Evidence map›Paper›PMID 37409429›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2023

Genetically Engineered-Cell-Membrane Nanovesicles for Cancer Immunotherapy.

Qinzhen Cheng, Yong Kang, Bin Yao, Jinrui Dong, Yalan Zhu, Yiling He, Xiaoyuan Ji

Abstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Biomimetic Cell Membrane-Coated MOFs System for Targeted Cancer Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  11. Review
  12. Article
  13. Review
  14. Bioactive materials · 2025
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
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

7 authors.

Qinzhen ChengJinhua Municipal Central Hospital, Jinhua, 321000, China.
Yong KangAcademy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.
Bin YaoAcademy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.
Jinrui DongAcademy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.
Yalan ZhuJinhua Municipal Central Hospital, Jinhua, 321000, China.
Yiling HeJinhua Municipal Central Hospital, Jinhua, 321000, China.
Xiaoyuan JiAcademy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.ORCID 0000-0002-6768-2304

Funding

National Natural Science Foundation of China 32071322National Natural Science Funds for Excellent Young Scholar 32122044Technology & Innovation Commission of Shenzhen Municipality JCYJ20210324113004010
6 · The paper itself

Abstract

The advent of immunotherapy has marked a new era in cancer treatment, offering significant clinical benefits. Cell membrane as drug delivery materials has played a crucial role in enhancing cancer therapy because of their inherent biocompatibility and negligible immunogenicity. Different cell membranes are prepared into cell membrane nanovesicles (CMNs), but CMNs have limitations such as inefficient targeting ability, low efficacy, and unpredictable side effects. Genetic engineering has deepened the critical role of CMNs in cancer immunotherapy, enabling genetically engineered-CMN (GCMN)-based therapeutics. To date, CMNs that are surface modified by various functional proteins have been developed through genetic engineering. Herein, a brief overview of surface engineering strategies for CMNs and the features of various membrane sources is discussed, followed by a description of GCMN preparation methods. The application of GCMNs in cancer immunotherapy directed at different immune targets is addressed as are the challenges and prospects of GCMNs in clinical translation.

Indexed as

Drug Delivery SystemsNeoplasmsCell MembraneGenetic EngineeringImmunotherapycancer immunotherapycell membrane nanovesicles (CMNs)genetically engineered-cell-membrane nanovesicles (GCMNs)genetic engineeringimmune targets

Identifiers

PMID37409429
PMCPMC10502869

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.