Evidence map›Paper›PMID 28388267›Full record

ArticleCell cycle (Georgetown, Tex.)2017

Activation of Notch pathway is linked with epithelial-mesenchymal transition in prostate cancer cells.

Lianhua Zhang, Jianjun Sha, Guoliang Yang, Xuyuan Huang, Juanjie Bo, Yiran Huang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
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  8. Article
  9. Study Deciphering the Crucial Involvement of Notch Signaling Pathway in Human Cancers.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Notch signaling, hypoxia, and cancer.Frontiers in oncology · 2023
    Review
  15. Article
  16. Review
  17. Review
  18. Sirtuins and Hypoxia in EMT Control.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  19. Review
  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

6 authors at 2 institutions in 1 country.

Lianhua Zhanga Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Jianjun Shaa Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Guoliang Yanga Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Xuyuan Huanga Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Juanjie Boa Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Yiran Huanga Department of Urology , Renji Hospital, School of Medicine, Shanghai Jiao Tong University , Shanghai , China.
Renji Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notch signaling has been reported to play an essential role in tumorigenesis. Several studies have suggested that Notch receptors could be oncoproteins or tumor suppressors in different types of human cancers. Emerging evidence has suggested that Notch pathway regulates cell growth, apoptosis, cell cycle, and metastasis. In the current study, we explore whether Notch-1 could regulate the cell invasion and migration as well as EMT (epithelial-mesenchymal transition) in prostate cancer cells. We found that overexpression of Notch-1 enhanced cell migration and invasion in PC-3 cells. However, downregulation of Notch-1 retarded cell migration and invasion in prostate cancer cells. Importantly, we observed that overexpression of Notch-1 led to EMT in PC-3 cells. Notably, we found that EMT-type cells are associated with EMT markers change and cancer stem cell phenotype. Taken together, we concluded that downregulation of Notch-1 could be a promising approach for inhibition of invasion in prostate cancer cells, which could be useful for the treatment of metastatic prostate cancer.

Indexed as

Cell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionHumansMaleNeoplasm InvasivenessNeoplasm MetastasisNeoplastic Stem CellsProstatic NeoplasmsReceptor, Notch1Signal TransductionNOTCH1 protein, humanReceptor, Notch1EMTinvasionmigrationNotch-1prostate cancer

Identifiers

PMID28388267
PMCPMC5462088
OpenAlexW2604553543

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.