Correlation Engine 2.0
Clear Search sequence regions


  • CDK5 (1)
  • humans (1)
  • paclitaxel (1)
  • PBRM1 (1)
  • RSF1 (1)
  • SGOL1 (1)
  • SLFN11 (1)
  • sorafenib (1)
  • strand breaks (1)
  • Sizes of these terms reflect their relevance to your search.

    In this review, we focus on the application of clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated nuclease 9 (Cas9), as a powerful genome editing system, in the identification of resistance mechanisms and in overcoming drug resistance in the most frequent solid tumors. Data were collected by conducting systematic searching of scientific English literature using specific keywords such as "cancer", "CRISPR" and related combinations. The review findings revealed the importance of CRISPR/Cas9 system in understanding drug resistance mechanisms and identification of resistance-related genes such as PBRM1, SLFN11 and ATPE1 in different cancers. We also provided an overview of genes, including RSF1, CDK5, and SGOL1, whose disruption can synergize with the currently available drugs such as paclitaxel and sorafenib. The data suggest CRISPR/Cas9 system as a useful tool in elucidating the molecular basis of drug resistance and improving clinical outcomes. Graphical abstract The mechanisms of CRISPR/Cas9-mediated genome editing and double-strand breaks (DSBs) repair.

    Citation

    Ali Saber, Bin Liu, Pirooz Ebrahimi, Hidde J Haisma. CRISPR/Cas9 for overcoming drug resistance in solid tumors. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences. 2020 Jun;28(1):295-304

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 30666557

    View Full Text