Evidence map›Paper›PMID 32380476›Full record

ArticleAging2020

Long non-coding RNA CCAT1 promotes colorectal cancer progression by regulating miR-181a-5p expression.

Anquan Shang, Weiwei Wang, Chenzheng Gu, Wei Chen, Wenying Lu, Zujun Sun, Dong Li

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. 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
3.0field-weighted citation impact, top 7% 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. Long Noncoding RNAs as Blood-Based Biomarkers of Diabetic Retinopathy.Translational vision science & technology · 2026
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  6. Expert opinion on therapeutic targets · 2024
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  9. Article
  10. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Role of miR‑181a‑5p in cancer (Review).International journal of oncology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  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 4 institutions in 1 country.

Anquan ShangDepartment of Laboratory Medicine, Tongji Hospital of Tongji University School of Medicine, Shanghai, 200065, China.
Weiwei WangDepartment of Pathology, The Sixth People's Hospital of Yancheng, Yancheng 224001, Jiangsu, China.
Chenzheng GuDepartment of Laboratory Medicine, Tongji Hospital of Tongji University School of Medicine, Shanghai, 200065, China.
Wei ChenDepartment of Pathology, The Sixth People's Hospital of Yancheng, Yancheng 224001, Jiangsu, China.
Wenying LuDepartment of Pathology, The Sixth People's Hospital of Yancheng, Yancheng 224001, Jiangsu, China.
Zujun SunDepartment of Laboratory Medicine, Tongji Hospital of Tongji University School of Medicine, Shanghai, 200065, China.
Dong LiDepartment of Laboratory Medicine, Tongji Hospital of Tongji University School of Medicine, Shanghai, 200065, China.
Tongji Hospital · CNTongji University · CNYancheng Third People's Hospital · CNYancheng Second People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vital roles of long noncoding RNAs (lncRNAs) have been implicated in growing number of studies in tumor development. LncRNA CCAT1 has been recognized as associated with tumor development, yet its relation with colorectal cancer (CRC) remains elusive. Our study aimed at elucidating the function and mechanisms of long non-coding RNA CCAT1 in CRC. From a lncRNA profile dataset of 38 pairs of matched tumor-control colon tissues from colorectal patients housed in The Cancer Genome Atlas (TCGA), we detected 10 upregulated and 10 down-regulated lncRNAs in CRC. Fifty cases of CRC patients were enrolled to analyze the correlation between the expression of CCAT1 and clinical pathology. The inverse correlation of expression and target relationship between CCAT1 and miR-181a-5p were verified using qRT-PCR and dual-luciferase reporter gene assay. Cell viability, colony formation ability, aggression and apoptosis were determined by MTT assay, colony formation assay, Transwell and wound healing assays and flow cytometry analysis. Furthermore, Xenograft model was used to show that knockdown of CCAT1 inhibits tumor growth in vivo. The expression of lncRNA CCAT1 was significantly upregulated in CRC tissues. The CCAT1 expression was positively associated with cancer stage (American Joint Committee on Cancer stage,

Indexed as

Gene Expression Regulation, NeoplasticApoptosisCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease ProgressionHumansRNA, Long NoncodingRNA, NeoplasmCCAT1 long noncoding RNA, humanRNA, Long NoncodingRNA, Neoplasmapoptosiscolorectal cancerlncRNA CCAT1miR-181a-5pproliferation

Identifiers

PMID32380476
PMCPMC7244037
OpenAlexW3022440317

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.