Evidence map›Paper›PMID 27983539›Full record

ArticleCancer biomarkers : section A of Disease markers2017

LncRNA-ANCR down-regulation suppresses invasion and migration of colorectal cancer cells by regulating EZH2 expression.

Zhao-Yang Yang, Fang Yang, Ying-Li Zhang, Bao Liu, Meng Wang, Xuan Hong, Yan Yu, Yao-Hui Zhou, Hai Zeng

Erratum issuedAbstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
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  3. Article
  4. Article
  5. Review
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  7. Review
  8. Article
  9. Decoding LncRNAs.Cancers · 2021
    Review
  10. Review
  11. Emerging Roles of LncRNAs in the EZH2-regulated Oncogenic Network.International journal of biological sciences · 2021
    Review
  12. Long Non-coding RNA DANCR in Cancer: Roles, Mechanisms, and Implications.Frontiers in cell and developmental biology · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Zhao-Yang YangDepartment of First Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Fang YangDepartment of First Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Ying-Li ZhangDepartment of Internal Medicine, Harbin Red Cross Central Hospital, Harbin, Heilongjiang, China.
Bao LiuDepartment of First Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Meng WangDepartment of First Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Xuan HongDepartment of First Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Yan YuDepartment of Sixth Internal Medicine, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China.
Yao-Hui ZhouDepartment of Internal Medicine, The First Hospital of Harbin, Harbin, Heilongjiang, China.
Hai ZengDepartment of Internal Medicine, The First Hospital of Harbin, Harbin, Heilongjiang, China.
Harbin Medical University · CNThe First Hospital of Kunming · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our study aimed to explore the effects of long noncoding RNA (lncRNA)-ANCR on the invasion and migration of colorectal cancer (CRC) cells by regulating enhancer of zeste homolog 2 (EZH2) expression. CRC tissues and adjacent normal tissues were collected and CRC SW620 cells line and normal human intestinal epithelial cells (HIECs) were incubated. CRC SW620 cells line was transfected with ANCR-siRNA. The expressions of ANCR and EZH2 mRNA were measured by real-time quantitative polymerase chain reaction (RT-qPCR). EZH2 and trimethylation of H3K27 (H3K27me3) protein expressions were detected using Western blotting. The relationship between ANCR and EZH2 was determined through RNA pull-down and co-immunoprecipitation (co-IP) assays. Cell invasion and migration were determined by Trans-well and cell scratch assays. ANCR, EZH2 and H3K27me3 expressions were up-regulated in CRC tissues and SW620 cells (all P < 0.05). After transfected with ANCR-siRNA, SW620 cells showed decreased ANCR expression and EZH2 mRNA and protein expressions (all P < 0.05). According to the results of RNA pull-down and co-IP assays, ANCR could specifically bind to EZH2. The results of Trans-well and cell scratch tests showed that when ANCR expression was decreased, the invasion and migration abilities of SW620 cells significantly declined (both P < 0.05). In conclusion, these results suggest that lncRNA-ANCR could influence the invasion and migration of CRC cells by specifically binding to EZH2.

Indexed as

Cell Line, TumorCell MovementColorectal NeoplasmsDown-RegulationEnhancer of Zeste Homolog 2 ProteinFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessRNA, Long NoncodingRNA, MessengerANCR long noncoding RNA, humanEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanRNA, Long NoncodingRNA, MessengerANCRcolorectal cancerEZH2invasionLncRNAmigration

Identifiers

PMID27983539
PMCPMC13020607
OpenAlexW2561052169

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.