Evidence map›Paper›PMID 31094023›Full record

ArticleCell proliferation2019

Non-coding RNA MFI2-AS1 promotes colorectal cancer cell proliferation, migration and invasion through miR-574-5p/MYCBP axis.

Chenglong Li, Fengbo Tan, Qian Pei, Zhongyi Zhou, Yuan Zhou, Lunqiang Zhang, Dan Wang, Haiping Pei

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. miR-574-5p in epigenetic regulation and Toll-like receptor signaling.Cell communication and signaling : CCS · 2024
    Review
  5. Article
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  8. Review
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  10. Review
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  13. Role of Non-Coding RNAs in Colorectal Cancer: Focus on Long Non-Coding RNAs.International journal of molecular sciences · 2022
    Review
  14. Article
  15. CTBP1-AS2 promoted non-small cell lung cancer progression via sponging the miR-623/MMP3 axis.Environmental science and pollution research international · 2022
    Article
  16. Article
  17. Non-coding antisense transcripts: fine regulation of gene expression in cancer.Computational and structural biotechnology journal · 2022
    Review
  18. Article
  19. 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

8 authors at 1 institution in 1 country.

Chenglong LiDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Fengbo TanDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Qian PeiDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Zhongyi ZhouDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Yuan ZhouDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Lunqiang ZhangDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Dan WangDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.
Haiping PeiDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, China.ORCID https://orcid.org/0000-0001-5622-2081
Central South University · CN

Funding

Nature Scientific Foundation of China 81702956The Strategy-Oriented Special Project of Central South University in China ZLXD2017003The XiangYa-Peking University Wei Ming Clinical and Rehabilitation Research Fund xywm2015121
6 · The paper itself

Abstract

objectiveLong non-coding RNAs (lncRNAs) and microRNAs (miRNAs) play essential roles in the tumour progression. LncRNAs mostly act as competing endogenous RNAs (ceRNAs) by sponging miRNAs. This study aimed to study the association of a novel lncRNA MFI2-AS1 with miR-574-5p/MYCBP axis in the development of colorectal cancer (CRC).

methodsNinety-four CRC tissues and paired adjacent non-tumour tissues were included in our study. The relative expression level of MFI2-AS1 was detected, and its relationship with clinico-pathological factors was analysed. Then, the CRC cells lines (LoVo and RKO) were transfected with MFI2-AS1 siRNA, miR-574-5p mimics and inhibitors. Cell proliferation, migration, invasion, cell cycle distribution and DNA damage in response to different transfection conditions were examined. Dual-luciferase reporter assay was performed to identify the target interactions between MFI2-AS1 and miR-574-5p, miR-574-5p and MYCBP.

resultsLncRNA MFI2-AS1 and MYCBP were up-regulated in CRC tissues when compared with adjacent non-tumour tissues. The expression levels of MFI2-AS1 were significantly associated with tumour histological grade, lymph and distant metastasis, TNM stage and vascular invasion. Both MFI2-AS1 siRNA and miR-574-5p mimics inhibited proliferation, migration and invasion in LoVo and RKO cells. The transfection of miR-574-5p inhibitor showed MFI2-AS1 siRNA-induced changes in CRC cells. Dual-luciferase reporter assay revealed target interactions between MFI2-AS1 and miR-574-5p, miR-574-5p and MYCBP.

conclusionsThese findings suggested that lncRNA MFI2-AS1 and MYCBP have promoting effects in CRC tissues. LncRNA MFI2-AS1 promoted CRC cell proliferation, migration and invasion through activating MYCBP and by sponging miR-574-5p.

Indexed as

Cell LineCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDNA-Binding ProteinsGene Expression Regulation, NeoplasticHCT116 CellsHEK293 CellsHT29 CellsHumansMicroRNAsNeoplasm InvasivenessRNA, Long NoncodingRNA, Small InterferingTranscription FactorsDNA-Binding ProteinsMicroRNAsMIRN574 microRNA, humanMYCBP protein, humanRNA, Long NoncodingRNA, Small InterferingTranscription Factorscolorectal cancerLncRNA MFI2-AS1miR-574-5pMYC binding protein

Identifiers

PMID31094023
PMCPMC6668983
OpenAlexW2946369889

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.