Evidence map›Paper›PMID 27453044›Full record

ArticleMolecular cell2016

CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations.

Alexis Guernet, Sathish Kumar Mungamuri, Dorthe Cartier, Ravi Sachidanandam, Anitha Jayaprakash, Sahil Adriouch, Myriam Vezain, Françoise Charbonnier, Guy Rohkin, Sophie Coutant and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
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  7. Clonal tracking in cancer and metastasis.Cancer metastasis reviews · 2024
    Review
  8. Review
  9. Review
  10. Applications and advancements of CRISPR-Cas in the treatment of lung cancer.Frontiers in cell and developmental biology · 2023
    Review
  11. Review
  12. Review
  13. CRISPR in cancer biology and therapy.Nature reviews. Cancer · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 2 countries.

Alexis GuernetNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
Sathish Kumar MungamuriDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Dorthe CartierNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
Ravi SachidanandamDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Anitha JayaprakashDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sahil AdriouchInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Flow Cytometry and Cell Sorting Facility, 76000 Rouen, France.
Myriam VezainInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Genomics Facility,76000 Rouen, France.
Françoise CharbonnierInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Genomics Facility,76000 Rouen, France.
Guy RohkinDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sophie CoutantInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Genomics Facility,76000 Rouen, France.
Shen YaoDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Hassan AinaniNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
David AlexandreNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
Isabelle TournierInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Genomics Facility,76000 Rouen, France.
Olivier BoyerInstitute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France; IRIB Flow Cytometry and Cell Sorting Facility, 76000 Rouen, France; Department of Immunology, CHU Rouen, 76000 Rouen, France.
Stuart A AaronsonDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Youssef AnouarNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
Luca GrumolatoNormandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France. Electronic address: luca.grumolato@univ-rouen.fr.
Institute for Research and Innovation in Biomedicine · FRIcahn School of Medicine at Mount Sinai · USUniversité de Rouen Normandie · FRInserm · FRNormandie Université · FR

Funding

PW1--A mediator of cell survival by NFKB and cell death by p53P01CA080058 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI AARONSON, STUART A · 2000 to 2016
$20.2M
NCI NIH HHS P01 CA080058
6 · The paper itself

Abstract

Intratumor genetic heterogeneity underlies the ability of tumors to evolve and adapt to different environmental conditions. Using CRISPR/Cas9 technology and specific DNA barcodes, we devised a strategy to recapitulate and trace the emergence of subpopulations of cancer cells containing a mutation of interest. We used this approach to model different mechanisms of lung cancer cell resistance to EGFR inhibitors and to assess effects of combined drug therapies. By overcoming intrinsic limitations of current approaches, CRISPR-barcoding also enables investigation of most types of genetic modifications, including repair of oncogenic driver mutations. Finally, we used highly complex barcodes inserted at a specific genome location as a means of simultaneously tracing the fates of many thousands of genetically labeled cancer cells. CRISPR-barcoding is a straightforward and highly flexible method that should greatly facilitate the functional investigation of specific mutations, in a context that closely mimics the complexity of cancer.

Indexed as

CRISPR-Cas SystemsGenetic HeterogeneityOncogenesPoint MutationAnimalsAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell LineageClone CellsDNA Mutational AnalysisDNA, NeoplasmDose-Response Relationship, DrugDrug Resistance, NeoplasmErbB ReceptorsGene EditingBiomarkers, TumorDNA, NeoplasmEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitors

Identifiers

PMID27453044
PMCPMC5537739
OpenAlexW2479770185

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.