Evidence map›Paper›PMID 36139078›Full record

ReviewBiomolecules2022

Research Progress on Nanoparticles-Based CRISPR/Cas9 System for Targeted Therapy of Tumors.

Dengyun Nie, Ting Guo, Miao Yue, Wenya Li, Xinyu Zong, Yinxing Zhu, Junxing Huang, Mei Lin

Abstract readReview
In one paragraph

Review in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Nature Inspired Delivery Vehicles for CRISPR-Based Genome Editing.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  5. Review
  6. Functional Genomics: Principles and Methods.Advances in experimental medicine and biology · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
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  14. 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

8 authors.

Dengyun NieTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Ting GuoTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Miao YueTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Wenya LiTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Xinyu ZongTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.ORCID 0000-0003-4438-8783
Yinxing ZhuTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Junxing HuangTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.
Mei LinTaizhou People's Hospital Affiliated to Nanjing University of Chinese Medicine, Taizhou 225300, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a genetic mutation disease that seriously endangers the health and life of all human beings. As one of the most amazing academic achievements in the past decade, CRISPR/Cas9 technology has been sought after by many researchers due to its powerful gene editing capability. CRISPR/Cas9 technology shows great potential in oncology, and has become one of the most promising technologies for cancer genome-editing therapeutics. However, its efficiency and the safety issues of in vivo gene editing severely limit its widespread application. Therefore, developing a suitable delivery method for the CRISPR/Cas9 system is an urgent problem to be solved at present. Rapid advances in nanomedicine suggest nanoparticles could be a viable option. In this review, we summarize the latest research on the potential use of nanoparticle-based CRISPR/Cas9 systems in cancer therapeutics, in order to further their clinical application. We hope that this review will provide a novel insight into the CRISPR/Cas9 system and offer guidance for nanocarrier designs that will enable its use in cancer clinical applications.

Indexed as

NanoparticlesNeoplasmsCRISPR-Cas SystemsGene EditingGenetic TherapyHumanscancerCRISPR/Cas9deliverynanoparticlestherapy

Identifiers

PMID36139078
PMCPMC9496048

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.