Evidence map›Paper›PMID 29629558›Full record

ArticleMolecules and cells2018

δ-Catenin Increases the Stability of EGFR by Decreasing c-Cbl Interaction and Enhances EGFR/Erk1/2 Signaling in Prostate Cancer.

Nensi Shrestha, Hridaya Shrestha, Taeyong Ryu, Hangun Kim, Shishli Simkhada, Young-Chang Cho, So-Yeon Park, Sayeon Cho, Kwang-Youl Lee, Jae-Hyuk Lee and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecules and cells, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 13 citations in OpenAlex.

  1. Biochemistry · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Delta-Catenin as a Modulator of Rho GTPases in Neurons.Frontiers in cellular neuroscience · 2022
    Review
  8. Article
  9. δ-Catenin Participates in EGF/AKT/p21International journal of molecular sciences · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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 3 institutions in 1 country.

Nensi ShresthaCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Hridaya ShresthaCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Taeyong RyuCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Hangun KimCollege of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Sunchon 57922, Korea.
Shishli SimkhadaCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Young-Chang ChoCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
So-Yeon ParkCollege of Pharmacy and Research Institute of Life and Pharmaceutical Sciences, Sunchon National University, Sunchon 57922, Korea.
Sayeon ChoCollege of Pharmacy, Chung-Ang University, Seoul 06974, Korea.
Kwang-Youl LeeCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Jae-Hyuk LeeChonnam National University Hwasun Hospital & Medical School, Hwasun 58128, Korea.
Kwonseop KimCollege of Pharmacy and Research Institute for Drug Development, Chonnam National University, Gwangju 61186, Korea.
Chonnam National University · KRSunchon National University · KRChung-Ang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

δ-Catenin, a member of the p120-catenin subfamily of armadillo proteins, reportedly increases during the late stage of prostate cancer. Our previous study demonstrates that δ-catenin increases the stability of EGFR in prostate cancer cell lines. However, the molecular mechanism behind δ-catenin-mediated enhanced stability of EGFR was not explored. In this study, we hypothesized that δ-catenin enhances the protein stability of EGFR by inhibiting its lysosomal degradation that is mediated by c-casitas b-lineage lymphoma (c-Cbl), a RING domain E3 ligase. c-Cbl monoubiquitinates EGFR and thus facilitates its internalization, followed by lysosomal degradation. We observed that δ-catenin plays a key role in EGFR stability and downstream signaling. δ-Catenin competes with c-Cbl for EGFR binding, which results in a reduction of binding between c-Cbl and EGFR and thus decreases the ubiquitination of EGFR. This in turn increases the expression of membrane bound EGFR and enhances EGFR/Erk1/2 signaling. Our findings add a new perspective on the role of δ-catenin in enhancing EGFR/Erk1/2 signaling-mediated prostate cancer.

Indexed as

MAP Kinase Signaling SystemCateninsCell Line, TumorDelta CateninErbB ReceptorsGreen Fluorescent ProteinsHumansMaleProstatic NeoplasmsProtein StabilityProto-Oncogene Proteins c-cblRecombinant Fusion ProteinsTransfectionUbiquitinationCateninsCBL protein, humanCTNND1 protein, humanDelta CateninEGFR protein, humanErbB ReceptorsGreen Fluorescent ProteinsProto-Oncogene Proteins c-cblRecombinant Fusion Proteinsc-CblEGFRubiquitinationδ-Catenin

Identifiers

PMID29629558
PMCPMC5935102
OpenAlexW2971861206

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.