Evidence map›Paper›PMID 32041570›Full record

ArticleBMC cancer2020

Linc01234 promotes cell proliferation and metastasis in oral squamous cell carcinoma via miR-433/PAK4 axis.

Deyu Liu, Xinchun Jian, Pu Xu, Rong Zhu, Yuan Wang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. LncRNA IGFL2-AS1 as a ceRNA Promotes HCT116 Cell Malignant Proliferation via the miR-433-3p/PAK4 Axis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  5. The role of p21-activated kinase 4 in the progression of oral squamous cell carcinoma by targeting PI3K-AKT signaling pathway.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  6. Review
  7. Review
  8. Article
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  10. Article
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Article
  17. Observational
  18. Noncoding RNAs in oral cancer.Wiley interdisciplinary reviews. RNA
    Review
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

5 authors at 1 institution in 1 country.

Deyu LiuDepartment of Oral and Maxillofacial Surgery, Affiliated Haikou Hospital, Xiangya Medical College, Central South University, Haikou, 570208, China.
Xinchun JianDepartment of Oral and Maxillofacial Surgery, Affiliated Haikou Hospital, Xiangya Medical College, Central South University, Haikou, 570208, China. jian_xinchun@163.com.ORCID http://orcid.org/0000-0001-8233-903X
Pu XuDepartment of Oral and Maxillofacial Surgery, Affiliated Haikou Hospital, Xiangya Medical College, Central South University, Haikou, 570208, China. hnxupu@163.com.
Rong ZhuDepartment of Oral and Maxillofacial Surgery, Affiliated Haikou Hospital, Xiangya Medical College, Central South University, Haikou, 570208, China.
Yuan WangCancer Research Institute, Central South University, Changsha, 410008, China.
Central South University · CN

Funding

National Natural Scientific Foundation of China 81260166
6 · The paper itself

Abstract

backgroundIncreasing studies have demonstrated that long non-coding RNAs (lncRNAs) play an important role in tumor progression. However, the potential biological functions and clinical importance of Linc01234 in oral squamous cell carcinoma (OSCC) remain unclear.

methodsWe evaluated the expression profile and prognostic value of Linc01234 in OSCC tissues by RT-qPCR. Then, functional in vitro experiments were performed to investigate the effects of Linc01234 on tumor growth, migration and invasion in OSCC. Mechanistically, RT-qPCR, bioinformatic analysis and dual luciferase reporter assays were performed to identify a competitive endogenous RNA (ceRNA) mechanism involving Linc01234, miR-433-3p and PAK4.

resultsWe found that Linc01234 was clearly upregulated in OSCC tissues and cell lines, and its level was positively associated with T stage, lymph node metastasis, differentiation and poor prognosis of patients with OSCC. Our results shown that Linc01234 inhibited cell proliferation and metastatic abilities in CAL27 and SCC25 cells following its knockdown. Mechanistic analysis indicated that Linc01234 may act as a ceRNA (competing endogenous RNA) of miR-433-3p to relieve the repressive effect of miR-433-3p on its target PAK4.

conclusionsOur results indicated that Linc01234 promotes OSCC progression through the Linc01234/miR-433/PAK4 axis and might be a potential therapeutic target for OSCC.

Indexed as

Gene Expression Regulation, NeoplasticRNA InterferenceRNA, Long Noncoding3' Untranslated RegionsAdultAgedBiomarkers, TumorCarcinoma, Squamous CellCell Line, TumorFemaleGene SilencingHumansMaleMicroRNAsMiddle AgedMouth Neoplasms3' Untranslated RegionsBiomarkers, TumorMicroRNAsMIRN433 microRNA, humanp21-Activated KinasesPAK4 protein, humanRNA, Long NoncodingceRNALinc01234miR-433OSCCPAK4

Identifiers

PMID32041570
PMCPMC7011552
OpenAlexW3012575145

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LicenceCC BY
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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.