Evidence map›Paper›PMID 34155345›Full record

ArticleOncogene2021

OGT regulated O-GlcNAcylation promotes papillary thyroid cancer malignancy via activating YAP.

Xiaoyan Li, Zhengming Wu, Jing He, Yiting Jin, Chengyu Chu, Yun Cao, Fei Gu, Hongying Wang, Chenjian Hou, Xiuping Liu and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 67 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

11 authors at 3 institutions in 2 countries.

Xiaoyan Li *Department of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.ORCID http://orcid.org/0000-0002-1243-3845
Zhengming Wu *Department of Pharmacology and Moores Cancer Center, University of California San Diego, La Jolla, CA, 92093, USA.
Jing HeDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Yiting JinDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Chengyu ChuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Yun CaoDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Fei GuDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Hongying WangDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Chenjian HouDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Xiuping LiuDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China. xpliu1228@fudan.edu.cn.ORCID http://orcid.org/0000-0003-1935-950X
Qiang ZouDepartment of General Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, China. zouqiang_hs@163.com.ORCID http://orcid.org/0000-0001-9109-9365
Fudan University · CNShanghai Medical College of Fudan University · CNUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of thyroid cancer is growing rapidly during the past decades worldwide. Although most thyroid tumors are curable, some patients diagnosed with distant metastases are associated with poor prognosis. The molecular mechanisms underlying these cases are still largely unknown. Here we found that the upregulated O-Linked N-Acetylglucosamine Transferase (OGT) expression and O-GlcNAcylation (O-GlcNAc) modification in papillary thyroid cancer (PTC) were essential in tumor growth and metastasis. Mass spectrometry analysis showed that YAP was the effector protein modified by OGT. In details, YAP Ser109 O-GlcNAcylation promoted the malignant phenotypes in PTC cells by inducing YAP Ser127 dephosphorylation and activation. Our work clearly showed the critical role of OGT and YAP played in PTC tumors and made it possible for us to seek the clinical potential of manipulating OGT/YAP activity in PTC targeted therapies. These findings also confirmed OGT worked in collaboration with classical Hippo pathway kinases as an upstream regulator of YAP in PTC tumors.

Indexed as

AdultAgedBiomarkersCell Cycle ProteinsDisease SusceptibilityFemaleGlycosylationHumansMaleMiddle AgedN-AcetylglucosaminyltransferasesNeoplasm GradingNeoplasm StagingPolysaccharidesPrognosisThyroid Cancer, PapillaryBiomarkersCell Cycle ProteinsN-AcetylglucosaminyltransferasesOGT protein, humanPolysaccharidesTranscription FactorsYY1AP1 protein, human

Identifiers

PMID34155345
OpenAlexW3175762170

What OpenQuestion holds

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Read underepoch 390

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.