Evidence map›Paper›PMID 34071865›Full record

ArticleCurrent issues in molecular biology2021

Renal Cell Carcinoma-Infiltrating CD3

Hye Won Lee, Chanho Park, Je-Gun Joung, Minyong Kang, Yun Shin Chung, Won Joon Oh, Seon-Yong Yeom, Woong-Yang Park, Tae Jin Kim, Seong Il Seo

Open access · goldAbstract read
In one paragraph

Article in Current issues in molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

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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

10 authors at 5 institutions in 1 country.

Hye Won LeeCenter for Urologic Cancer, National Cancer Center, Department of Urology, Goyang 10408, Korea.
Chanho ParkDepartment of Immunology, Sungkyunkwan University School of Medicine, Suwon 16419, Korea.
Je-Gun JoungDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.ORCID 0000-0003-2859-1036
Minyong KangSamsung Medical Center, Department of Urology, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Yun Shin ChungDepartment of Immunology, Sungkyunkwan University School of Medicine, Suwon 16419, Korea.ORCID 0000-0002-4971-486X
Won Joon OhDepartment of Immunology, Sungkyunkwan University School of Medicine, Suwon 16419, Korea.
Seon-Yong YeomSamsung Medical Center, Department of Urology, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Woong-Yang ParkDepartment of Health Science and Technology, Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Seoul 06351, Korea.ORCID 0000-0003-4234-0380
Tae Jin KimDepartment of Immunology, Sungkyunkwan University School of Medicine, Suwon 16419, Korea.
Seong Il SeoSamsung Medical Center, Department of Urology, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Sungkyunkwan University · KRSamsung Medical Center · KRCHA University · KRNational Cancer Center · KRSamsung (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the highly immunogenic nature of renal cell carcinoma (RCC), the tumor microenvironment (TME) is enriched with various innate and adaptive immune subsets. In particular, gamma-delta (γδ) T cells can act as potent attractive mediators of adoptive cell transfer immunotherapy because of their unique properties such as non-reliance on major histocompatibility complex expression, their ability to infiltrate human tumors and recognize tumor antigens, relative insensitivity to immune checkpoint molecules, and broad tumor cytotoxicity. Therefore, it is now critical to better characterize human γδ T-cell subsets and their mechanisms in RCCs, especially the stage of differentiation. In this study, we aimed to identify γδ T cells that might have adaptive responses against RCC progression. We characterized γδ T cells in peripheral blood and tumor-infiltrating lymphocytes (TILs) in freshly resected tumor specimens from 20 RCC patients. Furthermore, we performed a gene set enrichment analysis on RNA-sequencing data from The Cancer Genome Atlas (TCGA) derived from normal kidneys and RCC tumors to ascertain the association between γδ T-cell infiltration and anti-cancer immune activity. Notably, RCC-infiltrating CD3

Indexed as

AdultAgedAged, 80 and overCarcinoma, Renal CellCD3 ComplexCytokinesFemaleFlow CytometryGene Expression Regulation, NeoplasticHumansKidney NeoplasmsLymphocytes, Tumor-InfiltratingMaleMiddle AgedReceptors, Antigen, T-Cell, gamma-deltaRNA-SeqCD3 ComplexCytokinesReceptors, Antigen, T-Cell, gamma-deltaadoptive immunotherapyanti-tumor immunitygamma-delta T cellsrenal cell carcinomatumor-infiltrating lymphocytestumor microenvironment

Identifiers

PMID34071865
PMCPMC8929056
OpenAlexW3165019442

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.