Evidence map›Paper›PMID 29782621›Full record

ArticleCommunications biology2018

DARPP-32 and t-DARPP promote non-small cell lung cancer growth through regulation of IKKα-dependent cell migration.

Sk Kayum Alam, Matteo Astone, Ping Liu, Stephanie R Hall, Abbygail M Coyle, Erin N Dankert, Dane K Hoffman, Wei Zhang, Rui Kuang, Anja C Roden and 2 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  8. Intrinsic epigenetic state of primary osteosarcoma drives metastasis.bioRxiv : the preprint server for biology · 2023
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  11. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Sk Kayum AlamThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA.ORCID http://orcid.org/0000-0001-5342-4542
Matteo AstoneThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA.
Ping LiuDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA.
Stephanie R HallThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA.
Abbygail M CoyleThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA.ORCID http://orcid.org/0000-0003-1068-4939
Erin N DankertThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA.ORCID http://orcid.org/0000-0003-1424-0155
Dane K HoffmanDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0002-3934-4770
Wei ZhangDepartment of Computer Science and Engineering, University of Minnesota, Minneapolis, MN, 55455, USA.ORCID http://orcid.org/0000-0003-3605-9373
Rui KuangDepartment of Computer Science and Engineering, University of Minnesota, Minneapolis, MN, 55455, USA.
Anja C RodenDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Aaron S MansfieldDepartment of Oncology, Division of Medical Oncology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0002-9483-6903
Luke H HoeppnerThe Hormel Institute, University of Minnesota, Austin, MN, 55912, USA. lhoeppner@hi.umn.edu.ORCID http://orcid.org/0000-0003-3948-4244
University of Minnesota · USMayo Clinic · USMayo Clinic in Arizona · US

Funding

Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
Triggering the dopamine pathway to inhibit lung cancer progressionR00CA187035 · NCI · UNIVERSITY OF MINNESOTA · PI HOEPPNER, LUKE HILBERT · 2015 to 2017
$743k
NCI NIH HHS K12 CA090628NCI NIH HHS R00 CA187035
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related death worldwide. Here we demonstrate that elevated expression of dopamine and cyclic adenosine monophosphate-regulated phosphoprotein, Mr 32000 (DARPP-32) and its truncated splice variant t-DARPP promote lung tumor growth, while abrogation of DARPP-32 expression in human non-small cell lung cancer (NSCLC) cells reduces tumor growth in orthotopic mouse models. We observe a novel physical interaction between DARPP-32 and inhibitory kappa B kinase-α (IKKα) that promotes NSCLC cell migration through non-canonical nuclear factor kappa-light-chain-enhancer of activated B cells 2 (NF-κB2) signaling. Bioinformatics analysis of 513 lung adenocarcinoma patients reveals elevated t-DARPP isoform expression is associated with poor overall survival. Histopathological investigation of 62 human lung adenocarcinoma tissues also shows that t-DARPP expression is elevated with increasing tumor (T) stage. Our data suggest that DARPP-32 isoforms serve as a negative prognostic marker associated with increasing stages of NSCLC and may represent a novel therapeutic target.

Indexed as

AktcancerDARPP-32ErkIKKαmigrationNF-κB2NSCLCsurvivalt-DARPP

Identifiers

PMID29782621
PMCPMC5959014
OpenAlexW2800924700

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.