Genome-wide CRISPR screens reveal synthetic lethality of RNASEH2 deficiency and ATR inhibition

scientific article published on 07 December 2018

Genome-wide CRISPR screens reveal synthetic lethality of RNASEH2 deficiency and ATR inhibition is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1038/S41388-018-0606-4
P932PMC publication ID6450769
P698PubMed publication ID30532030

P2093author name stringJie Zhang
Junjie Chen
Nora M Navone
Chao Wang
Zhen Chen
Gang Wang
Xu Feng
Mengfan Tang
Mrinal Srivastava
Peter Shepherd
Megan E McLaughlin
Glen Traver Hart
P2860cites workMED12 controls the response to multiple cancer drugs through regulation of TGF-β receptor signalingQ24304423
RNase H2 roles in genome integrity revealed by unlinking its activitiesQ27676027
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Targeted disruption of the cell-cycle checkpoint gene ATR leads to early embryonic lethality in miceQ28143813
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ATR disruption leads to chromosomal fragmentation and early embryonic lethalityQ28591433
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RNaseH2 mutants that cause Aicardi-Goutieres syndrome are active nucleasesQ33779326
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Reduction of hRNase H2 activity in Aicardi-Goutières syndrome cells leads to replication stress and genome instabilityQ34920730
AGS, SLE, and RNASEH2 mutations: translating insights into therapeutic advancesQ35242554
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities.Q35858015
SLFN11 inhibits checkpoint maintenance and homologous recombination repairQ35866775
BAGEL: a computational framework for identifying essential genes from pooled library screens.Q35991327
Bridging the gap between in vitro and in vivo: Dose and schedule predictions for the ATR inhibitor AZD6738Q35999359
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Protein kinase mutants of human ATR increase sensitivity to UV and ionizing radiation and abrogate cell cycle checkpoint controlQ36490482
Targeting ATR in vivo using the novel inhibitor VE-822 results in selective sensitization of pancreatic tumors to radiation.Q36525188
RNase H2 catalytic core Aicardi-Goutières syndrome-related mutant invokes cGAS-STING innate immune-sensing pathway in mice.Q36745063
Ribonuclease H2 mutations induce a cGAS/STING-dependent innate immune responseQ36866528
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndrome.Q37022007
Pathological ribonuclease H1 causes R-loop depletion and aberrant DNA segregation in mitochondriaQ37142690
A Genome-wide CRISPR Screen Identifies CDC25A as a Determinant of Sensitivity to ATR InhibitorsQ37268724
Substantial interindividual and limited intraindividual genomic diversity among tumors from men with metastatic prostate cancerQ37302524
ATR inhibitors as a synthetic lethal therapy for tumours deficient in ARID1A.Q37508792
The essential kinase ATR: ensuring faithful duplication of a challenging genome.Q38622938
Evaluation and Design of Genome-Wide CRISPR/SpCas9 Knockout Screens.Q38706202
Genome-wide CRISPR screens reveal a Wnt-FZD5 signaling circuit as a druggable vulnerability of RNF43-mutant pancreatic tumorsQ38729876
Targeting the ATR-CHK1 Axis in Cancer TherapyQ38817102
Measuring error rates in genomic perturbation screens: gold standards for human functional genomicsQ38978817
ATR pathway inhibition is synthetically lethal in cancer cells with ERCC1 deficiencyQ39012252
The impact of replication stress on replication dynamics and DNA damage in vertebrate cells.Q39438600
Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR.Q39559122
Discovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents.Q42745810
Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagyQ46289705
Genome-Wide CRISPR/Cas9 Screening for High-Throughput Functional Genomics in Human Cells.Q47951609
The role of RNase H2 in processing ribonucleotides incorporated during DNA replication.Q50212840
ATR inhibition induces synthetic lethality and overcomes chemoresistance in TP53- or ATM-defective chronic lymphocytic leukemia cellsQ50913049
Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer ModelsQ52811875
Methylation of SLFN11 is a marker of poor prognosis and cisplatin resistance in colorectal cancerQ52881647
Integrative Clinical Genomics of Advanced Prostate CancerQ53788627
CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesionsQ59084697
The cGAS-cGAMP-STING pathway connects DNA damage to inflammation, senescence, and cancerQ88286449
P433issue14
P407language of work or nameEnglishQ1860
P921main subjectCRISPRQ412563
P304page(s)2451-2463
P577publication date2018-12-07
P1433published inOncogeneQ1568657
P1476titleGenome-wide CRISPR screens reveal synthetic lethality of RNASEH2 deficiency and ATR inhibition
P478volume38

Reverse relations

cites work (P2860)
Q90042293A consensus set of genetic vulnerabilities to ATR inhibition
Q102140719Beyond Kinases: Targeting Replication Stress Proteins in Cancer Therapy
Q92540221Chemogenetic interactions in human cancer cells
Q92992933Control of homologous recombination by the HROB-MCM8-MCM9 pathway
Q91999877Genome-wide CRISPR screen uncovers a synergistic effect of combining Haspin and Aurora kinase B inhibition
Q90428476High density of unrepaired genomic ribonucleotides leads to Topoisomerase 1-mediated severe growth defects in absence of ribonucleotide reductase
Q92787848Identifying chemogenetic interactions from CRISPR screens with drugZ
Q95940288Integrative analysis of large-scale loss-of-function screens identifies robust cancer-associated genetic interactions
Q96302601MCM8IP activates the MCM8-9 helicase to promote DNA synthesis and homologous recombination upon DNA damage
Q91944953Molecular and physiological consequences of faulty eukaryotic ribonucleotide excision repair
Q89759382Val143 of human ribonuclease H2 is not critical for, but plays a role in determining catalytic activity and substrate specificity

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