Evidence map›Paper›PMID 31936067›Full record

ReviewPharmaceuticals (Basel, Switzerland)2020

Mitogen-Activated Protein Kinase Inhibitors and T-Cell-Dependent Immunotherapy in Cancer.

Sandeep Kumar, Daniel R Principe, Sunil Kumar Singh, Navin Viswakarma, Gautam Sondarva, Basabi Rana, Ajay Rana

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  10. Review
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  13. Article
  14. Small-Molecule PROTACs for Cancer Immunotherapy.Molecules (Basel, Switzerland) · 2022
    Review
  15. Article
  16. Article
  17. Article
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  19. Review
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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.

Sandeep KumarDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
Daniel R PrincipeDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
Sunil Kumar SinghDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
Navin ViswakarmaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.ORCID 0000-0001-9837-2619
Gautam SondarvaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
Basabi RanaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
Ajay RanaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA.
University of Illinois Chicago · USIllinois College · US

Funding

Developing Nano Technology for HER2 Directed TherapyR01CA216410 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LI, SONG, RANA, AJAY NMN · 2017 to 2021
$2.8M
Oncogenic MLK3-Pak1 Signaling in ER Negative Breast CancerR01CA176846 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RANA, AJAY NMN · 2013 to 2017
$1.6M
Role of beta-catenin in apoptosis resistance of hepatocellular carcinomaR01CA178063 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RANA, BASABI · 2014 to 2018
$1.6M
Augmenting Pancreatic Cancer Immunotherapy via TGFβ Pathway InhibitionF30CA236031 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRINCIPE, DANIEL R · 2019 to 2023
$256k
Elucidation of MLK3 Signaling in Hepatocellular CarcinomaI01BX003296 · VA · JESSE BROWN VA MEDICAL CENTER · PI RANA, BASABI · 2016 to 2022
–
BLRD VA I01 BX003296NCI NIH HHS CA 176846NCI NIH HHS CA178063NCI NIH HHS CA 216410NCI NIH HHS F30 CA236031NCI NIH HHS R01 CA178063NIH HHS 1F30CA236031U.S. Department of Veterans Affairs BX002703U.S. Department of Veterans Affairs BX003296
6 · The paper itself

Abstract

Mitogen-activated protein kinase (MAPK) signaling networks serve to regulate a wide range of physiologic and cancer-associated cell processes. For instance, a variety of oncogenic mutations often lead to hyperactivation of MAPK signaling, thereby enhancing tumor cell proliferation and disease progression. As such, several components of the MAPK signaling network have been proposed as viable targets for cancer therapy. However, the contributions of MAPK signaling extend well beyond the tumor cells, and several MAPK effectors have been identified as key mediators of the tumor microenvironment (TME), particularly with respect to the local immune infiltrate. In fact, a blockade of various MAPK signals has been suggested to fundamentally alter the interaction between tumor cells and T lymphocytes and have been suggested a potential adjuvant to immune checkpoint inhibition in the clinic. Therefore, in this review article, we discuss the various mechanisms through which MAPK family members contribute to T-cell biology, as well as circumstances in which MAPK inhibition may potentiate or limit cancer immunotherapy.

Indexed as

cancercytotoxic T-lymphocyte-associated protein 4immunotherapymitogen-activated protein kinaseProgrammed cell death protein 1Programmed death-ligand 1T-cell anergyT cells

Identifiers

PMID31936067
PMCPMC7168889
OpenAlexW3000522286

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.