Evidence map›Paper›PMID 28423647›Full record

ArticleOncotarget2017

Upregulation of the lncRNA Meg3 induces autophagy to inhibit tumorigenesis and progression of epithelial ovarian carcinoma by regulating activity of ATG3.

Yin-Ling Xiu, Kai-Xuan Sun, Xi Chen, Shuo Chen, Yang Zhao, Qing-Guo Guo, Zhi-Hong Zong

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
  2. Review
  3. Noncoding RNAs: the crucial role of programmed cell death in osteoporosis.Frontiers in cell and developmental biology · 2024
    Review
  4. Review
  5. Role of autophagy and its regulation by noncoding RNAs in ovarian cancer.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
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  15. Review
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  18. Screening and analysis for autophagyZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
    Article
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Yin-Ling XiuDepartment of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110122, China.
Kai-Xuan SunDepartment of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110122, China.
Xi ChenDepartment of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110122, China.
Shuo ChenDepartment of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Yang ZhaoDepartment of Gynecology, The First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Qing-Guo GuoDepartment of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110122, China.
Zhi-Hong ZongDepartment of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110122, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maternally expressed gene 3 (Meg3), a long non-coding RNA, has been reported to be associated with the pathogenesis of multiple malignancies. However, little is known regarding the role of Meg3 in epithelial ovarian cancer (EOC). In this study, we found that the expression of Meg3 was lower in epithelial ovarian carcinoma, and has potential to be considered as a biomarker for ovarian cancer. After transfecting the ovarian cancer cell lines OVCAR3 and A2780 with Meg3, phenotypic changes and autophagy-related molecules were examined. Upregulation of Meg3 inhibited cell proliferation, plate colony formation, induced cell cycle arrest in G2 phases, and promoted apoptosis. Observation of autophagosomes was performed by transmission electron microscopy. The expression levels of LC3-II, ATG3, LAMP1 were elevated, while SQSTM1/p62 expression declined. Upregulated expression of Meg3 also suppressed tumorigenesis in vivo in a xenograft mouse model through upregulating ATG3 expression. RIP (ribonucleoprotein immunoprecipitation) and RNA pull-down assays showed that Meg3 was co-immunoprecipitated with ATG3. In addition, Meg3 protected ATG3 mRNA from degradation following treatment with actinomycin D. Overall, our results suggest that the lncRNA Meg3 acts as a tumor suppressor in EOC by regulating ATG3 activity and inducing autophagy.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisAutophagyAutophagy-Related ProteinsCarcinoma, Ovarian EpithelialCell Cycle CheckpointsCell Line, TumorCell ProliferationCell Transformation, NeoplasticDisease Models, AnimalDisease ProgressionFemaleGenes, Tumor SuppressorHumansMiceATG3 protein, humanAutophagy-Related ProteinsMEG3 non-coding RNA, humanRNA, Long NoncodingUbiquitin-Conjugating Enzymesautophagyepithelial ovarian carcinomalncRNAMeg3tumorigenesis and progression

Identifiers

PMID28423647
PMCPMC5458242
OpenAlexW2592692681

What OpenQuestion holds

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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.