Evidence map›Paper›PMID 34745851›Full record

ReviewActa pharmaceutica Sinica. B2021

CRISPR-Cas9: A method for establishing rat models of drug metabolism and pharmacokinetics.

Jian Lu, Jie Liu, Yuanqing Guo, Yuanjin Zhang, Yeye Xu, Xin Wang

Abstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Harnessing the evolving CRISPR/Cas9 for precision oncology.Journal of translational medicine · 2024
    Review
  7. Construction and characterization of a humanizedActa pharmaceutica Sinica. B · 2024
    Article
  8. Article
  9. Recombinant Technologies Facilitate Drug Metabolism, Pharmacokinetics, and General Biomedical Research.Drug metabolism and disposition: the biological fate of chemicals · 2023
    Review
  10. Review
  11. Review
  12. Pleiotropic effects of DCLK1 in cancer and cancer stem cells.Frontiers in molecular biosciences · 2022
    Review
  13. Assessing cytochrome P450 function using genetically engineered mouse models.Advances in pharmacology (San Diego, Calif.) · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jian LuChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
Jie LiuChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
Yuanqing GuoChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
Yuanjin ZhangChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
Yeye XuChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.
Xin WangChangning Maternity and Infant Health Hospital, East China Normal University, Shanghai 200051, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 2020 Nobel Prize in Chemistry recognized CRISPR-Cas9, a super-selective and precise gene editing tool. CRISPR-Cas9 has an obvious advantage in editing multiple genes in the same cell, and presents great potential in disease treatment and animal model construction. In recent years, CRISPR-Cas9 has been used to establish a series of rat models of drug metabolism and pharmacokinetics (DMPK), such as

Indexed as

AAV, adeno-associated virusADMET, absorption, distribution, metabolism, excretion and toxicityAnimal modelBSEP, bile salt export pumpCRISPR-Cas9CRISPR-Cas, clustered regularly interspaced short palindromic repeats-CRISPR-associatedcrRNAs, CRISPR RNAsDDI, drug–drug interactionDMPK, drug metabolism and pharmacokineticsDrug metabolismDSB, double-strand breakGene editingHBV, hepatitis B virusHDR, homology directed repairHIV, human immunodeficiency virusHPV, human papillomavirusesKO, knockoutNCBI, National Center for Biotechnology InformationNHEJ, non-homologous end joiningOATP1B, organic anion transporting polypeptides 1BOTS, off-target sitePAM, protospacer-associated motifPharmacokineticspre-crRNA, pre-CRISPR RNARNP, ribonucleoproteinSD, Sprague–DawleysgRNA, single guide RNASREBP-2, sterol regulatory element-binding protein 2T7E I, T7 endonuclease ITALEN, transcriptional activators like effector nucleasesTALE, transcriptional activator-like effectortracRNA, trans-activating crRNAWT, wild-typeZFN, zinc finger nucleases

Identifiers

PMID34745851
PMCPMC8551406

What OpenQuestion holds

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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.