Evidence map›Paper›PMID 31332696›Full record

ArticleIn vitro cellular & developmental biology. Animal2019

Long noncoding RNA FGD5-AS1 promotes colorectal cancer cell proliferation, migration, and invasion through upregulating CDCA7 via sponging miR-302e.

Ding Li, Xiaohui Jiang, Xueliang Zhang, Guangxin Cao, Ding Wang, Zhong Chen

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.7field-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

46 citing papers in PubMed, 90 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

6 authors at 1 institution in 1 country.

Ding LiThe First Affiliated Hospital of Soochow University, Medical College of Soochow University, Suzhou, 215006, Jiangsu, China.
Xiaohui JiangDepartment of General Surgery, Affiliated Tumor Hospital of Nantong University, Nantong Tumor Hospital, Nantong, 226361, Jiangsu, China.
Xueliang ZhangDepartment of General Surgery, Affiliated Tumor Hospital of Nantong University, Nantong Tumor Hospital, Nantong, 226361, Jiangsu, China.
Guangxin CaoDepartment of General Surgery, Affiliated Tumor Hospital of Nantong University, Nantong Tumor Hospital, Nantong, 226361, Jiangsu, China.
Ding WangDepartment of General Surgery, Affiliated Tumor Hospital of Nantong University, Nantong Tumor Hospital, Nantong, 226361, Jiangsu, China.
Zhong ChenThe First Affiliated Hospital of Soochow University, Medical College of Soochow University, Suzhou, 215006, Jiangsu, China. chenz9806@sina.com.ORCID http://orcid.org/0000-0002-5155-2038
Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biologic function as well as the mechanism of long noncoding RNAs (lncRNAs) in colorectal cancer (CRC) still remain largely unknown. Long noncoding RNA FGD5 antisense RNA 1 (FGD5-AS1) has been reported to have a promotive effect on other human cancers, but its function in CRC still remains unknown. The expression levels of long noncoding RNA FGD5-AS1, CDCA7 mRNA, and miR-302e were assessed by RT-qPCR. The protein levels of CDCA7 were assessed by Western blot. The function of FGD5-AS1 was detected using cell viability assay, 5-ethynyl-2'-deoxyuridine (EdU) assay, transwell, and caspase-3 activity assay. Additionally, the microRNAs (miRNAs) sponge potential of FGD5-AS1 was examined by RNA immunoprecipitation assay, RNA pull-down assay, and luciferase reporter assay. FGD5-AS1 was increased in colorectal cancer cell lines compared to normal cell lines. Inhibition of FGD5-AS1 suppressed cell proliferation, migration, invasion, and accelerated cell apoptosis in CRC. FGD5-AS1 competitively bound with miR-302e to modulate CDCA7. The inhibiting effects of FGD5-AS1 knockdown on CRC cell proliferation, migration, and invasion, and the promoting effects on CRC cell apoptosis could be revived by miR-302e suppression or CDCA7 upregulation. LncRNA FGD5-AS1 could promote CRC progression through sponging miR-302e and upregulating CDCA7. FGD5-AS1 might serve as a potential therapeutic target for CRC.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBase SequenceBinding, CompetitiveCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsHumansMicroRNAsNeoplasm InvasivenessNuclear ProteinsRNA, Long NoncodingUp-RegulationCDCA7 protein, humanMicroRNAsMIRN302A microRNA, humanNuclear ProteinsRNA, Long NoncodingCDCA7CRCFGD5-AS1miR-302e

Identifiers

PMID31332696
OpenAlexW2964192728

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.