Evidence map›Paper›PMID 31081058›Full record

ArticleInternational journal of oncology2019

Phospho‑STAT1 expression as a potential biomarker for anti‑PD‑1/anti‑PD‑L1 immunotherapy for breast cancer.

Yuko Nakayama, Kosaku Mimura, Tomoaki Tamaki, Kensuke Shiraishi, Ley-Fang Kua, Vivien Koh, Masato Ohmori, Ayako Kimura, Shingo Inoue, Hirokazu Okayama and 4 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 62 citations in OpenAlex.

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  8. Biomarker-oriented chemo-immunotherapy for advanced gastric cancer.International journal of clinical oncology · 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

14 authors at 4 institutions in 2 countries.

Yuko NakayamaFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Kosaku MimuraDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine, Fukushima, 960‑1295, Japan.
Tomoaki TamakiDepartment of Radiation Oncology, Fukushima Medical University School of Medicine, Fukushima, 960‑1295, Japan.
Kensuke ShiraishiFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Ley-Fang KuaNational University Cancer Institute, Singapore, National University Health System, Singapore 119228, Republic of Singapore.
Vivien KohNational University Cancer Institute, Singapore, National University Health System, Singapore 119228, Republic of Singapore.
Masato OhmoriFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Ayako KimuraFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Shingo InoueFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Hirokazu OkayamaDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine, Fukushima, 960‑1295, Japan.
Yoshiyuki SuzukiDepartment of Radiation Oncology, Fukushima Medical University School of Medicine, Fukushima, 960‑1295, Japan.
Tadao NakazawaDepartment of Pathology, University of Yamanashi, Yamanashi 409‑3898, Japan.
Daisuke IchikawaFirst Department of Surgery, University of Yamanashi, Yamanashi 409‑3898, Japan.
Koji KonoDepartment of Gastrointestinal Tract Surgery, Fukushima Medical University School of Medicine, Fukushima, 960‑1295, Japan.
University of Yamanashi · JPFukushima Medical University · JPNational University Cancer Institute, Singapore · SGNational University Health System · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, we evaluated the mechanisms of programmed death ligand 1 (PD‑L1) expression in the breast cancer microenvironment, focusing on the role of interferon‑γ (IFN‑γ), and the clinical indications for anti‑programmed cell death 1 (PD‑1) /anti‑PD‑L1 immunotherapy. We evaluated PD‑L1 expression in 4 breast cancer cell lines in the presence of 3 types of inhibitors, as well as IFN‑γ. The expression of phosphorylated signal transducer and activator of transcription 1 (p‑STAT1), one of the IFN‑γ signaling pathway molecules, was analyzed using immunohistochemistry (IHC) in relation to PD‑L1 and human leukocyte antigen (HLA) class I expression on cancer cells and tumor‑infiltrating CD8‑positive T cells in 111 patients with stage II/III breast cancer. Using The Cancer Genome Atlas (TCGA) database, the correlation of the IFN‑γ signature with PD‑L1 expression was analyzed in breast invasive carcinoma tissues. As a result, the JAK/STAT pathway via IFN‑γ was mainly involved in PD‑L1 expression in the cell lines examined. IHC analysis revealed that the PD‑L1 and HLA class I expression levels were significantly upregulated in the p‑STAT1‑positive cases. TCGA analysis indicated that the PD‑L1 expression and IFN‑γ signature exhibited a positive correlation. On the whole, these findings suggest that PD‑L1 and HLA class I are co‑expressed in p‑STAT1‑positive breast cancer cells induced by IFN‑γ secreted from tumor infiltrating immune cells, and that p‑STAT1 expression may be a potential biomarker for patient selection for immunotherapy with anti‑PD‑1/anti‑PD‑L1 monoclonal antibodies.

Indexed as

Up-RegulationAdultAgedAged, 80 and overB7-H1 AntigenBreast NeoplasmsCD8-Positive T-LymphocytesCell Line, TumorFemaleGene Expression Regulation, NeoplasticHistocompatibility Antigens Class IHumansImmunotherapyInterferon-gammaLymphocytes, Tumor-InfiltratingMCF-7 CellsB7-H1 AntigenCD274 protein, humanHistocompatibility Antigens Class IIFNG protein, humanInterferon-gammaSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID31081058
PMCPMC6521934
OpenAlexW2940236081

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.