Evidence map›Paper›PMID 34522455›Full record

ArticleAmerican journal of cancer research2021

bFGF-mediated phosphorylation of δ-catenin increases its protein stability and the ability to induce the nuclear redistribution of β-catenin.

Gen Chen, Ning An, Yu Zhu, Rui Zhou, Myung-Giun Noh, Hangun Kim, Hyoung Jae Lee, Yingjie Shen, Young-Chang Cho, Litai Jin and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Roles and regulation of δ-catenin in tumorigenesis and neuronal diseases.Frontiers in cell and developmental biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

13 authors at 4 institutions in 2 countries.

Gen ChenCollege of Pharmacy, Chonnam National University Gwangju 61186, Korea.
Ning AnDepartment of Pharmacy, Ningbo Medical Center Lihuili Hospital Ningbo 315041, P. R. China.
Yu ZhuSchool of Pharmaceutical Science, Wenzhou Medical University Wenzhou 325000, P. R. China.
Rui ZhouCollege of Pharmacy, Sunchon National University Sunchon 57922, Korea.
Myung-Giun NohDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST) Gwangju 61005, Korea.
Hangun KimCollege of Pharmacy, Sunchon National University Sunchon 57922, Korea.
Hyoung Jae LeeCollege of Pharmacy, Chonnam National University Gwangju 61186, Korea.
Yingjie ShenCollege of Pharmacy, Chonnam National University Gwangju 61186, Korea.
Young-Chang ChoCollege of Pharmacy, Chonnam National University Gwangju 61186, Korea.
Litai JinSchool of Pharmaceutical Science, Wenzhou Medical University Wenzhou 325000, P. R. China.
Weitao CongSchool of Pharmaceutical Science, Wenzhou Medical University Wenzhou 325000, P. R. China.
Jae-Hyuk LeeChonnam National University Hwasun Hospital & Medical School Hwasun 58128, Korea.
Kwonseop KimCollege of Pharmacy, Chonnam National University Gwangju 61186, Korea.
Chonnam National University · KRWenzhou Medical University · CNSunchon National University · KRGwangju Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we have shown that δ-catenin strengthened the epidermal growth factor receptor (EGFR)/Erk1/2 signaling pathway through the association between EGFR and δ-catenin. Now, we further analyzed the correlation between basic fibroblast growth factor (bFGF)/fibroblast growth factor receptor 1 (FGFR1) and δ-catenin in prostate cancer and investigated the molecular mechanism underlying the role of bFGF/FGFR1 modulation in CWR22Rv-1 (Rv-1) cells. Here, we demonstrated that bFGF phosphorylated the tyrosine residues of δ-catenin in Rv-1 cells and further proved that the bFGF mediated FGFR1/δ-catenin tyrosine phosphorylation was time dependent. Furthermore, we demonstrated that bFGF stabilized the expression of δ-catenin through weakening its association with GSK3β and enhancing its stability to induce β-catenin into the nuclear by strengthening the processing of E-cadherin. In a word, these results indicated that bFGF/FGFR1 signaling pathway could enhance the tumor progression of prostate cancer via δ-catenin.

Indexed as

bFGFE-cadherinFGFR1GSK3βδ-catenin

Identifiers

PMID34522455
PMCPMC8414378
OpenAlexW3200417043

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.