Evidence map›Paper›PMID 34022881›Full record

ReviewCell communication and signaling : CCS2021

Role of the ABL tyrosine kinases in the epithelial-mesenchymal transition and the metastatic cascade.

Jillian Hattaway Luttman, Ashley Colemon, Benjamin Mayro, Ann Marie Pendergast

Open access · goldAbstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Jillian Hattaway LuttmanDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, 308 Research Drive, C-233A LSRC Bldg., P.O. Box 3813, Durham, NC, 27710, USA.
Ashley ColemonDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, 308 Research Drive, C-233A LSRC Bldg., P.O. Box 3813, Durham, NC, 27710, USA.
Benjamin MayroDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, 308 Research Drive, C-233A LSRC Bldg., P.O. Box 3813, Durham, NC, 27710, USA.
Ann Marie PendergastDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, 308 Research Drive, C-233A LSRC Bldg., P.O. Box 3813, Durham, NC, 27710, USA. ann.pendergast@duke.edu.ORCID 0000-0002-1250-6880
Duke University · US

Funding

Targeted Alpha-Particle Radiotheraphy of Brain Tumors with 211At-81C6 AntibodyP50CA190991 · NCI · DUKE UNIVERSITY · PI SAMPSON, JOHN H. · 2014 to 2023
$20.8M
Pharmacological Sciences Training ProgramT32GM007105 · NIGMS · DUKE UNIVERSITY · PI KUHN, CYNTHIA M · 1985 to 2019
$9.0M
Targeting tumor-neural cell interactions to inhibit lung cancer brain metastasisR01CA246133 · NCI · DUKE UNIVERSITY · PI PENDERGAST, ANN MARIE · 2021 to 2025
$2.2M
Novel target for therapy refractory lung tumorsR01CA195549 · NCI · DUKE UNIVERSITY · PI PENDERGAST, ANN MARIE · 2015 to 2019
$1.8M
Understanding the impact that tumor representative oxygen tension has on phosphotyrosine-dependent signaling networks in solid tumorsF99CA264162 · NCI · DUKE UNIVERSITY · PI MAYRO, BENJAMIN JACOB · 2021 to 2022
$78k
ABL kinases promote lung cancer brain metastasis through regulation of transcriptional networksF31CA243293 · NCI · DUKE UNIVERSITY · PI MAYRO, BENJAMIN JACOB · 2020 to 2020
$37k
NCI NIH HHS F31 CA243293NCI NIH HHS F99 CA264162NCI NIH HHS P50 CA190991NCI NIH HHS R01 CA195549NCI NIH HHS R01 CA246133NIGMS NIH HHS T32 GM007105NIH HHS 5T32GM007105-44
6 · The paper itself

Abstract

The ABL kinases, ABL1 and ABL2, promote tumor progression and metastasis in various solid tumors. Recent reports have shown that ABL kinases have increased expression and/or activity in solid tumors and that ABL inactivation impairs metastasis. The therapeutic effects of ABL inactivation are due in part to ABL-dependent regulation of diverse cellular processes related to the epithelial to mesenchymal transition and subsequent steps in the metastatic cascade. ABL kinases target multiple signaling pathways required for promoting one or more steps in the metastatic cascade. These findings highlight the potential utility of specific ABL kinase inhibitors as a novel treatment paradigm for patients with advanced metastatic disease. Video abstract.

Indexed as

Epithelial-Mesenchymal TransitionCytoskeletonDisease ProgressionHumansMolecular Targeted TherapyNeoplasm MetastasisProto-Oncogene Proteins c-ablProto-Oncogene Proteins c-ablABL kinasesEMTMetastasisSignaling

Identifiers

PMID34022881
PMCPMC8140471
OpenAlexW3164628319

What Socratic 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 Socratic graph.