Evidence map›Paper›PMID 33794727›Full record

ArticleCancer biology & therapy2021

LncRNA FGD5-AS1 accelerates cell proliferation in pancreatic cancer by regulating miR-520a-3p/KIAA1522 axis.

Jing Lin, Shasha Liao, Zewa Liu, E Li, Xiaohua Wu, Wanting Zeng

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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  10. Translational lung cancer research · 2025
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  12. Long Non-Coding RNA SNHG3 Promotes the Progression of Cholangiocarcinoma by Regulating the miR-151a-3p/STAT5a Axis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2024
    Article
  13. Article
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  18. Analysis of mJournal of Cancer · 2024
    Article
  19. Effect of tumor exosome-derived Lnc RNA HOTAIR on the growth and metastasis of gastric cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  20. Article
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 4 institutions in 2 countries.

Jing LinDepartment of Oncology, The First Affiliated Hospital of Shantou Univresity Medical College, Shantou, Shantou, Guangdong, China.
Shasha LiaoDepartment of Oncology, Shantou Longhu people's Hospital, Shantou, Guangdong, China.
Zewa LiuDepartment of Oncology, The First Affiliated Hospital of Shantou Univresity Medical College, Shantou, Shantou, Guangdong, China.
E LiDepartment of Oncology, Shantou Longhu people's Hospital, Shantou, Guangdong, China.
Xiaohua WuDepartment of Oncology, Shantou Longhu people's Hospital, Shantou, Guangdong, China.
Wanting ZengUniversity College London, London, UK.
Shantou University · CNYue Bei People's Hospital · CNFirst Affiliated Hospital of Shantou University Medical College · CNUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, FGD5 antisense RNA 1 (FGD5-AS1) was confirmed to be the long non-coding RNAs (lncRNAs) that could accelerate the development of multiple cancers. Nevertheless, specific biological functions and latent mechanism of FGD5-AS1 were not yet clear in pancreatic cancer (PC). This research was aimed to search the functions of FGD5-AS1 on the PC progression. The expression of FGD5-AS1 in PC cells was tested by using RT-qPCR assay. Colony formation assay, EdU assay, flow cytometry assay and transwell assay as well as western blot were adopted to test the cell abilities of proliferation, apoptosis and migration, separately. Furthermore, RIP experiment and pull down assay were applied for validating the correlation FGD5-AS1, miR-520a-3p and KIAA1522. As a result, the abnormal high expression of FGD5-AS1 was observed in PC cells. And cell proliferative and migratory abilities could be restrained via FGD5-AS1 depletion. Moreover, FGD5-AS1 was proven to combine with miR-520a-3p directly. It was also confirmed that KIAA1522 could be targeted by miR-520a-3p. Rescue assay results indicated that overexpressed KIAA1522 could reverse the repressive function of silencing FGD5-AS1 on PC progression. Taken together, FGD5-AS1 accelerated cell proliferation and migration via sponging miR-520a-3p and upregulating KIAA1522.

Indexed as

Cell Line, TumorCell ProliferationHumansIntracellular Signaling Peptides and ProteinsMicroRNAsPancreatic NeoplasmsRNA, Long NoncodingUp-RegulationIntracellular Signaling Peptides and ProteinsKIAA1522 protein, humanMicroRNAsMIRN520 microRNA, humanRNA, Long NoncodingFGD5-AS1kiaa1522miR-520a-3ppancreatic cancer

Identifiers

PMID33794727
PMCPMC8043177
OpenAlexW3145238338

What OpenQuestion holds

Textmetadata
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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.