Sonkin & Anupama Red, 2012. "Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity," Nature, Nature, vol. 492(7428), pages 290-290, December.
    6. Jordi Barretina & Giordano Caponigro & Nicolas Stransky & Kavitha Venkatesan & Adam A. Margolin & Sungjoon Kim & Christopher J. Wilson & Joseph Lehár & Gregory V. Kryukov & Dmitriy Sonkin & Anupama Re, 2012. "The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity," Nature, Nature, vol. 483(7391), pages 603-607, March.
    7. Sekhon, Jasjeet S., 2011. "Multivariate and Propensity Score Matching Software with Automated Balance Optimization: The Matching package for R," Journal of Statistical Software, Foundation for Open Access Statistics, vol. 42(i07).
    8. Lei Chang & Luca Azzolin & Daniele Di Biagio & Francesca Zanconato & Giusy Battilana & Romy Lucon Xiccato & Mariaceleste Aragona & Stefano Giulitti & Tito Panciera & Alessandro Gandin & Gianluca Sigis, 2018. "The SWI/SNF complex is a mechanoregulated inhibitor of YAP and TAZ," Nature, Nature, vol. 563(7730), pages 265-269, November.
    9. Ewa Szczurek & Niko Beerenwinkel, 2014. "Modeling Mutual Exclusivity of Cancer Mutations," PLOS Computational Biology, Public Library of Science, vol. 10(3), pages 1-12, March.
    10. Peter C. DeWeirdt & Annabel K. Sangree & Ruth E. Hanna & Kendall R. Sanson & Mudra Hegde & Christine Strand & Nicole S. Persky & John G. Doench, 2020. "Genetic screens in isogenic mammalian cell lines without single cell cloning," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
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