Evidence map›Paper›PMID 34592939›Full record

ArticleBMC cancer2021

LncRNA MCF2L-AS1 aggravates the malignant development of colorectal cancer via targeting miR-105-5p/RAB22A axis.

Wencheng Kong, Hui Li, Lesi Xie, Guangxing Cui, Weigang Gu, Hongchen Zhang, Wencong Ma, Yifeng Zhou

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 15 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

8 authors at 1 institution in 1 country.

Wencheng Kong *Department of Gastrointestinal Surgery, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, Zhejiang, China.
Hui Li *Department of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China.
Lesi XieDepartment of Pathology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, Zhejiang, China.
Guangxing CuiDepartment of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China.
Weigang GuDepartment of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China.
Hongchen ZhangDepartment of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China.
Wencong MaDepartment of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China.
Yifeng ZhouDepartment of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, No. 261 Huanshan Road, Hangzhou, 310006, Zhejiang, China. 17415360@qq.com.ORCID http://orcid.org/0000-0003-3665-907X
Hangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) represents one of the major malignant cancers in the world. It has been demonstrated that long non-coding RNAs (lncRNAs) can cause great influences on various human cancers. Though MCF.2 cell line derived transforming sequence like antisense RNA 1 (MCF2L-AS1) and its carcinogenic effect in CRC has been elucidated by several previous researches, the underlying mechanism remains unknown.

aimWe aimed at exploring the function and regulatory mechanism of MCF2L-AS1 in CRC.

methodsMCF2L-AS1 expression in CRC cells was tested via RT-qPCR assay. The effects of MCF2L-AS1 on the biological properties of CRC cells were testified through functional experiments. The molecular mechanism of MCF2L-AS1 was verified through mechanism experiments.

resultsMCF2L-AS1 was highly expressed in CRC cells, and it could enhance the proliferation, migration, invasion and epithelial-mesenchymal transition (EMT) process of CRC cells. MiR-105-5p was sponged by MCF2L-AS1 in CRC cells and Ras-related protein Rab-22A (RAB22A) was verified to be the downstream target of miR-105-5p. It was verified through rescue assays that RAB22A overexpression or miR-105-5p silencing could reverse the repressive impact of MCF2L-AS1 silencing on CRC progression.

conclusionMCF2L-AS1 accelerated the malignant development of CRC cells by targeting the miR-105-5p/RAB22A axis.

Indexed as

ApoptosisCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease ProgressionEpithelial-Mesenchymal TransitionGene SilencingHumansMicroRNAsNeoplasm InvasivenessNeoplasm Proteinsrab GTP-Binding ProteinsRho Guanine Nucleotide Exchange FactorsMCF2L protein, humanMicroRNAsMIRN105 microRNA, humanNeoplasm ProteinsRAB22A protein, humanrab GTP-Binding ProteinsRho Guanine Nucleotide Exchange FactorsColorectal cancerMCF2L-AS1miR-105-5pRAB22A

Identifiers

PMID34592939
PMCPMC8482615
OpenAlexW3203602911

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.