Evidence map›Paper›PMID 37355885›Full record

ArticleCancer biomarkers : section A of Disease markers2023

An integrative analysis of the tumor suppressors and oncogenes from sexual dimorphism and gene expression alteration features in thyroid cancer.

Yue Huang, Yaoxin Wang, Sining Liu, Zhengmin Xu, Wen-Xia Chen

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
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  4. Prognostic biomarkers based onTranslational cancer research · 2024
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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

5 authors at 2 institutions in 1 country.

Yue HuangDepartment of Otolaryngology-Head and Neck Surgery, Children's Hospital of Fudan University, Shanghai, China.
Yaoxin WangDepartment of Laboratory Medicine, Wu Song Branch, Zhongshan Hospital, Fudan University, Shanghai, China.
Sining LiuDepartment of Otolaryngology-Head and Neck Surgery, Hainan Women and Children's Medical Center, Hainan, China.
Zhengmin XuDepartment of Otolaryngology-Head and Neck Surgery, Children's Hospital of Fudan University, Shanghai, China.
Wen-Xia ChenDepartment of Otolaryngology-Head and Neck Surgery, Children's Hospital of Fudan University, Shanghai, China.
Children's Hospital of Fudan University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of thyroid cancer has risen rapidly over the last decades. Although mortality rates are relatively low compared to other cancers, the rate of new cases started to increase in the early 2000s. While tumor suppressors and oncogenes were recently identified in thyroid cancer, the potential roles of these genes in thyroid cancer remain unclear.

objectiveAnalyze the roles and functions of tumor suppressors and oncogenes in thyroid cancer.

methodsThyroid cancer data were collected from public databases, such as the UCSC Xena database of TCGA thyroid cancer, TISIDB, and UALCAN. The genes frequently associated with unfavorable thyroid cancer were examined and validated. The association of these target genes with thyroid tumorigenesis, stages, subtypes, and survival rates were analyzed. Additionally, the genes aberrantly expressed in thyroid cancer and significantly involved in thyroid tumorigenesis, stages, subtypes, and survival rates were identified.

resultsFemale sex was identified as a risk factor for thyroid cancer. The expression of PAPSS2, PDLIM3, COPZ2, ALDH1B1, ANTXR1, GUF1, and SENP6 negatively correlated with thyroid cancer prognosis.

conclusionFemale sex was a risk factor for thyroid cancer. In addition, our analysis suggested that PAPSS2, PDLIM3, COPZ2, ALDH1B1, ANTXR1, GUF1, and SENP6 are negatively correlated with the prognosis of thyroid cancer. The expression of ANTXR1, GUF1, and PDLIM3 was weakly associated with thyroid cancer's immune and molecular subtypes.

Indexed as

Prostatic HyperplasiaThyroid NeoplasmsCarcinogenesisCysteine EndopeptidasesFemaleGene ExpressionHumansMaleMicrofilament ProteinsOncogenesReceptors, Cell SurfaceSex CharacteristicsANTXR1 protein, humanCysteine EndopeptidasesMicrofilament ProteinsReceptors, Cell SurfaceSENP6 protein, humananticancer drugsDatabaseprognosis genesex differencesthyroid cancer

Identifiers

PMID37355885
PMCPMC12412844
OpenAlexW4381383363

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.