Evidence map›Paper›PMID 34181355›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2021

NFATc1 is Suppressed in Tumor Microenvironment of Hodgkin Lymphoma.

Krisna Murti, Neti Neti, Nyiayu Fauziah Kurniawati, Ika Kartika, Riana Sari Puspita Rasyid, Zen Hafy

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 1 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

6 authors at 1 institution in 1 country.

Krisna MurtiDepartment of Anatomic Pathology Faculty of Medicine Universitas Sriwijaya, Indonesia.
Neti NetiDepartment of Anatomic Pathology Faculty of Medicine Universitas Sriwijaya, Indonesia.
Nyiayu Fauziah KurniawatiDepartment of Anatomic Pathology Faculty of Medicine Universitas Sriwijaya, Indonesia.
Ika KartikaDepartment of Anatomic Pathology Faculty of Medicine Universitas Sriwijaya, Indonesia.
Riana Sari Puspita RasyidDepartment of Histology Faculty of Medicine Universitas Sriwikaya, Indonesia.
Zen HafyDepartment of Histology Faculty of Medicine Universitas Sriwikaya, Indonesia.
Sriwijaya University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aims of this research are to evaluate the expression and distribution of NFATc1 in tumor microenvironment of Hodgkin lymphoma.

methodsTwenty-eight cases of Hodgkin lymphoma were selected. Clinicopathological data of age, gender, location and subtypes were obtained. Immunohistochemistry was performed to the all cases by using anti-CD163, anti-NFATc1 and anti-PD-L1 antibodies. All protein expression was calculated by using Image J software.

resultsNuclear expression of NFATc1 was not observed in Hodgkin cells neither in TAM nor in small lymphocytes surrounding Hodgkin cells in all the samples, this meant that NFATc1 showed negative nuclear expression in almost all these cells. Cytoplasmic expression of NFATc1 was observed in small lymphocytes surrounding tumor cells. While there were only few small lymphocytes which were located far from tumor cells showed nuclear expression of NFATc1. Meanwhile, 57.14% samples showed high density of TAMs CD163+, and 50% tumor cells as well as 50% TAMs exhibited positive PD-L1 expression. In addition, all macrophages did not have NFATc1 expression both in their nuclei and in their cytoplasm.

conclusionNFATc1 was suppressed both in Hodgkin cells and inflammatory cells surrounding the tumor cells. This condition may contribute to progressivity and aggressiveness of the diseases. Therefore, certain mechanisms to reactivate functional NFATc1 in HL tumor microenvironment may be necessary; hence, the tumor cells are able to be eradicated by patient's immune mechanisms.

Indexed as

Tumor MicroenvironmentAdultAntigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenBiomarkers, TumorCD163 AntigenFemaleHodgkin DiseaseHumansMaleMiddle AgedNFATC Transcription FactorsReceptors, Cell SurfaceAntigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenBiomarkers, TumorCD163 AntigenCD274 protein, humanNFATC1 protein, humanNFATC Transcription FactorsReceptors, Cell SurfaceCD163Hodgkin lymphomaNFATc1PD-L1Tumor Microenvironment

Identifiers

PMID34181355
PMCPMC8418861
OpenAlexW3173556795

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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.