Evidence map›Paper›PMID 34502561›Full record

ArticleInternational journal of molecular sciences2021

Application of Immunoprofiling Using Multiplexed Immunofluorescence Staining Identifies the Prognosis of Patients with High-Grade Serous Ovarian Cancer.

Shin-Wha Lee, Ha-Young Lee, Sung Wan Kang, Min Je Kim, Young-Jae Lee, Chang Ohk Sung, Yong-Man Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. High density and proximity of CD8Thoracic cancer · 2023
    Article
  5. Review
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

7 authors at 2 institutions in 1 country.

Shin-Wha LeeDepartment of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.ORCID 0000-0002-5088-1905
Ha-Young LeeAsan Institute for Life Science, Seoul 05505, Korea.
Sung Wan KangAsan Institute for Life Science, Seoul 05505, Korea.ORCID 0000-0002-7360-8311
Min Je KimAsan Institute for Life Science, Seoul 05505, Korea.
Young-Jae LeeDepartment of Obstetrics and Gynecology, GangNeung Asan Hospital, University of Ulsan College of Medicine, Gangneung 25440, Korea.
Chang Ohk SungDepartment of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Yong-Man KimDepartment of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Ulsan College · KRAsan Medical Center · KR

Funding

Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea 2016-588 & 2016-731
6 · The paper itself

Abstract

Immunoprofiling has an established impact on the prognosis of several cancers; however, its role and definition in high-grade serous ovarian cancer (HGSOC) are mostly unknown. This study is to investigate immunoprofiling which could be a prognostic factor in HGSOC. We produced tumor microarrays of 187 patients diagnosed with HGSOC. We performed a multiplexed immunofluorescence staining using Opal Multiplex IHC kit and quantitative analysis with Vectra-Inform system. The expression intensities of programmed death-ligand 1 (PD-L1), CD4, CD8, CD20, FoxP3, and CK in whole tumor tissues were evaluated. The enrolled patients showed general characteristics, mostly FIGO stage III/IV and responsive to chemotherapy. Each immune marker showed diverse positive densities, and each tumor sample represented its immune characteristics as an inflamed tumor or noninflamed tumor. No marker was associated with survival as a single one. Interestingly, high ratios of CD8 to FoxP3 and CD8 to PD-L1 were related to the favorable overall survival (77 vs. 39 months, 84 vs. 47 months, respectively), and CD8 to PD-L1 ratio was also a significant prognostic factor (HR 0.621, 95% CI 0.420-0.917,

Indexed as

AdultAgedB7-H1 AntigenBiomarkers, TumorCD8 AntigensCystadenocarcinoma, SerousFemaleFluorescent Antibody TechniqueForkhead Transcription FactorsHumansMiddle AgedMultivariate AnalysisNeoplasm GradingOvarian NeoplasmsPrognosisStaining and LabelingB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD8 AntigensForkhead Transcription FactorsFOXP3 protein, humanCD8FoxP3immunoprofilingmultiplex IHCovarian cancerPD-L1quantitative analysis

Identifiers

PMID34502561
PMCPMC8431807
OpenAlexW3196865002

What OpenQuestion holds

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LicenceCC BY
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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.