Evidence map›Paper›PMID 32669362›Full record

ArticleThe Journal of biological chemistry2020

Ubiquitin ligase SMURF2 enhances epidermal growth factor receptor stability and tyrosine-kinase inhibitor resistance.

Paramita Ray, Krishnan Raghunathan, Aarif Ahsan, Uday Sankar Allam, Shirish Shukla, Venkatesha Basrur, Sarah Veatch, Theodore S Lawrence, Mukesh K Nyati, Dipankar Ray

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. 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
–field-weighted citation impact
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.

  1. Review
  2. SMURF2 in Anticancer Therapy: Dual Role in Carcinogenesis and Theranostics.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Advances of E3 ligases in lung cancer.Biochemistry and biophysics reports · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  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

10 authors.

Paramita RayDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Krishnan RaghunathanDepartment of Biophysics, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Aarif AhsanDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Uday Sankar AllamDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Shirish ShuklaDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Venkatesha BasrurDepartment of Pathology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Sarah VeatchDepartment of Biophysics, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Theodore S LawrenceDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Mukesh K NyatiDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA.
Dipankar RayDepartment of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, Michigan, USA dipray@umich.edu.

Funding

Ion channel regulation by heterogeneous membranesR01GM110052 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VEATCH, SARAH L · 2014 to 2022
$2.9M
Integration of EGFR Inhibitors with Radiochemotherapy in Head and Neck CancerR01CA131290 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NYATI, MUKESH K. · 2009 to 2013
$1.5M
Targeting SMURF2 as a novel therapy for EGFR driven tumorsR01CA160981 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAY, DIPANKAR · 2011 to 2015
$1.4M
NCI NIH HHS R01 CA131290NCI NIH HHS R01 CA160981NIGMS NIH HHS R01 GM110052
6 · The paper itself

Abstract

The discovery of activating epidermal growth factor receptor (EGFR) mutations spurred the use of EGFR tyrosine kinase inhibitors (TKIs), such as erlotinib, as the first-line treatment of lung cancers. We previously reported that differential degradation of TKI-sensitive (

Indexed as

Mutation, MissenseAmino Acid SubstitutionAnimalsCHO CellsCricetulusDrug Resistance, NeoplasmEnzyme StabilityErbB ReceptorsErlotinib HydrochlorideHEK293 CellsHumansLung NeoplasmsMCF-7 CellsNeoplasm ProteinsProtein Kinase InhibitorsUbiquitin-Conjugating EnzymesEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideNeoplasm ProteinsProtein Kinase InhibitorsSMURF2 protein, humanUBE2D1 protein, humanUbiquitin-Conjugating EnzymesUbiquitin-Protein LigasesE3 ubiquitin ligaseepidermal growth factor receptor (EGFR)protective ubiquitinationreceptor regulationSmad ubiquitination regulatory factor 2 (SMURF2)tyrosine kinase inhibitor (TKI) resistancetyrosine-protein kinase (tyrosine kinase)ubiquitin-conjugating enzyme H5 (UBCH5)ubiquitylation (ubiquitination)

Identifiers

PMID32669362
PMCPMC7476725

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.