Evidence map›Paper›PMID 39459035›Full record

ReviewPharmaceuticals (Basel, Switzerland)2024

The Impact of Pdcd4, a Translation Inhibitor, on Drug Resistance.

Qing Wang, Hsin-Sheng Yang

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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.

Qing WangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.
Hsin-Sheng YangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-0566-3036

Funding

Targeting the Plk1/Pdcd4/mTORC2 Signaling to Treat Castration-Resistant Prostate CancerR01CA272483 · NCI · UNIVERSITY OF KENTUCKY · PI XIAOQI LIU, Hsin-Sheng Yang · 2023 to 2026
$2.5M
Pdcd4-Rictor Interaction in Suppression of Lung TumorigenesisR01CA279455 · NCI · UNIVERSITY OF KENTUCKY · PI Hsin-Sheng Yang · 2023 to 2026
$2.1M
NIH HHS 1R01CA272483-01A1NIH HHS 1R01CA279455-01A1
6 · The paper itself

Abstract

Programmed cell death 4 (Pdcd4) is a tumor suppressor, which has been demonstrated to efficiently suppress tumorigenesis. Biochemically, Pdcd4 binds with translation initiation factor 4A and represses protein translation. Beyond its role in tumor suppression, growing evidence suggests that Pdcd4 enhances the chemosensitivity of several anticancer drugs. To date, numerous translational targets of Pdcd4 have been identified. These targets govern important signal transduction pathways, and their attenuation may improve chemosensitivity or overcome drug resistance. This review will discuss the signal transduction pathways regulated by Pdcd4 and the potential mechanisms through which Pdcd4 enhances chemosensitivity or counteracts drug resistance.

Indexed as

doxorubicineIF4AfluorouracilIGF1R/IR inhibitorJNK pathwaymTORC2–Akt pathwaypaclitaxelplatinum-containing drugβ-catenin pathway

Identifiers

PMID39459035
PMCPMC11510623

What OpenQuestion holds

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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.