Evidence map›Paper›PMID 29228867›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Long non-coding RNA CCAT1 promotes multiple myeloma progression by acting as a molecular sponge of miR-181a-5p to modulate HOXA1 expression.

Li Chen, Ning Hu, Chao Wang, Hongmian Zhao, Yueli Gu

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.6field-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

52 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Review
  3. Role of miR‑181a‑5p in cancer (Review).International journal of oncology · 2023
    Review
  4. Long non‑coding RNAs in multiple myeloma (Review).International journal of oncology · 2023
    Review
  5. LncRNAArchives of endocrinology and metabolism · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Decoding LncRNAs.Cancers · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Li Chena Department of Hematology , Huaihe Hospital of Henan University , Kaifeng 475000 , Henan China.
Ning Hua Department of Hematology , Huaihe Hospital of Henan University , Kaifeng 475000 , Henan China.
Chao Wanga Department of Hematology , Huaihe Hospital of Henan University , Kaifeng 475000 , Henan China.
Hongmian Zhaoa Department of Hematology , Huaihe Hospital of Henan University , Kaifeng 475000 , Henan China.
Yueli Gub Department of Hematology , The First People's Hospital of Shangqiu , Shangqiu 476100 , Henan China.
Henan University Huaihe Hospital and Huaihe Clinical Institute · CNShangqiu First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is the second most common hematological cancer all over the world. Long non-coding RNA (lncRNA) colon cancer associated transcript-1 (CCAT1) has been reported to play important roles in the development and progression of multiple human malignancies. However, little is known about its functional role and molecular mechanism in MM. The aim of this study was to investigate the clinical and biological significance of CCAT1 in MM. Our data showed that the relative expression levels of CCAT1 were significantly upregulated in MM tissues and cell lines compared with healthy donors and normal plasma cells (nPCs). High expression of CCAT1 was correlated shorter overall survival of MM patients. CCAT1 knockdown significantly inhibited cell proliferation, induced cell cycle arrest at G0/G1 phase and promoted cell apoptosis in vitro, and suppressed tumor growth in vivo. MiR-181a-5p was a direct target of CCAT1, and repression of miR-181a-5p could rescue the inhibition of CCAT1 knockdown on MM progression. In addition, CCAT1 positively regulated HOXA1 expression through sponging miR-181a-5p in MM cells.taken together, lncRNA CCAT1 exerted an oncogenic role in MM by acting as a ceRNA of miR-181a-5p. These results suggest that CCAT1 may serve as a novel diagnostic marker and therapeutic target for MM.

Indexed as

Disease ProgressionAnimalsApoptosisBase SequenceCarcinogenesisCell Cycle CheckpointsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHomeobox A1 ProteinHomeodomain ProteinsHumansMice, Inbred BALB CMice, NudeMicroRNAsCCAT1 long noncoding RNA, humanHomeobox A1 ProteinHomeodomain ProteinsMicroRNAsMIrn181 microRNA, humanRNA, Long NoncodingTranscription FactorsCCAT1HOXA1LncRNAmiR-181a-5pmultiple myeloma

Identifiers

PMID29228867
PMCPMC5914888
OpenAlexW2773093878

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.