Evidence map›Paper›PMID 34306609›Full record

ArticleJournal of thyroid research2021

Immunohistochemical Analysis of Toll-Like Receptors, MyD88, and TRIF in Human Papillary Thyroid Carcinoma and Anaplastic Thyroid Carcinoma.

Yasuhiro Nihon-Yanagi, Megumi Wakayama, Naobumi Tochigi, Fumi Saito, Hideaki Ogata, Kazutoshi Shibuya

Open access · hybridAbstract read
In one paragraph

Article in Journal of thyroid research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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.

Yasuhiro Nihon-YanagiDepartment of Surgical Pathology, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0001-9663-9367
Megumi WakayamaDepartment of Surgical Pathology, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0001-5506-0586
Naobumi TochigiDepartment of Surgical Pathology, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0003-2538-0380
Fumi SaitoDivision of Breast and Endocrine Surgery, Department of Surgery, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0002-7218-510X
Hideaki OgataDivision of Breast and Endocrine Surgery, Department of Surgery, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0002-3282-0586
Kazutoshi ShibuyaDepartment of Surgical Pathology, Toho University, Omori Hospital, 6-11-1 Omori Nishi, Ota-Ku, Tokyo 143-8541, Japan.ORCID https://orcid.org/0000-0003-3197-488X
Toho University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe hypothesized that innate immune response pathways might be involved in thyroid carcinogenesis. To investigate this hypothesis, we aimed at analyzing the expression of several receptors and molecules in the innate immune system in papillary thyroid carcinoma (PTC) and anaplastic thyroid carcinoma (ATC) tissues.

methodsOf the surgically resected specimens, 11 ATC tissues, 25 PTC tissues, and 8 nodular hyperplasia (NH) tissues were selected and examined for the expression of toll-like receptor (TLR) 2, TLR3, TLR4, TLR5, TLR7, TLR9, the myeloid differentiation primary response gene 88 (MyD88), and toll-interleukin-1 receptor domain-containing adaptor inducing INF-

resultsSeveral TLRs were expressed in each tissue. TLR3 was strongly expressed in all tissues. In contrast, TLR4 was not detected in any tissues. While TLR5 was moderately expressed in NH but significantly reduced in PTC and ATC, TLR9 was absent in NH tissue but moderately expressed in both PTC and ATC. On MyD88 expression, no significant difference was found between PTC and ATC. TRIF was significantly upregulated in PTC and ATC compared to NH. Surprisingly, PTC and ATC tissues exhibited similar expression patterns of TLRs, MyD88, and TRIF.

conclusionThese data suggest the involvement of the innate immune system in both PTC and ATC. Specifically, TLR3-mediated TRIF activation was confirmed in PTC and ATC. This provides new insight into thyroid carcinogenesis.

Identifiers

PMID34306609
PMCPMC8270699
OpenAlexW3176690881

What OpenQuestion holds

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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.