Evidence map›Paper›PMID 30002193›Full record

ArticleMolecular cancer research : MCR2018

Tumor Suppressor Activity of Selenbp1, a Direct Nkx2-1 Target, in Lung Adenocarcinoma.

Deborah R Caswell, Chen-Hua Chuang, Rosanna K Ma, Ian P Winters, Eric L Snyder, Monte M Winslow

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

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  17. Brd4-bound enhancers drive cell-intrinsic sex differences in glioblastoma.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

6 authors at 3 institutions in 1 country.

Deborah R CaswellCancer Biology Program, Stanford University School of Medicine, Stanford, California.
Chen-Hua ChuangDepartment of Genetics, Stanford University School of Medicine, Stanford, California.
Rosanna K MaDepartment of Genetics, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-8980-8940
Ian P WintersDepartment of Genetics, Stanford University School of Medicine, Stanford, California.
Eric L SnyderDepartment of Pathology and Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.ORCID 0000-0003-3591-3195
Monte M WinslowCancer Biology Program, Stanford University School of Medicine, Stanford, California. mwinslow@stanford.edu.
Stanford University · USStanford Medicine · USHuntsman Cancer Institute · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Transcriptional Regulation of Lung Cancer IdentityR01CA212415 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Eric Lee Snyder · 2017 to 2026
$3.2M
Molecular Dissection of Lung Cancer Progression and MetastasisR01CA175336 · NCI · STANFORD UNIVERSITY · PI WINSLOW, MONTE MEIER · 2013 to 2017
$1.7M
Functional Interrogation of Kdm6a-Dependent Tumor Suppression during Pancreatic CancerF31CA210627 · NCI · STANFORD UNIVERSITY · PI WINTERS, IAN PAUL · 2016 to 2017
$64k
NCI NIH HHS F31 CA210627NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA175336NCI NIH HHS R01 CA212415NHGRI NIH HHS T32 HG000044
6 · The paper itself

Abstract

The Nkx2-1 transcription factor promotes differentiation of lung epithelial lineages and suppresses malignant progression of lung adenocarcinoma. However, targets of Nkx2-1 that limit tumor growth and progression remain incompletely understood. Here, direct Nkx2-1 targets are identified whose expression correlates with Nkx2-1 activity in human lung adenocarcinoma. Selenium-binding protein 1 (Selenbp1), an Nkx2-1 effector that limits phenotypes associated with lung cancer growth and metastasis, was investigated further. Loss- and gain-of-function approaches demonstrate that Nkx2-1 is required and sufficient for Selenbp1 expression in lung adenocarcinoma cells. Interestingly, Selenbp1 knockdown also reduced Nkx2-1 expression and Selenbp1 stabilized Nkx2-1 protein levels in a heterologous system, suggesting that these genes function in a positive feedback loop. Selenbp1 inhibits clonal growth and migration and suppresses growth of metastases in an

Indexed as

Adenocarcinoma of LungAnimalsCell Growth ProcessesCell Line, TumorCell MovementGene Expression Regulation, NeoplasticGene Knockdown TechniquesGenes, Tumor SuppressorHumansLung NeoplasmsMaleMiceSelenium-Binding ProteinsThyroid Nuclear Factor 1TransfectionNKX2-1 protein, humanNkx2-1 protein, mouseSELENBP1 protein, humanSelenbp1 protein, mouseSelenium-Binding ProteinsThyroid Nuclear Factor 1

Identifiers

PMID30002193
PMCPMC6541221
OpenAlexW2879968231

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.