Evidence map›Paper›PMID 33045253›Full record

ReviewPharmacology & therapeutics2021

The regulatory function of mixed lineage kinase 3 in tumor and host immunity.

Sandeep Kumar, Sunil Kumar Singh, Basabi Rana, Ajay Rana

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. MLK3 promotes atherosclerosis by regulating ferroptosis in macrophages.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Review
  3. Article
  4. Infectious Diseases.Advances in neurobiology · 2024
    Review
  5. 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.

Sandeep KumarDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA. Electronic address: ksandeep@uic.edu.
Sunil Kumar SinghDepartment 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; University of Illinois Hospital & Health Sciences System Cancer Center, University of Illinois at Chicago, Chicago, IL 60612, USA; Jesse Brown VA Medical Center, Chicago, IL 60612, USA.
Ajay RanaDepartment of Surgery, Division of Surgical Oncology, University of Illinois at Chicago, IL 60612, USA; University of Illinois Hospital & Health Sciences System Cancer Center, University of Illinois at Chicago, Chicago, IL 60612, USA; Jesse Brown VA Medical Center, Chicago, IL 60612, USA. Electronic address: arana@uic.edu.
Jesse Brown VA Medical Center · USUniversity of Illinois Chicago · 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
Role of beta-catenin in apoptosis resistance of hepatocellular carcinomaR01CA178063 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RANA, BASABI · 2014 to 2018
$1.6M
Mechanistic Insight on the Role of Berberine and AMPK in Hepatocellular CarcinomaR03CA219764 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RANA, BASABI · 2019 to 2020
$160k
Elucidation of MLK3 Signaling in Hepatocellular CarcinomaI01BX003296 · VA · JESSE BROWN VA MEDICAL CENTER · PI RANA, BASABI · 2016 to 2022
–
BLR&D Research Career Scientist Award ApplicationIK6BX004855 · VA · JESSE BROWN VA MEDICAL CENTER · PI AJAY NMN RANA · 2020 to 2026
–
BLRD VA I01 BX003296BLRD VA I01 BX004903BLRD VA IK6 BX004855NCI NIH HHS R01 CA178063NCI NIH HHS R01 CA216410NCI NIH HHS R03 CA219764
6 · The paper itself

Abstract

Protein kinases are the second most sought-after G-protein coupled receptors as drug targets because of their overexpression, mutations, and dysregulated catalytic activities in various pathological conditions. Till 2019, 48 protein kinase inhibitors have received FDA approval for the treatment of multiple illnesses, of which the majority of them are indicated for different malignancies. One of the attractive sub-group of protein kinases that has attracted attention for drug development is the family members of MAPKs that are recognized to play significant roles in different cancers. Several inhibitors have been developed against various MAPK members; however, none of them as monotherapy has shown sustainable efficacy. One of the MAPK members, called Mixed Lineage Kinase 3 (MLK3), has attracted considerable attention due to its role in inflammation and neurodegenerative diseases; however, its role in cancer is an emerging area that needs more investigation. Recent advances have shown that MLK3 plays a role in cancer cell survival, migration, drug resistance, cell death, and tumor immunity. This review describes how MLK3 regulates different MAPK pathways, cancer cell growth and survival, apoptosis, and host's immunity. We also discuss how MLK3 inhibitors can potentially be used along with immunotherapy for different malignancies.

Indexed as

MAP Kinase Kinase KinasesNeoplasmsApoptosisCell Transformation, NeoplasticHumansMitogen-Activated Protein Kinase Kinase Kinase 11MAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11Adaptive immunityCancerImmunotherapyInnate immunityMitogen-activated protein kinaseMixed lineage kinase 3T cell

Identifiers

PMID33045253
PMCPMC7887016
OpenAlexW3092259317

What OpenQuestion holds

Textmetadata
LicenceTDM
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.