Evidence map›Paper›PMID 39760460›Full record

ArticleIntegrative cancer therapies

Rhus Verniciflua Stokes Inhibits PD-1 Expression and Induces Anticancer Effects by Enhancing T Cell Function.

Seoyoung Kim, Young-Kwan Lee, Wang-Jun Lee, Hyoun Jong Moon, Sanghun Lee

Abstract read
In one paragraph

Article in Integrative cancer therapies. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

5 authors.

Seoyoung KimEutilex Co. Ltd., Geumcheon-gu, Seoul, Republic of Korea.
Young-Kwan LeeExcelsisbio Inc., Goyang-si, Gyeonggi-do, Republic of Korea.
Wang-Jun LeeMyongji Hospital, Goyang-si, Gyeonggi-do, Republic of Korea.
Hyoun Jong MoonMyongji Hospital, Goyang-si, Gyeonggi-do, Republic of Korea.
Sanghun LeeMyongji Hospital, Goyang-si, Gyeonggi-do, Republic of Korea.ORCID 0000-0002-0573-9555

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver the last decade, the anticancer effects of

methodsPeripheral blood mononuclear cells (PBMCs) from breast cancer patients were isolated to obtain cytokine-induced killer cell populations with >85% CD3+ T cells. The anticancer activity of these T cells was evaluated by introducing red fluorescent protein (RFP) into HLA-A02:01 type-matched breast cancer cell lines (MCF7 and MDA-MB-231) and analyzing the results using flow cytometry. The effect of RVS extracts on T cell phenotype was assessed using markers such as CTLA-4 and PD-1, as well as mRNA expression levels of key genes (IFN-γ, TNF-α, and IL-2).

resultsRVS treatment significantly enhanced the anticancer activity of T cells against breast cancer cells. Specifically, T cells treated with 100 µg/mL of RVS showed a 20.6% increase in cytotoxicity against MCF-7 cells and a 36.2% increase against MDA-MB231 cells compared to the control. Additionally, RVS treatment led to a significant reduction in PD-1 expression on T cells.

conclusionOur findings demonstrate that RVS treatment enhances T cell function against breast cancer cells by reducing PD-1 expression. These results suggest that components of RVS may serve as potential candidates for restoring exhausted T cells in cancer therapy.

Indexed as

Breast NeoplasmsPlant ExtractsProgrammed Cell Death 1 ReceptorRhusT-LymphocytesCell Line, TumorCTLA-4 AntigenFemaleHumansInterferon-gammaInterleukin-2Leukocytes, MononuclearMCF-7 CellsCTLA-4 AntigenInterferon-gammaInterleukin-2PDCD1 protein, humanPlant ExtractsProgrammed Cell Death 1 Receptoranticancerbreast cancerimmuno-oncologyPD-1Rhus verniciflua StokesT cell co-culture

Identifiers

PMID39760460
PMCPMC11705362

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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.