Evidence map›Paper›PMID 39831754›Full record

ReviewCancer biology & medicine2025

Improving systemic delivery of oncolytic virus by cellular carriers.

Ziyi Peng, Muhammad Kalim, Yong Lu

Abstract readReview
In one paragraph

Review in Cancer biology & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. 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

3 authors.

Ziyi Peng *Houston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Muhammad Kalim *Houston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.
Yong LuHouston Methodist Cancer Center/Weill Cornell Medicine, Houston, TX 77030, USA.ORCID 0009-0001-4250-7278

Funding

Induction of autosis to overcome resistance in adoptive cell therapy for solid tumorsR01CA278911 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Yong Lu · 2023 to 2026
$2.3M
The Unique Roles of Tumor-Specific Th9 Cells for Solid Tumor EradicationR01CA258477 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
Eradication of Escaped Variant Tumor Cells for Cancer ImmunotherapyR01CA248111 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2021 to 2025
$1.9M
P38 MAPK is a molecular switch that controls the acquired resistance in adoptive cell therapyR37CA251318 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LU, YONG · 2020 to 2024
$1.8M
Decoupling acute toxicities and antitumor efficacy in adoptive cell therapyR01CA288403 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Yong Lu · 2024 to 2026
$1.8M
CPRIT Scholar Award RR210067NCI NIH HHS 1R01CA248111-01A1NCI NIH HHS 1R37CA251318-01NCI NIH HHS R01 CA248111NCI NIH HHS R01 CA258477NCI NIH HHS R01CA258477-01NCI NIH HHS R01 CA278911NCI NIH HHS R01CA278911NCI NIH HHS R01 CA288403NCI NIH HHS R01CA288403NCI NIH HHS R37 CA251318
6 · The paper itself

Abstract

Oncolytic virotherapy (OVT) is a promising option for cancer treatment. OVT involves selective oncolytic virus (OV) replication within cancer cells, which triggers anti-tumor responses and immunostimulation. Despite promising potential, OVT faces critical challenges, including insufficient tumor-specific targeting, which results in limited tumor penetration and variability in therapeutic efficacy. These challenges are particularly pronounced in solid tumors with complex microenvironments and heterogeneous vascularization. A comprehensive research program is currently underway to develop and refine innovative delivery methods to address these issues to enhance OVT precision and efficacy. A principal area of investigation is the utilization of cellular carriers to enhance the delivery and distribution of OVs within tumor microenvironments, thereby optimizing immune system activation and maximizing anti-tumor effects. This review offers a comprehensive overview of the current strategies that are being used to enhance the delivery of OVs via cellular carriers with the goal of improving the clinical impact of OVT in cancer therapy.

Indexed as

NeoplasmsOncolytic VirotherapyOncolytic VirusesAnimalsHumansTumor Microenvironmentcellular carriersOncolytic virotherapyoncolytic virussystemic deliverytumor-specific targeting

Identifiers

PMID39831754
PMCPMC11745088

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.