Evidence map›Paper›PMID 36703992›Full record

ArticleFrontiers in immunology2022

Natural killer cell therapy potentially enhances the antitumor effects of bevacizumab plus irinotecan in a glioblastoma mouse model.

Thi-Anh-Thuy Tran, Young-Hee Kim, Thi-Hoang-Oanh Duong, JayaLakshmi Thangaraj, Tan-Huy Chu, Shin Jung, In-Young Kim, Kyung-Sub Moon, Young-Jin Kim, Tae-Kyu Lee and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

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  9. Advances in tumor vascular growth inhibition.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

16 authors at 2 institutions in 1 country.

Thi-Anh-Thuy TranBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Young-Hee KimBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Thi-Hoang-Oanh DuongBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
JayaLakshmi ThangarajResearch Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Tan-Huy ChuResearch Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Shin JungBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
In-Young KimBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Kyung-Sub MoonBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Young-Jin KimBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Tae-Kyu LeeBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Chul Won LeeDepartment of Chemistry, Chonnam National University, Gwangju, Republic of Korea.
Hyosuk YunDepartment of Chemistry, Chonnam National University, Gwangju, Republic of Korea.
Je-Jung LeeResearch Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Hyun-Ju LeeResearch Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Kyung-Hwa LeeDepartment of Pathology, Chonnam National University Medical School, and Hwasun Hospital, Hwasun, Republic of Korea.
Tae-Young JungBrain Tumor Research Laboratory, Chonnam National University Hwasun Hospital, Hwasun, Republic of Korea.
Chonnam National University Hwasun Hospital · KRChonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various combination treatments have been considered to attain the effective therapy threshold by combining independent antitumor mechanisms against the heterogeneous characteristics of tumor cells in malignant brain tumors. In this study, the natural killer (NK) cells associated with bevacizumab (Bev) plus irinotecan (Iri) against glioblastoma multiforme (GBM) were investigated. For the experimental design, NK cells were expanded and activated by K562 cells expressing the OX40 ligand and membrane-bound IL-18 and IL-21. The effects of Bev and Iri on the proliferation and NK ligand expression of GBM cells were evaluated through MTT assay and flow cytometry. The cytotoxic effects of NK cells against Bev plus Iri-treated GBM cells were also predicted

Indexed as

Antineoplastic AgentsGlioblastomaAnimalsBevacizumabHumansIrinotecanKiller Cells, NaturalLigandsMiceMice, Inbred NODMice, SCIDAntineoplastic AgentsBevacizumabIrinotecanLigandsbevacizumabglioblastomairinotecannatural killer cellsU87 cell line

Identifiers

PMID36703992
PMCPMC9871756
OpenAlexW4315433897

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.