Evidence map›Paper›PMID 26239765›Full record

ArticleJournal of cellular biochemistry2016

Schwann Cells Increase Prostate and Pancreatic Tumor Cell Invasion Using Laminin Binding A6 Integrin.

Isis C Sroka, Harsharon Chopra, Lipsa Das, Jaime M C Gard, Raymond B Nagle, Anne E Cress

Abstract read
In one paragraph

Article in Journal of cellular biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  3. Integrins as key regulators in tumor perineural invasion: mechanisms and clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  9. Integrated multi-omics elucidatesFrontiers in immunology · 2025
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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 1 institution in 1 country.

Isis C SrokaDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona, 85724.
Harsharon ChopraDepartment of Pathology, University of Arizona College of Medicine, Tucson, Arizona, 85724.
Lipsa DasUniversity of Arizona Cancer Center, 1515 North Campbell Avenue, Tucson, Arizona, 85724.
Jaime M C GardUniversity of Arizona Cancer Center, 1515 North Campbell Avenue, Tucson, Arizona, 85724.
Raymond B NagleDepartment of Pathology, University of Arizona College of Medicine, Tucson, Arizona, 85724.
Anne E CressUniversity of Arizona Cancer Center, 1515 North Campbell Avenue, Tucson, Arizona, 85724.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Integrative Cancer Scholars Training GrantT32CA009213 · NCI · UNIVERSITY OF ARIZONA · PI CAREW, JENNIFER S, CURIEL-LEWANDROWSKI, CLARA · 1985 to 2024
$8.6M
Human Prostate Cancer Metastasis and Laminin Binding IntegrinsR01CA159406 · NCI · UNIVERSITY OF ARIZONA · PI CRESS, ANNE E · 2011 to 2015
$1.5M
Mechanisms of Pancreatic Tumor Nerve InvasionR03CA164484 · NCI · UNIVERSITY OF ARIZONA · PI SROKA, ISIS C · 2012 to 2013
$152k
NCI NIH HHS P30 CA023074NCI NIH HHS P30 CA23074NCI NIH HHS R01 CA159406NCI NIH HHS R03 CA164484NCI NIH HHS T32 CA009213NCI NIH HHS T32 CA09213
6 · The paper itself

Abstract

Human pancreatic and prostate cancers metastasize along nerve axons during perineural invasion. The extracellular matrix laminin class of proteins is an abundant component of both myelinated and non-myelinated nerves. Analysis of human pancreatic and prostate tissue revealed both perineural and endoneural invasion with Schwann cells surrounded or disrupted by tumor, respectively. Tumor and nerve cell co-culture conditions were used to determine if myelinating or non-myelinating Schwann cell (S16 and S16Y, respectively) phenotype was equally likely to promote integrin-dependent cancer cell invasion and migration on laminin. Conditioned medium from S16 cells increased tumor cell (DU145, PC3, and CFPAC1) invasion into laminin approximately 1.3-2.0 fold compared to fetal bovine serum (FBS) treated cells. Integrin function (e.g., ITGA6p formation) increased up to 1.5 fold in prostate (DU145, PC3, RWPE-1) and pancreatic (CFPAC1) cells, and invasion was dependent on ITGA6p formation and ITGB1 as determined by function-blocking antibodies. In contrast, conditioned medium isolated from S16Y cells (non-myelinating phenotype) decreased constitutive levels of ITGA6p in the tumor cells by 50% compared to untreated cells and decreased ITGA6p formation 3.0 fold compared to S16 treated cells. Flow cytometry and western blot analysis revealed loss of ITGA6p formation as reversible and independent of overall loss of ITGA6 expression. These results suggest that the myelinating phenotype of Schwann cells within the tumor microenvironment increased integrin-dependent tumor invasion on laminin.

Indexed as

Cell Line, TumorCell MovementCoculture TechniquesGene Expression Regulation, NeoplasticHumansIntegrin alpha6Integrin beta1MaleNeoplasm InvasivenessPancreatic NeoplasmsProstatic NeoplasmsSchwann CellsIntegrin alpha6Integrin beta1ITGA6 protein, humanA6B1LAMININMETASTASISMICROENVIRONMENTPERINEURAL INVASIONSCHWANN CELLS

Identifiers

PMID26239765
PMCPMC4809241
OpenAlexW1837051231

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.