Evidence map›Paper›PMID 27045589›Full record

ArticlePloS one2016

Co-Targeting of JNK and HUNK in Resistant HER2-Positive Breast Cancer.

Kendall Phelps-Polirer, Melissa A Abt, Danzell Smith, Elizabeth S Yeh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Biomedicines · 2022
    Review
  6. Article
  7. Selective inhibitors for JNK signalling: a potential targeted therapy in cancer.Journal of enzyme inhibition and medicinal chemistry · 2020
    Review
  8. Article
  9. Article
  10. HUNK Phosphorylates Rubicon to Support Autophagy.International journal of molecular sciences · 2019
    Article
  11. Article
  12. Protective role of JNK inhibitor SP600125 in sepsis-induced acute lung injury.International journal of clinical and experimental pathology · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. 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

4 authors at 2 institutions in 1 country.

Kendall Phelps-PolirerDepartment of Health Sciences, Clemson University, Columbia, SC, United States of America.
Melissa A AbtDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, SC, United States of America.
Danzell SmithDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, United States of America.
Elizabeth S YehDepartment of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, SC, United States of America.
Medical University of South Carolina · USClemson University · US

Funding

MUSC Minority Student Development ProgramR25GM072643 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ERGUL, ADVIYE, RINKER, JENNIFER ANNE · 2005 to 2023
$5.8M
Overcoming Resistance in HER2-positive Breast CancerR01CA187305 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YEH, ELIZABETH S · 2015 to 2019
$1.8M
NCI NIH HHS R01 CA187305NCI NIH HHS R01-CA187305-01A1NIGMS NIH HHS GM072643NIGMS NIH HHS R25 GM072643
6 · The paper itself

Abstract

Strategies for successful primary treatment of HER2-positive breast cancer include use of the HER2 inhibitors trastuzumab or lapatinib in combination with standard chemotherapy. While successful, many patients develop resistance to these HER2 inhibitors indicating an unmet need. Consequently, current research efforts are geared toward understanding mechanisms of resistance and the signaling modalities that regulate these mechanisms. We have undertaken a study to examine whether signaling molecules downstream of epidermal growth factor receptor, which often act as compensatory signaling outlets to circumvent HER2 inhibition, can be co-targeted to overcome resistance. We identified JNK signaling as a potential area of intervention and now show that inhibiting JNK using the pan-JNK inhibitor, SP600125, is effective in the HER2-positive, resistant JIMT-1 xenograft mammary tumor model. We also investigate potential combination strategies to bolster the effects of JNK inhibition and find that co-targeting of JNK and the protein kinase HUNK can prohibit tumor growth of resistant HER2-positive mammary tumors in vivo.

Indexed as

Genes, erbB-2Antineoplastic AgentsAutophagyBreast NeoplasmsCell Line, TumorDrug Resistance, NeoplasmFemaleHumansLapatinibMAP Kinase Kinase 4Protein Kinase InhibitorsProtein Serine-Threonine KinasesQuinazolinesAntineoplastic AgentsHUNK protein, humanLapatinibMAP Kinase Kinase 4Protein Kinase InhibitorsProtein Serine-Threonine KinasesQuinazolines

Identifiers

PMID27045589
PMCPMC4821489
OpenAlexW2331871685

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.