Evidence map›Paper›PMID 33431933›Full record

ArticleScientific reports2021

Potentiality of multiple modalities for single-cell analyses to evaluate the tumor microenvironment in clinical specimens.

Yukie Kashima, Yosuke Togashi, Shota Fukuoka, Takahiro Kamada, Takuma Irie, Ayako Suzuki, Yoshiaki Nakamura, Kohei Shitara, Tatsunori Minamide, Taku Yoshida and 13 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Multiplatform Single-Cell Analysis Identifies Immune Cell Types Enhanced in Pulmonary Fibrosis.American journal of respiratory cell and molecular biology · 2022
    Article
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  16. CyTOFFrontiers in immunology · 2022
    Review
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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

23 authors at 6 institutions in 1 country.

Yukie KashimaDivision of Translational Genomics, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, 277-8577, Japan.
Yosuke TogashiDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Shota FukuokaDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Takahiro KamadaDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Takuma IrieDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Ayako SuzukiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, Japan.
Yoshiaki NakamuraDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, 277-8577, Japan.
Kohei ShitaraDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Chiba, 277-8577, Japan.
Tatsunori MinamideDepartment of Gastroenterology and Endoscopy, National Cancer Center Hospital East, Chiba, Japan.
Taku YoshidaDrug Discovery Research, Astellas Pharma, Inc., Ibaraki, Japan.
Naofumi TaokaDrug Discovery Research, Astellas Pharma, Inc., Ibaraki, Japan.
Tatsuya KawaseDrug Discovery Research, Astellas Pharma, Inc., Ibaraki, Japan.
Teiji WadaOncology Research Laboratories I, DaiichiSankyo. Co., Ltd., Tokyo, Japan.
Koichiro InakiBiomarker & Translational Research Department, DaiichiSankyo. Co., Ltd., Tokyo, Japan.
Masataka ChiharaOncology Research Laboratories I, DaiichiSankyo. Co., Ltd., Tokyo, Japan.
Yukihiko EbisunoTakeda Pharmaceutical Company Ltd., Fujisawa, Japan.
Sakiyo TsukamotoAxcelead Drug Discovery Partners Inc., Fujisawa, Japan.
Ryo FujiiAxcelead Drug Discovery Partners Inc., Fujisawa, Japan.
Akihiro OhashiDivision of Translational Genomics, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, 277-8577, Japan. aohashi@east.ncc.go.jp.
Yutaka SuzukiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba, Japan.
Katsuya TsuchiharaDivision of Translational Informatics, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Hiroyoshi NishikawaDivision of Cancer Immunology, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Chiba, Japan.
Toshihiko DoiExperimental Therapeutics, National Cancer Center Hospital East, Chiba, Japan. tdoi@east.ncc.go.jp.
Chiba Cancer Center · JPNational Cancer Center Hospital East · JPAstellas Pharma (Japan) · JPDaiichi-Sankyo (Japan) · JPThe University of Tokyo · JPTakeda (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell level analysis is powerful tool to assess the heterogeneity of cellular components in tumor microenvironments (TME). In this study, we investigated immune-profiles using the single-cell analyses of endoscopically- or surgically-resected tumors, and peripheral blood mononuclear cells from gastric cancer patients. Furthermore, we technically characterized two distinct platforms of the single-cell analysis; RNA-seq-based analysis (scRNA-seq), and mass cytometry-based analysis (CyTOF), both of which are broadly embraced technologies. Our study revealed that the scRNA-seq analysis could cover a broader range of immune cells of TME in the biopsy-resected small samples of tumors, detecting even small subgroups of B cells or Treg cells in the tumors, although CyTOF could distinguish the specific populations in more depth. These findings demonstrate that scRNA-seq analysis is a highly-feasible platform for elucidating the complexity of TME in small biopsy tumors, which would provide a novel strategies to overcome a therapeutic difficulties against cancer heterogeneity in TME.

Indexed as

Single-Cell AnalysisTumor MicroenvironmentAdultBiopsyFemaleHumansLeukocytes, MononuclearMaleMiddle AgedRNA-SeqStomach Neoplasms

Identifiers

PMID33431933
PMCPMC7801605
OpenAlexW3119943284

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.