Evidence map›Paper›PMID 32615729›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2020

Mechanisms of the Impact of Hashimoto Thyroiditis on Papillary Thyroid Carcinoma Progression: Relationship with the Tumor Immune Microenvironment.

Oksana Sulaieva, Olena Chernenko, Oleksiy Selesnov, Oleksandr Nechay, Oleksandr Maievskyi, Tetyana Falalyeyeva, Nazarii Kobyliak, Olena Tsyryuk, Yurii Penchuk, Dmytro Shapochka

Open access · diamondAbstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

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  13. Hashimoto's thyroiditis is negatively associated with lymph node metastasis in PTMC.Journal of cancer research and clinical oncology · 2023
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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

10 authors at 4 institutions in 1 country.

Oksana SulaievaLaboratory of Pathology CSD Health Care, Kyiv, Ukraine.
Olena ChernenkoUkrainian Research and Practical Center for Endocrine Surgery, Kyiv, Ukraine.
Oleksiy SelesnovLaboratory of Pathology CSD Health Care, Kyiv, Ukraine.
Oleksandr NechayUkrainian Research and Practical Center for Endocrine Surgery, Kyiv, Ukraine.
Oleksandr MaievskyiInstitute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine.
Tetyana FalalyeyevaInstitute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine.
Nazarii KobyliakDepartment of Endocrinology, Bogomolets National Medical University, Kyiv, Ukraine.
Olena TsyryukInstitute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine.
Yurii PenchukInstitute of Biology and Medicine, Taras Shevchenko National University of Kyiv, Kyiv, Ukraine.
Dmytro ShapochkaLaboratory of Pathology CSD Health Care, Kyiv, Ukraine.
Taras Shevchenko National University of Kyiv · UAKyiv City Clinical Oncology Center · UAResearch Institute of Ukrainian Studies · UABogomolets National Medical University · UA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe relationship between Hashimoto thyroiditis (HT) and papillary thyroid carcinoma (PTC) remains uncertain. We assessed the impact of HT on the tumor immune microenvironment (TIME) in PTC.

methodsThirty patients with PTC (group 1) and 30 patients with PTC and HT (group 2) were enrolled in this pilot study. The distribution and number of CD8+ lymphocytes, plasma cells (CD138+), regulatory T cells (forkhead box P3 [FOXP3+)], mast cell tryptase (MCT+), and M2 macrophages (CD163+) were evaluated. To test the hypothesis that HT impacts PTC development via signal transducer and activator of transcription 6 (STAT6) activation and M2 macrophage polarization, we investigated STAT6 expression in tumor and stromal cells. We also evaluated vascular endothelial growth factor (VEGF) expression by lymph node metastasis (LNM) status.

resultsTIME showed significant between-group differences. Group 1 patients demonstrated immune desert or immune-excluded immunophenotypes, while an inflamed phenotype with more CD8+ cells (P<0.001) predominated in group 2. Immune-excluded TIME was associated with the highest LNM rate. In PTC, LNM was associated with more numerous CD163+ cells. Moreover, LNM in group 1 was associated with increased numbers of mast cells peritumorally and FOXP3+ cells intratumorally and peritumorally. Group 2 demonstrated higher STAT6 but not higher VEGF expression in tumor cells. High VEGF expression was associated with LNM regardless of HT status.

conclusionConcomitant HT impacted PTC signaling via STAT6 and TIME by increasing the number of CD8+ cells. LNM is associated with increases in CD163+ cells and VEGF expression in PTC, whereas HT affected LNM through different mechanisms.

Indexed as

AdultCarcinoma, PapillaryDisease ProgressionFemaleFollow-Up StudiesHashimoto DiseaseHumansMaleMiddle AgedPilot ProjectsPrognosisThyroid NeoplasmsT-Lymphocytes, RegulatoryTumor MicroenvironmentYoung AdultHashimoto diseaseMacrophagesMetastasisThyroid cancer, papillaryT-lymphocytes

Identifiers

PMID32615729
PMCPMC7386119
OpenAlexW3037936416

What Socratic 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 Socratic graph.