Evidence map›Paper›PMID 28300833›Full record

ArticleCell death & disease2017

PI3K/AKT-mediated upregulation of WDR5 promotes colorectal cancer metastasis by directly targeting ZNF407.

Xin Tan, Shuai Chen, Jiangxue Wu, Jiaxin Lin, Changchuan Pan, Xiaofang Ying, Zhizhong Pan, Lin Qiu, Ranyi Liu, Rong Geng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

11 authors at 5 institutions in 1 country.

Xin TanState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Shuai ChenState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Jiangxue WuState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Jiaxin LinGuangdong Lung Cancer Institute, Guangdong General Hospital & Guangdong Academy of Medical Sciences, Guangzhou 510080, PR China.
Changchuan PanMedical Oncology, Sichuan Cancer Hospital and Institute, Second People's Hospital of Sichuan Province, Chengdu 614000, PR China.
Xiaofang YingDepartment of Radiation Oncology, Hubei Cancer Hospital, Wuhan 430079, PR China.
Zhizhong PanState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Lin QiuState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Ranyi LiuState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Rong GengState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
Wenlin HuangState Key Laboratory of Oncology in South China, Guangzhou 510060, PR China.
State Key Laboratory of Oncology in South ChinaGuangdong Academy of Medical Sciences · CNHubei Cancer Hospital · CNSichuan Cancer Hospital · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the third most common cause of cancer deaths, and has a high rate of liver and lung metastasis. Unfortunately, distant metastasis is the main barrier for advanced CRC therapy and leads to a very low survival rate. In this study, we identified WDR5, a vital factor that regulates vertebrate development and cell self-renewal and reprogramming, as a novel prognostic marker and therapeutic target for CRC patients. We demonstrate that WDR5 is upregulated in CRC tissues and promotes CRC metastasis both in vitro and in vivo. In an effort to investigate the impact of WDR5 on CRC cell fate, we treated CRC cells with growth factor and inhibitor. We report that WDR5 is a novel factor in the metastasis of CRC by triggering epithelial-mesenchymal transition (EMT) process in response to the PI3K/AKT signaling pathway. Moreover, WDR5 shows a direct binding to the ZNF407 promoter on regulating cellular EMT process, leading to CRC metastasis. Hence, our findings strongly position WDR5 as a valuable marker for CRC, and inhibiting WDR5 or the associated signaling pathways may be an effective strategy for the future development of anti-CRC therapy.

Indexed as

Biomarkers, TumorCell LineCell Line, TumorCell MovementColorectal NeoplasmsDNA-Binding ProteinsEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHCT116 CellsHEK293 CellsHistone-Lysine N-MethyltransferaseHT29 CellsHumansIntracellular Signaling Peptides and ProteinsNeoplasm MetastasisPhosphatidylinositol 3-KinasesBiomarkers, TumorDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseIntracellular Signaling Peptides and ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTranscription FactorsWDR5 protein, humanZNF407 protein, human

Identifiers

PMID28300833
PMCPMC5386518
OpenAlexW2595529112

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.