Evidence map›Paper›PMID 33779082›Full record

ArticleYonsei medical journal2021

Clinical Impact of Natural Killer Group 2D Receptor Expression and That of Its Ligand in Ovarian Carcinomas: A Retrospective Study.

Gee Hoon Lee, Hee Jung An, Tae Hoen Kim, Gwangil Kim, Kyung Soon Park, Hyun Park, Tae Ho Lee, Ah Young Kwon

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Gee Hoon LeeDepartment of Biomedical Science, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-0855-1312
Hee Jung AnInstitute for Clinical Research, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-2153-1420
Tae Hoen KimInstitute for Clinical Research, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-2241-6694
Gwangil KimInstitute for Clinical Research, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-4867-9003
Kyung Soon ParkDepartment of Biomedical Science, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-0615-4313
Hyun ParkDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-7825-9165
Tae Ho LeeDepartment of Biomedical Science, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-6797-1042
Ah Young KwonInstitute for Clinical Research, CHA University School of Medicine, Seongnam, Korea.ORCID https://orcid.org/0000-0002-0746-9018
CHA University Bundang Medical Center · KRCHA University · KR

Funding

Korea Health Industry Development Institute HI16C1559
6 · The paper itself

Abstract

purposeNatural killer (NK) cells are innate immune cells with antitumor activity. NKG2D is the most important activating receptor expressed on the NK cell surface; this receptor binds to the ligands MICA/B and ULBPs to activate NK cells. The current study aimed to evaluate the expression of NKG2D by NK cells, and to the evaluate expression of its ligands in ovarian carcinomas; it also examined the clinical relevance of NK receptor/ligand expression by analyzing the relationship between expression, clinicopathological parameters, and prognosis. MATERIALS AND

methodsFormalin-fixed paraffin-embedded archival ovarian high-grade serous carcinoma (HGSC, n=79) tissue samples were used for tissue microarray analysis. The expressions of NK cell markers (CD56 and NKG2D) and NKG2D ligands (MICA/B, ULBP1, ULBP3, and ULBP2/5/6) in carcinoma tissues were evaluated by immunohistochemical staining, and the association between these results and clinical prognostic parameters was analyzed statistically.

resultsULBP1 was highly expressed in 51 cases (64.6%), and ULBP2/5/6 was highly expressed in 56 cases (70.9%) of HGSC. High expression of ULBP1 and ULBP2/5/6 was significantly associated with lower recurrence of HGSC, whereas high expression of ULBP3 was significantly associated with higher recurrence. Multivariate Cox regression analysis revealed that high expression of ULBP1 was associated with increased overall survival and a decreased hazard ratio (0.150,

conclusionHigh expression of ULBP1 predicts a better prognosis for HGSC, suggesting that ULBP1 expression could be a novel prognostic indicator in this subset of carcinomas.

Indexed as

CarcinomaNK Cell Lectin-Like Receptor Subfamily KFemaleGPI-Linked ProteinsHistocompatibility Antigens Class IHumansIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsKiller Cells, NaturalLigandsNeoplasm Recurrence, LocalRetrospective StudiesGPI-Linked ProteinsHistocompatibility Antigens Class IIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsLigandsNK Cell Lectin-Like Receptor Subfamily KNK cellNKG2DNKG2D ligandsovarian carcinomaULBP1

Identifiers

PMID33779082
PMCPMC8007423
OpenAlexW3148396762

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.