Evidence map›Paper›PMID 33054513›Full record

ArticleCancer biology & therapy2020

Cyclin E overexpression confers resistance to trastuzumab through noncanonical phosphorylation of SMAD3 in HER2+ breast cancer.

Joseph T Decker, Pridvi Kandagatla, Lei Wan, Regan Bernstein, Jeffrey A Ma, Lonnie D Shea, Jacqueline S Jeruss

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Targeting CDK2 to combat drug resistance in cancer therapy.Future oncology (London, England) · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. 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

7 authors at 2 institutions in 1 country.

Joseph T DeckerDepartment of Biomedical Engineering, University of Michigan , Ann Arbor, MI, USA.
Pridvi KandagatlaDepartment of Surgery, Henry Ford Health System , Detroit, MI, USA.
Lei WanDepartment of Surgery, University of Michigan , Ann Arbor, MI, USA.
Regan BernsteinDepartment of Biomedical Engineering, University of Michigan , Ann Arbor, MI, USA.
Jeffrey A MaDepartment of Biomedical Engineering, University of Michigan , Ann Arbor, MI, USA.
Lonnie D SheaDepartment of Biomedical Engineering, University of Michigan , Ann Arbor, MI, USA.
Jacqueline S JerussDepartment of Biomedical Engineering, University of Michigan , Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USHenry Ford Health System · US

Funding

University of Michigan Surgical Oncology Research Training ProgramT32CA009672 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACQUELINE SARA JERUSS, WEIPING ZOU · 1991 to 2026
$6.0M
Measuring Signaling Pathway Dynamics During Tissue Growth in HydrogelsR01CA214384 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2017 to 2021
$1.8M
Chimeric Antigen Receptor T Cell Design Through Living Cell Systems BiologyK01EB028877 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DECKER, JOSEPH THOMAS · 2019 to 2022
$492k
NCI NIH HHS R01 CA214384NCI NIH HHS T32 CA009672NIBIB NIH HHS K01 EB028877
6 · The paper itself

Abstract

The efficacy of trastuzumab, a treatment for HER2+ breast cancer, can be limited by the development of resistance. Cyclin E (CCNE) overexpression has been implicated in trastuzumab resistance. We sought to uncover a potential mechanism for this trastuzumab resistance and focused on a model of CCNE overexpressing HER2+ breast cancer and noncanonical phosphorylation of the TGF-β signaling protein, SMAD3. Network analysis of transcriptional activity in a HER2+, CCNE overexpressing, trastuzumab-resistant cell line (BT474R2) identified decreased SMAD3 activity was associated with treatment resistance. Immunoblotting showed SMAD3 expression was significantly downregulated in BT474R2 cells (

Indexed as

AnimalsBreast NeoplasmsCell ProliferationCyclin EFemaleHumansMiceMice, Inbred NODPhosphorylationSmad3 ProteinTrastuzumabCyclin ESmad3 ProteinSMAD3 protein, humanTrastuzumabbreast cancercyclin EfadraciclibHER2SMAD3Trastuzumab

Identifiers

PMID33054513
PMCPMC7678934
OpenAlexW3093151523

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.