Evidence map›Paper›PMID 33751775›Full record

ArticleMolecular oncology2021

The direct miR-874-3p-target FAM84A promotes tumor development in papillary thyroid cancer.

Yu Ding, Luyao Wu, Xi Zhuang, Jingsheng Cai, Houchao Tong, Yan Si, Hao Zhang, Xiaoting Wang, Meiping Shen

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
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  11. miR-874: An Important Regulator in Human Diseases.Frontiers in cell and developmental biology · 2022
    Review
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

9 authors at 1 institution in 1 country.

Yu DingDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Luyao WuDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Xi ZhuangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Jingsheng CaiDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Houchao TongDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Yan SiDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Hao ZhangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Xiaoting WangDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.
Meiping ShenDepartment of General Surgery, the First Affiliated Hospital of Nanjing Medical University, China.ORCID 0000-0002-6786-0270
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the improvement in diagnostic technology, the incidence of thyroid cancer (TC) is on the rise. Papillary thyroid carcinoma (PTC) is the most common pathological type of thyroid cancer; therefore, it is important to explore some valuable molecular targets to improve the treatment and prognosis of PTC. Studies have shown that family with sequence similarity 84, member A (FAM84A) is involved in the development of various tumors. However, the role of FAM84A in PTC remains unknown. Herein, we explored the biological function and specific molecular mechanism of FAM84A in PTC. Results indicated that FAM84A was upregulated in PTC tissues and cells. In addition, patients with higher FAM84A expression tended to possess larger tumor size, higher lymph node metastasis rate, and advanced TNM stage. Further studies indicated that downregulation of FAM84A could inhibit the development of PTC in vitro and in vivo by repressing the epithelial-mesenchymal transition (EMT) and Wnt/β-catenin signaling pathway. Moreover, FAM84A was confirmed to be negatively regulated by tumor suppressor miR-874-3p. In conclusion, our findings suggest that FAM84A may act as a potential diagnostic and therapeutic target for PTC.

Indexed as

AdultAgedAnimalsCarcinogenesisCase-Control StudiesCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMaleMiceMicroRNAsMiddle AgedLRATD1 protein, humanMicroRNAsMIRN874 microRNA, humanNeoplasm ProteinsFAM84AmiR-874-3ppapillary thyroid carcinomaWnt/β-catenin signaling

Identifiers

PMID33751775
PMCPMC8096794
OpenAlexW3135173891

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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.