Evidence map›Paper›PMID 37029300›Full record

ArticleOncogene2023

Phase separation of DDX21 promotes colorectal cancer metastasis via MCM5-dependent EMT pathway.

Huabin Gao, Huiting Wei, Yang Yang, Hui Li, Jiangtao Liang, Jiecheng Ye, Fenfen Zhang, Liyuan Wang, Huijuan Shi, Jia Wang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. EMT and cancer stem cells: Drivers of therapy resistance and promising therapeutic targets.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2025
    Review
  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

11 authors at 2 institutions in 1 country.

Huabin Gao *Department of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Huiting Wei *Department of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Yang Yang *Department of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Hui LiDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Jiangtao LiangDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Jiecheng YeDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Fenfen ZhangDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Liyuan WangDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China.
Huijuan ShiDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China. shihj@mail.sysu.edu.cn.
Jia WangGMU-GIBH Joint School of Life Sciences, The Guangdong-Hong Kong-Macau Joint Laboratory for Cell Fate Regulation and Diseases, Guangzhou Medical University, Guangzhou, 511436, China. 2021991028@gzhmu.edu.cn.
Anjia HanDepartment of Pathology, the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510080, China. hananjia@mail.sysu.edu.cn.ORCID 0000-0003-2245-1972
Sun Yat-sen University · CNGuangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA binding proteins (RBPs) contributes to cancer progression, but the underlying mechanism reminds unclear. Here, we find that DDX21, a representative RBP, is highly expressed in colorectal cancer (CRC), which leads to CRC cell migration and invasion in vitro, and CRC to liver metastasis and lung metastasis in vivo. This effect of DDX21 on CRC metastasis is correlated to the activation of Epithelial-mesenchymal transition (EMT) pathway. Moreover, we reveal that DDX21 protein is phase separated in vitro and in CRC cells, which controls CRC metastasis. Phase-separated DDX21 highly binds on MCM5 gene locus, which is markedly reduced when phase separation is disrupted by mutations on its intrinsically disordered region (IDR). The impaired metastatic ability of CRC upon DDX21 loss is restored by ectopic expression of MCM5, indicating MCM5 is a key downstream target of DDX21 for CRC metastasis. Furthermore, co-higher expressions of DDX21 and MCM5 is significantly correlated with poor survival outcomes of stage III and IV CRC patients, indicating the importance of this mechanism in CRC late and metastatic stage. Altogether, our results elucidate a new model of DDX21 in regulating CRC metastasis via phase separation.

Indexed as

Colorectal NeoplasmsEpithelial-Mesenchymal TransitionCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationDEAD-box RNA HelicasesGene Expression Regulation, NeoplasticHumansNeoplasm MetastasisProteinsCell Cycle ProteinsDDX21 protein, humanDEAD-box RNA HelicasesMCM5 protein, humanProteins

Identifiers

PMID37029300
PMCPMC10202810
OpenAlexW4362704966

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.