Evidence map›Paper›PMID 31397203›Full record

ArticleCell cycle (Georgetown, Tex.)2019

LncRNA MALAT1/miR-181a-5p affects the proliferation and adhesion of myeloma cells via regulation of Hippo-YAP signaling pathway.

Yanbei Sun, Tingxiu Jiang, Yongqing Jia, Jingyun Zou, Xiaoxiao Wang, Weiying Gu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  4. Long non-coding RNAMolecular therapy. Nucleic acids · 2025
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  6. Expert opinion on therapeutic targets · 2024
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  7. Article
  8. Article
  9. Review
  10. Role of miR‑181a‑5p in cancer (Review).International journal of oncology · 2023
    Review
  11. Long non‑coding RNAs in multiple myeloma (Review).International journal of oncology · 2023
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Long Non-Coding RNA MALAT1 Contributed to the Proliferation of PNH Clone in Paroxysmal Nocturnal Hemoglobinuria PatientsTurkish journal of haematology : official journal of Turkish Society of Haematology · 2021
    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

6 authors at 2 institutions in 1 country.

Yanbei SunDepartment of Nephrology, The Third Affiliated Hospital of Soochow University , Changzhou , China.
Tingxiu JiangDepartment of Hematology, Liuzhou Worker's Hospital, The Fourth Affiliated Hospital of Guangxi Medical University , Liuzhou , China.
Yongqing JiaDepartment of Hematology, The Third Affiliated Hospital of Soochow University , Changzhou , China.
Jingyun ZouDepartment of Hematology, The Third Affiliated Hospital of Soochow University , Changzhou , China.
Xiaoxiao WangDepartment of Hematology, The Third Affiliated Hospital of Soochow University , Changzhou , China.
Weiying GuDepartment of Hematology, The Third Affiliated Hospital of Soochow University , Changzhou , China.
Soochow University · CNFourth Affiliated Hospital of Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a plasma cells malignant proliferative disease, especially in aged people. LncRNAs have been considered as important regulators in MM. This research was to study the effect of LncRNA MALAT1 on the proliferation and adhesion of myeloma cells and whether Long non-coding RNAs MALAT1(LncRNA MALAT1) plays its regulative role through Hippo-YAP signaling pathway by targeting miR-181a-5p. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analysis was used to detect the LncRNA MALAT1/miR-181a-5p expression and improve the transfection efficiency. Western blot analysis was used to analyze the expression of proliferation and apoptosis related proteins and Hippo-Yes-associated protein (YAP) signaling pathway related proteins. Cell proliferative ability and cell apoptosis were respectively determined by Cell Counting Kit-8 (CCK-8) assay and flow cytometry analysis. ELISA assay was for the determination of adherence factors. Immunohistochemistry was to detect the expression of proliferation and adhesion related proteins. LncRNA MALAT1 targeting gene was determined by Dual-luciferase reporter assay. LncRNA MALAT1 was increased in MM cells and LncRNA MALAT1 interference could inhibit cell proliferation and promote cell apoptosis with the changes in the related proteins. Also, LncRNA MALAT1 interference could inhibit cell adhesion through Hippo-YAP signaling pathway. MiR-181a-5p was demonstrated to be a target of LncRNA MALAT1 and miR-181a-5p overexpression could also regulate the changes in cellular behavior in accordance with the LncRNA MALAT1 interference. In addition, LncRNA MALAT1 interference could decrease the expression of miR-181a-5p and inhibit the growth of tumor. In conclusion, this study showed that LncRNA MALAT1 interference inhibited the proliferation and adhesion of myeloma cells by the up-regulation of miR-181a-5p through activating the Hippo-YAP signaling pathway.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsApoptosisCell AdhesionCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHippo Signaling PathwayHumansMaleMiceMice, NudeMicroRNAsMultiple MyelomaPhosphorylationProtein Serine-Threonine KinasesAdaptor Proteins, Signal TransducingMicroRNAsMIrn181 microRNA, humanProtein Serine-Threonine KinasesRNA, Long NoncodingRNA, Small InterferingTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsadhesionHippo-YAP signaling pathwayLncRNA MALAT1/miR-181a-5pmyeloma cellsproliferation

Identifiers

PMID31397203
PMCPMC6738907
OpenAlexW2968098695

What OpenQuestion holds

Textmetadata
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.