Evidence map›Paper›PMID 32146708›Full record

ArticleHuman cell2020

Long noncoding RNA LINC00520 accelerates the progression of colorectal cancer by serving as a competing endogenous RNA of microRNA-577 to increase HSP27 expression.

Xi-Han Jin, Yong-Gang Hong, Peng Li, Li-Qiang Hao, Ming Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Exosomes promote hFOB1.19 proliferation and differentiation via LINC00520.Journal of orthopaedic surgery and research · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Long Non-Coding RNACancer management and research · 2020
    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

5 authors at 4 institutions in 1 country.

Xi-Han Jin *Department of Colorectal Surgery, Jinhua Municipal Central Hospital, Jinhua, 321000, Zhejiang Province, China.
Yong-Gang Hong *Department of Colorectal Surgery, Changhai Hospital, Second Military Medical University, Shanghai, 200433, China.
Peng LiDepartment of Colorectal Surgery, Jinhua Municipal Central Hospital, Jinhua, 321000, Zhejiang Province, China.
Li-Qiang HaoDepartment of Colorectal Surgery, Changhai Hospital, Second Military Medical University, Shanghai, 200433, China. hao_liqiang@139.com.
Ming ChenDepartment of General Surgery, Taizhou Municipal Hospital, Taizhou, 318000, Zhejiang Province, China. chenming120@hotmail.com.
Jinhua Central Hospital · CNChanghai Hospital · CNSecond Military Medical University · CNTaizhou Municipal Hospital · CN

Funding

the Natural Science Foundation of the Shanghai Science and Technology Commission No. 16ZR1400800
6 · The paper itself

Abstract

The long noncoding RNA (lncRNA) LINC00520 is an important modulator of the oncogenicity of multiple human cancers. However, whether LINC00520 is involved in the malignant characteristics of colorectal cancer (CRC) has not been extensively studied until recently. Therefore, the present study aimed to detect LINC00520 expression in CRC and evaluate its clinical significance in patients with CRC. Functional experiments were conducted to test the biological roles and underlying mechanisms of LINC00520 in CRC progression. In this study, high-LINC00520 expression was verified in CRC tissues and cell lines, and this high expression was associated with patients' unfavorable clinicopathological parameters and shorter overall survival and disease-free survival. Functionally, interference of LINC00520 resulted in a significant decrease of CRC cell proliferation, migration, colony forming ability, and invasion. Mechanistically, LINC00520 functioned as a competing endogenous RNA by sponging microRNA-577 (miR-577) and thereby increasing heat shock protein 27 (HSP27) expression. Rescue experiments revealed that inhibiting miR-577 or restoring HSP27 could abrogate the effects of LINC00520 silencing on malignant phenotypes of CRC. LINC00520 functioned as an oncogenic lncRNA in CRC, and it facilitated CRC progression by regulating the miR-577/HSP27 axis, suggesting that the LINC00520/miR-577/HSP27 axis is an effective target in anticancer management.

Indexed as

Cell Line, TumorCell ProliferationColorectal NeoplasmsDisease ProgressionGene ExpressionHSP27 Heat-Shock ProteinsHumansMicroRNAsMolecular Targeted TherapyRNA, Long NoncodingHSP27 Heat-Shock ProteinsMicroRNAsMIRN577 microRNA, humanRNA, Long NoncodingColorectal cancerHeat shock protein 27LINC00520microRNA-577

Identifiers

PMID32146708
OpenAlexW3009415078

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.