Evidence map›Paper›PMID 32316313›Full record

ReviewInternational journal of molecular sciences2020

The p38 MAPK Signaling Activation in Colorectal Cancer upon Therapeutic Treatments.

Angelina Pranteda, Valentina Piastra, Lorenzo Stramucci, Deborah Fratantonio, Gianluca Bossi

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Resistance of E2F4DN to p38Scientific reports · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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  11. The Essential Oil fromPharmaceuticals (Basel, Switzerland) · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Targeting MAPK in Cancer 2.0.International journal of molecular sciences · 2022
    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

5 authors.

Angelina PrantedaOncogenomic and Epigenetic Unit, Department of Diagnostic Research and Technological Innovation, IRCCS-Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144 Rome, Italy.
Valentina PiastraOncogenomic and Epigenetic Unit, Department of Diagnostic Research and Technological Innovation, IRCCS-Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144 Rome, Italy.
Lorenzo StramucciOncogenomic and Epigenetic Unit, Department of Diagnostic Research and Technological Innovation, IRCCS-Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144 Rome, Italy.
Deborah FratantonioDepartment of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari Aldo Moro, Via Orabona 4, 70125 Bari, Italy.ORCID 0000-0003-4835-0571
Gianluca BossiOncogenomic and Epigenetic Unit, Department of Diagnostic Research and Technological Innovation, IRCCS-Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144 Rome, Italy.ORCID 0000-0002-2947-1063

Funding

AIRC AIRC IG 2016 - ID. 18449Alice triangi" Pezcoller-Foundation fellowship 2019
6 · The paper itself

Abstract

Pharmacological treatment of colorectal carcinoma currently proceeds through the administration of a combination of different chemotherapeutic agents. In the case of rectal carcinoma, radiation therapy also represents a therapeutic strategy. In an attempt at translating much-needed new targeted therapy to the clinics, p38 mitogen activated protein kinase (MAPK) inhibitors have been tested in clinical trials involving colorectal carcinoma patients, especially in combination with chemotherapy; however, despite the high expectations raised by a clear involvement of the p38 MAPK pathway in the response to therapeutic treatments, poor results have been obtained so far. In this work, we review recent insights into the exact role of the p38 MAPK pathway in response to currently available therapies for colorectal carcinoma, depicting an intricate scenario in which the p38 MAPK node presents many opportunities, as well as many challenges, for its perspective exploitation for clinical purposes.

Indexed as

Antineoplastic AgentsApoptosisColorectal NeoplasmsFluorouracilHumansOxaliplatinp38 Mitogen-Activated Protein KinasesProtein IsoformsSignal TransductionAntineoplastic AgentsFluorouracilOxaliplatinp38 Mitogen-Activated Protein KinasesProtein Isoforms5-fluorouracilcolorectal canceririnotecanoxaliplatinp38 MAPKradiotherapytarget therapytherapeutic treatments

Identifiers

PMID32316313
PMCPMC7215415

What OpenQuestion holds

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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.