Evidence map›Paper›PMID 17000760›Full record

ArticleMolecular and cellular biology2006

LZTS2 is a novel beta-catenin-interacting protein and regulates the nuclear export of beta-catenin.

Gregory Thyssen, Tzu-Huey Li, Lynn Lehmann, Ming Zhuo, Manju Sharma, Zijie Sun

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

47 citing papers in PubMed, 77 citations in OpenAlex.

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  10. Fine-Tuned Expression of Evolutionarily Conserved Signaling Molecules in theInternational journal of molecular sciences · 2024
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  12. Review
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  17. S-SCAM is essential for synapse formation.Frontiers in cellular neuroscience · 2023
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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 2 institutions in 1 country.

Gregory ThyssenDepartments of Urology and Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305-5118, USA.
Tzu-Huey Li
Lynn Lehmann
Ming Zhuo
Manju Sharma
Zijie Sun
Pediatrics and Genetics · USStanford University · US

Funding

Roles of the androgen receptor and its co-regulators in prostate tumorigenesisR01CA070297 · NCI · STANFORD UNIVERSITY · PI SUN, ZIJIE · 2003 to 2025
$5.0M
Beta-catenin and Androgen Signaling in Prostate CancerR01DK061002 · NIDDK · STANFORD UNIVERSITY · PI SUN, ZIJIE · 2003 to 2007
$1.7M
TGF-Beta/Smads and Androgen Signaling in Prostate CancerR01CA087767 · NCI · STANFORD UNIVERSITY · PI SUN, ZIJIE · 2002 to 2006
$1.3M
Cytokine control of hematopoiesis and leukemiasZ01DK061002 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI HENNIGHAUSEN, LOTHAR · 2007 to 2008
$1.1M
ANDROGEN RECEPTOR ASSOCIATED PROTEINS IN PROSTATE CANCERR29CA070297 · NCI · STANFORD UNIVERSITY · PI SUN, ZIJIE · 1997 to 2002
$329k
Androgen and Wnt Beta-catenin Signaling Pathways in Prostate CancerR56DK061002 · NIDDK · STANFORD UNIVERSITY · PI SUN, ZIJIE · 2008 to 2008
$36k
Intramural NIH HHS Z01 DK061002NCI NIH HHS CA 70297NCI NIH HHS CA 87767NCI NIH HHS R01 CA070297NCI NIH HHS R01 CA087767NCI NIH HHS R29 CA070297NIDDK NIH HHS DK 61002NIDDK NIH HHS R01 DK061002NIDDK NIH HHS R56 DK061002
6 · The paper itself

Abstract

Beta-catenin plays multiple roles in cell-cell adhesion and Wnt signal transduction. Through the Wnt signal, the cellular level of beta-catenin is constitutively regulated by the multicomponent destruction complex containing glycogen synthase kinase 3beta, axin, and adenomatous polyposis coli. Here, we present multiple lines of evidence to demonstrate that LZTS2 (lucine zipper tumor suppressor 2) interacts with beta-catenin, represses the transactivation of beta-catenin, and affects the subcellular localization of beta-catenin. The LZTS2 gene is located at 10q24.3, which is frequently lost in a variety of human tumors. A functional nuclear export signal (NES) was identified in the C terminus of the protein (amino acids 631 to 641). Appending this motif to green fluorescent protein (GFP) induced nuclear exclusion of the GFP fusion protein. However, introducing point mutations in either one or two leucine residues of this NES sequence abolished the nuclear exclusion of the LZTS2 protein. The nuclear export of LZTS2 can be blocked by leptomycin B (LMB), an inhibitor of the CRM1/exportin-alpha pathway. Intriguingly, beta-catenin colocalizes with LZTS2 in the cytoplasm of cells in the absence of LMB but in the nuclei of cells in the presence of LMB. Increasing the LZTS2 protein in cells reduces the level of nuclear beta-catenin in SW480 cells. Taken together, these data demonstrate that LZTS2 is a beta-catenin-interacting protein that can modulate beta-catenin signaling and localization.

Indexed as

Active Transport, Cell NucleusAmino Acid SequenceAnimalsbeta CateninCell Cycle ProteinsCell LineCell Line, TumorCell NucleusColonic NeoplasmsConserved SequenceDNA-Binding ProteinsFluorescent DyesGene Expression RegulationGlutathione TransferaseHaplorhiniHumansbeta CateninCell Cycle ProteinsDAPIDNA-Binding ProteinsFluorescent DyesGlutathione TransferaseIndolesLZTS2 protein, humanRecombinant Fusion ProteinsTumor Suppressor Proteins

Identifiers

PMID17000760
PMCPMC1636836
OpenAlexW1941492958

What OpenQuestion holds

Textmetadata
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.