Evidence map›Paper›PMID 23226615›Full record

ArticleAmerican journal of cancer research2012

The role of the c-Jun N-terminal Kinase signaling pathway in skin cancer.

Jennifer Y Zhang, Maria Angelica Selim

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
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  7. Article
  8. JNK signaling as a target for anticancer therapy.Pharmacological reports : PR · 2021
    Review
  9. Article
  10. Selective inhibitors for JNK signalling: a potential targeted therapy in cancer.Journal of enzyme inhibition and medicinal chemistry · 2020
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Protective role of JNK inhibitor SP600125 in sepsis-induced acute lung injury.International journal of clinical and experimental pathology · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Jennifer Y ZhangDepartment of Dermatology and Pathology, Duke University Durham, NC, USA.
Maria Angelica Selim
Duke University · US

Funding

JUN PROTEINS IN EPIDERMAL HOMEOSTASIS AND NEOPLASIAR01AR057746 · NIAMS · DUKE UNIVERSITY · PI ZHANG, JENNIFER YUNYAN · 2010 to 2014
$1.7M
NIAMS NIH HHS R01 AR057746
6 · The paper itself

Abstract

The c-Jun N-terminal Kinases (JNK), along with Erk and p38, constitute the principle members of the mitogen-activated protein kinase (MAPK) family. JNK functions primarily through AP1 family transcription factors to regulate a plethora of cellular processes, including cell proliferation, differentiation, survival and migration. It also cross-talks and integrates with other signaling pathways in a cell context-specific and cell type-specific manner. The current views of JNK function in various skin cancers and the need of developing JNK subunit-specific inhibitors for cancer type-specific applications have been summarized in this review.

Indexed as

basal cell carcinomacylindromaJNKskin cancersquamous cell carcinoma

Identifiers

PMID23226615
PMCPMC3512184
OpenAlexW74340245

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.