Evidence map›Paper›PMID 36200687›Full record

ArticleCancer medicine2023

Cisplatin-induced HSF1-HSP90 axis enhances the expression of functional PD-L1 in oral squamous cell carcinoma.

Takashi Sasaya, Terufumi Kubo, Kenji Murata, Yuka Mizue, Kenta Sasaki, Junko Yanagawa, Makoto Imagawa, Hirotaka Kato, Tomohide Tsukahara, Takayuki Kanaseki and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Afatinib exerts an inhibitory effect on T cell-mediated cytotoxicity.Cancer immunology, immunotherapy : CII · 2026
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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 1 institution in 1 country.

Takashi SasayaDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Terufumi KuboDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.ORCID 0000-0001-9274-2551
Kenji MurataDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Yuka MizueDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Kenta SasakiDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Junko YanagawaDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Makoto ImagawaDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Hirotaka KatoDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Tomohide TsukaharaDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.ORCID 0000-0002-3678-4359
Takayuki KanasekiDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.ORCID 0000-0001-7294-6880
Yasuaki TamuraDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Akihiro MiyazakiDepartment of Oral Surgery, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Yoshihiko HirohashiDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Toshihiko TorigoeDepartment of Pathology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitor-based cancer immunotherapy has provided an additional therapeutic option for oral squamous cell carcinoma (OSCC) with recurrence or distant metastases. However, further improvement of OSCC treatment is required to develop the optimal combination or order for chemoradiotherapy and immunotherapy. Along with the accumulation of clinical knowledge and evidence, it is also essential to clarify the biological impact of chemo-radiotherapeutic agents on the cancer immune microenvironment. In this study, we investigated the effects of cisplatin (CDDP), a key therapeutic agent for OSCC, on programmed death-ligand 1 (PD-L1) expression in OSCC lines. Although CDDP treatment increased the surface levels of PD-L1 on OSCC cell lines, the gene and total protein expression levels of PD-L1 were not altered. We also demonstrated that the phosphorylation of heat shock factor 1 and heat shock protein 90 was involved in this process. In addition, CDDP-induced PD-L1 attenuated the target-specific cytotoxic T lymphocyte reaction to OSCC. These results provide an immunobiological basis for the response of OSCC to CDDP and will contribute to our biological understanding of the action of novel combination therapy including immunotherapy together with platinum-based chemotherapy for OSCC.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsB7-H1 AntigenCisplatinHumansSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanCisplatincisplatinheat shock factor 1heat shock protein 90oral squamous cell carcinomaPD-L1

Identifiers

PMID36200687
PMCPMC9972142
OpenAlexW4302303967

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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.