Evidence map›Paper›PMID 32329580›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2020

Active Delivery of VLPs Promotes Anti-Tumor Activity in a Mouse Ovarian Tumor Model.

Chao Wang, Berta Esteban Fernández de Ávila, Rodolfo Mundaca-Uribe, Miguel Angel Lopez-Ramirez, Doris E Ramírez-Herrera, Sourabh Shukla, Nicole F Steinmetz, Joseph Wang

Open access · greenAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Engineering Microbial Particles for Next-Generation Biomedical Platforms.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Micromotor-Enabled Active Hydrogen and Tobramycin Delivery for Synergistic Sepsis Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  10. Medical micro- and nanomotors in the body.Acta pharmaceutica Sinica. B · 2023
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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 at 1 institution in 1 country.

Chao WangDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Berta Esteban Fernández de ÁvilaDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Rodolfo Mundaca-UribeDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Miguel Angel Lopez-RamirezDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Doris E Ramírez-HerreraDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Sourabh ShuklaDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Nicole F SteinmetzDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Joseph WangDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.ORCID 0000-0002-4921-9674
University of California San Diego · US

Funding

Overcoming the immune-suppressive tumor microenvironment through in situ vaccination nanotechnology.U01CA218292 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIERING, STEVEN, STEINMETZ, NICOLE FRANZISKA · 2017 to 2021
$3.0M
NCI NIH HHS U01 CA218292
6 · The paper itself

Abstract

Virus-like nanoparticles (VLPs) have been used as an attractive means in cancer immunotherapy because of their unique intrinsic immunostimulatory properties. However, for treating metastatic tumors in the peritoneal cavity, such as ovarian cancer, multiple injections of therapy are needed due to the large peritoneal space and fast excretion of therapy. Here, it is reported on the development of active VLP delivery vehicles for the treatment of peritoneal ovarian tumors using biocompatible Qβ VLPs-loaded Mg-based micromotors. The autonomous propulsion of such Qβ VLPs-loaded Mg-micromotors in the peritoneal fluid enables active delivery of intact immunostimulatory Qβ VLPs to the peritoneal space of ovarian tumor bearing mice, greatly enhancing the local distribution and retention of Qβ VLPs. Such improved distribution and longer retention time of Qβ in the peritoneal cavity leads to enhanced immunostimulation and therefore increased survival rate of tumor-bearing mice compared to a passive Qβ treatment. For clinical translation, the active delivery of VLPs holds great promise for tumor immunotherapy toward the treatment of different types of primary and metastatic tumors in the peritoneal cavity.

Indexed as

Ovarian NeoplasmsAnimalsFemaleHumansImmunizationImmunotherapyMiceSurvival Rateactive deliveryimmunotherapymicromotorsovarian tumorsvirus-like particles

Identifiers

PMID32329580
PMCPMC7507763
OpenAlexW3019066444

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.