Evidence map›Paper›PMID 34306175›Full record

ArticleComputational and mathematical methods in medicine2021

miR-30a-5p Regulates Viability, Migration, and Invasion of Lung Adenocarcinoma Cells via Targeting ECT2.

Sangsang Chen, Xuqing Zhu, Jing Zheng, Tingting Xu, Yinmin Xu, Feng Chen

RetractedAbstract readRetracted Publication
In one paragraph

Article in Computational and mathematical methods in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Sangsang ChenDepartment of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310000, China.
Xuqing ZhuDepartment of Gastroenterology, Taizhou Municipal Hospital, Taizhou 318000, China.
Jing ZhengDepartment of Respiratory Medicine, Taizhou Municipal Hospital, Taizhou 318000, China.
Tingting XuDepartment of Respiratory Medicine, Taizhou Municipal Hospital, Taizhou 318000, China.
Yinmin XuDepartment of Respiratory Medicine, Affiliated Hospital of Shaoxing University, Shaoxing 312000, China.
Feng ChenDepartment of Respiratory Medicine, Taizhou Municipal Hospital, Taizhou 318000, China.ORCID https://orcid.org/0000-0003-3835-5280

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe abnormal expression of epithelial cell transforming sequence 2 (ECT2) is often considered the driving factor for the growth and invasion of tumors. This study was performed to investigate the regulatory effect of miR-30a-5p and ECT2 on lung adenocarcinoma (LUAD), which provides a basis for the effective clinical treatment of LUAD.

methodsThe mature miRNAs, expression data of mRNAs, and clinical data of LUAD were downloaded from The Cancer Genome Atlas (TCGA). The expression levels of ECT2 mRNA and miR-30a-5p in cancer cell lines were detected by qRT-PCR. Western blot was performed to test the expression of ECT2 protein. The targeting relationship between miR-30a-5p and ECT2 was verified by dual-luciferase assay. The CCK-8 method and Transwell assay were conducted to test the viability, migratory, and invasive abilities of cells.

resultsECT2 expression was upregulated in LUAD and was significantly correlated with the LUAD clinical stage and pathologic T stage, and the expression of its upstream regulatory gene miR-30a-5p was downregulated. miR-30a-5p targeted ECT2 in LUAD. Downregulation of ECT2 could inhibit the viability, migration, and invasion of LUAD cells, which could be reversed by simultaneously suppressing the expression of miR-30a-5p.

conclusionOur results suggested that miR-30a-5p repressed the malignant progression of LUAD via downregulating ECT2. miR-30a-5p and ECT2 may be effective targets for LUAD patients.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorCell Line, TumorCell MovementCell SurvivalComputational BiologyDown-RegulationGene Expression Regulation, NeoplasticHumansLung NeoplasmsMicroRNAsMolecular Targeted TherapyNeoplasm InvasivenessProto-Oncogene ProteinsRNA, MessengerUp-RegulationBiomarkers, TumorECT2 protein, humanMicroRNAsMIRN30a microRNA, humanProto-Oncogene ProteinsRNA, Messenger

Identifiers

PMID34306175
PMCPMC8279846

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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.