Evidence map›Paper›PMID 37238964›Full record

ArticleBiomedicines2023

Initial Myeloid Cell Status Is Associated with Clinical Outcomes of Renal Cell Carcinoma.

Saima Sabrina, Yuji Takeda, Tomoyuki Kato, Sei Naito, Hiromi Ito, Yuki Takai, Masaki Ushijima, Takafumi Narisawa, Hidenori Kanno, Toshihiko Sakurai and 4 more

Abstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

14 authors.

Saima SabrinaDepartment of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0001-7203-2886
Yuji TakedaDepartment of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0002-0823-1802
Tomoyuki KatoDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Sei NaitoDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0002-6104-4344
Hiromi ItoDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Yuki TakaiDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Masaki UshijimaDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Takafumi NarisawaDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Hidenori KannoDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0001-9185-2134
Toshihiko SakuraiDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Shinichi SaitohDepartment of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0001-7523-8177
Akemi ArakiDepartment of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.
Norihiko TsuchiyaDepartment of Urology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0003-4242-2618
Hironobu AsaoDepartment of Immunology, Faculty of Medicine, Yamagata University, Yamagata 990-9585, Japan.ORCID 0000-0002-1051-4799

Funding

Grant-in-Aid for Scientific Research 17K11122
6 · The paper itself

Abstract

The therapeutic outcome of immune checkpoint inhibition (ICI) can be improved through combination treatments with ICI therapy. Myeloid-derived suppressor cells (MDSCs) strongly suppress tumor immunity. MDSCs are a heterogeneous cell population, originating from the unusual differentiation of neutrophils/monocytes induced by environmental factors such as inflammation. The myeloid cell population consists of an indistinguishable mixture of various types of MDSCs and activated neutrophils/monocytes. In this study, we investigated whether the clinical outcomes of ICI therapy could be predicted by estimating the status of the myeloid cells, including MDSCs. Several MDSC indexes, such as glycosylphosphatidylinositol-anchored 80 kD protein (GPI-80), CD16, and latency-associated peptide-1 (LAP-1; transforming growth factor-β1 precursor), were analyzed via flow cytometry using peripheral blood derived from patients with advanced renal cell carcinoma (

Indexed as

CD16glycosylphosphatidylinositol-anchored 80 kD proteinimmune checkpoint inhibitionlatency-associated peptide-1myeloid-derived suppressor cellsrenal cell carcinoma

Identifiers

PMID37238964
PMCPMC10216014

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Registered trials

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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.