Evidence map›Paper›PMID 33325150›Full record

ArticleJournal of cellular and molecular medicine2021

HDAC2 promotes the EMT of colorectal cancer cells and via the modular scaffold function of ENSG00000274093.1.

Zhi-Peng Qi, Ayimukedisi Yalikong, Jia-Wei Zhang, Shi-Lun Cai, Bing Li, Sun Di, Zhen-Tao Lv, En-Pan Xu, Yun-Shi Zhong, Ping-Hong Zhou

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. N-acetyl cysteine through modulation of HDACIBRO neuroscience reports · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Exploring Potential Epigenetic Biomarkers for Colorectal Cancer Metastasis.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Review
  13. HDAC2 as a target for developing anti-cancer drugs.Computational and structural biotechnology journal · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

10 authors.

Zhi-Peng QiEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Ayimukedisi YalikongEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Jia-Wei ZhangDepartment of internal medicine of Xuhui Hospital, Affiliated Zhongshan Hospital, Fudan University, Shanghai, China.
Shi-Lun CaiEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Bing LiEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Sun DiEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Zhen-Tao LvEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
En-Pan XuEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.
Yun-Shi ZhongEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.ORCID 0000-0001-8382-3747
Ping-Hong ZhouEndoscopy Center, Zhongshan Hospital of Fudan University, Shanghai, China.

Funding

China Postdoctoral Science Foundation 2020M681177National Key R&D Program of China 2018YFC1315000/2018YFC1315005National Key R&D Program of China 2019YFC1315800/2019National Natural Science Foundation of China 81672329National Natural Science Foundation of China 82002515Shanghai Sailing Program 20YF1407200
6 · The paper itself

Abstract

Histone deacetylase 2 (HDAC2), a member of the Histone deacetylase family, plays a vital role in various carcinomas. In this study, we identified that HDAC2 expression levels are associated with liver metastasis, higher T stages and poor prognosis in colorectal cancer. HDAC2 down-regulation via lentivirus-mediated expression of HDAC2-targeting shRNA reduced the in vitro migration and invasion ability of HCT116 cell as well as their liver metastasis in nude mouse xenografts. Mechanistically, HDAC2 promotes epithelial-mesenchymal transition (EMT) in colorectal cancer cells by combining HDAC1 with EZH2 (a key histone methyltransferase), possibly through the modular scaffold function of a new lncRNA, ENSG00000274093.1. HDAC2 thus appears to promote CRC cell migration and invasion through binding HDAC1 and EZH2 via ENSG00000274093.1.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsCell MovementColorectal NeoplasmsDown-RegulationFemaleGene Expression Regulation, NeoplasticHCT116 CellsHistone Deacetylase 1Histone Deacetylase 2HumansMaleMiceMice, NudeMiddle AgedNeoplasm InvasivenessHDAC1 protein, humanHistone Deacetylase 1Histone Deacetylase 2RNA, Long Noncodingcolorectal cancerepithelial-mesenchymal transitionhistone deacetylase 2long non-coding RNAs

Identifiers

PMID33325150
PMCPMC7812252

What OpenQuestion holds

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LicenceCC BY
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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.