Evidence map›Paper›PMID 26934365›Full record

ArticlePloS one2016

Calcitonin Receptor-Zonula Occludens-1 Interaction Is Critical for Calcitonin-Stimulated Prostate Cancer Metastasis.

Ahmed Aljameeli, Arvind Thakkar, Shibu Thomas, Vijaybasker Lakshmikanthan, Kenneth A Iczkowski, Girish V Shah

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 20 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

6 authors at 3 institutions in 1 country.

Ahmed AljameeliPharmacology, University of Louisiana College of Pharmacy, Monroe, LA 71201, United States of America.
Arvind ThakkarPharmacology, University of Louisiana College of Pharmacy, Monroe, LA 71201, United States of America.
Shibu ThomasPharmacology, University of Louisiana College of Pharmacy, Monroe, LA 71201, United States of America.
Vijaybasker LakshmikanthanPharmacology, University of Louisiana College of Pharmacy, Monroe, LA 71201, United States of America.
Kenneth A IczkowskiPathology, Medical College of Wisconsin, Madison, WI 53226, United States of America.
Girish V ShahPharmacology, University of Louisiana College of Pharmacy, Monroe, LA 71201, United States of America.
Louisiana Christian University · USUniversity of Louisiana at Monroe · USMedical College of Wisconsin · US

Funding

Calcitonin in Prostate Growth and NeplasiaR01CA096534 · NCI · UNIVERSITY OF LOUISIANA AT MONROE · PI SHAH, GIRISH V · 2001 to 2013
$1.4M
Calcitonin in Prostate Growth and NeoplasiaR56CA096534 · NCI · UNIVERSITY OF LOUISIANA AT MONROE · PI SHAH, GIRISH V · 2008 to 2008
$175k
NCI NIH HHS NIH CA096534NCI NIH HHS R01 CA096534NCI NIH HHS R56 CA096534
6 · The paper itself

Abstract

The role of neuroendocrine peptide calcitonin (CT) and its receptor (CTR) in epithelial cancer progression is an emerging concept with great clinical potential. Expression of CT and CTR is frequently elevated in prostate cancers (PCs) and activation of CT-CTR axis in non-invasive PC cells induces an invasive phenotype. Here we show by yeast-two hybrid screens that CTR associates with the tight junction protein Zonula Occludens-1 (ZO-1) via the interaction between the type 1 PDZ motif at the carboxy-terminus of CTR and the PDZ3 domain of ZO-1. Mutation of either the CTR C-PDZ-binding motif or the ZO-1-PDZ3 domain did not affect binding of CTR with its ligand or G-protein-mediated signaling but abrogated destabilizing actions of CT on tight junctions and formation of distant metastases by orthotopically implanted PC cells in nude mice, indicating that these PDZ domain interactions were pathologically relevant. Further, we observed CTR-ZO-1 interactions in PC specimens by proximity ligation immunohistochemistry, and identified that the number of interactions in metastatic PC specimens was several-fold larger than in non-metastatic PC. Our results for the first time demonstrate a mechanism by which PDZ-mediated interaction between CTR and ZO1 is required for CT-stimulated metastasis of prostate cancer. Since many receptors contain PDZ-binding motifs, this would suggest that PDZ-binding motif-adaptor protein interactions constitute a common mechanism for cancer metastasis.

Indexed as

AnimalsCalcitoninCell Line, TumorHumansMaleMiceMice, Inbred BALB CMice, NudeNeoplasm MetastasisPDZ DomainsProstatic NeoplasmsProtein BindingProtein Interaction Domains and MotifsReceptors, CalcitoninSignal TransductionTight JunctionsCalcitoninReceptors, CalcitoninZonula Occludens-1 Protein

Identifiers

PMID26934365
PMCPMC4775073
OpenAlexW2294673744

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.