Evidence map›Paper›PMID 24668563›Full record

ArticleCancer2014

Elevated hyaluronan and hyaluronan-mediated motility receptor are associated with biochemical failure in patients with intermediate-grade prostate tumors.

Anthony E Rizzardi, Rachel Isaksson Vogel, Joseph S Koopmeiners, Colleen L Forster, Lauren O Marston, Nikolaus K Rosener, Natalia Akentieva, Matthew A Price, Gregory J Metzger, Christopher A Warlick and 4 more

Abstract read
In one paragraph

Article in Cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
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  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Hyaluronan heterogeneity in pancreatic ductal adenocarcinoma: Primary tumors compared to sites of metastasis.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2022
    Article
  12. Article
  13. RHAMM Is a Multifunctional Protein That Regulates Cancer Progression.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
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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

14 authors at 5 institutions in 2 countries.

Anthony E RizzardiDepartment of Pathology, University of Washington, Seattle, Washington; Department of Laboratory Medicine and Pathology and Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Rachel Isaksson Vogel
Joseph S Koopmeiners
Colleen L Forster
Lauren O Marston
Nikolaus K Rosener
Natalia Akentieva
Matthew A Price
Gregory J Metzger
Christopher A Warlick
Jonathan C Henriksen
Eva A Turley
James B McCarthy
Stephen C Schmechel
University of Minnesota · USUniversity of Minnesota Medical Center · USUniversity of Minnesota System · USWestern University · CAUniversity of Washington · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
Virological Measurements of Cryptic ReplicationP01AI074340 · NIAID · UNIVERSITY OF MINNESOTA · PI SCHACKER, TIMOTHY W · 2008 to 2012
$12.1M
UAB / UMN SPORE in Pancreatic CancerP50CA101955 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUCHSBAUM, DONALD J · 2010 to 2014
$11.1M
Antifibrotic Therapy to Improve Immune reconstitution in HIVR01AI093319 · NIAID · UNIVERSITY OF MINNESOTA · PI SCHACKER, TIMOTHY W · 2011 to 2014
$2.8M
Hyaluronan Receptors in Prostate Cancer ProgressionR01CA119092 · NCI · UNIVERSITY OF MINNESOTA · PI MCCARTHY, JAMES B. · 2008 to 2012
$2.2M
Multi-parametric MRI Determination of Prostate Cancer Aggressiveness and ExtentR01CA131013 · NCI · UNIVERSITY OF MINNESOTA · PI METZGER, GREGORY JOHN · 2008 to 2012
$1.6M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)KL2RR033182 · NCRR · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2011 to 2011
$1.4M
NCATS NIH HHS UL1 TR000114NCI NIH HHS P30 CA077598NCI NIH HHS P30-CA77598NCI NIH HHS P50 CA101955NCI NIH HHS P50-CA101955NCI NIH HHS R01 CA119092NCI NIH HHS R01-CA119092NCI NIH HHS R01 CA131013NCI NIH HHS R01-CA131013NCRR NIH HHS KL2 RR033182NCRR NIH HHS KL2-RR033182NIAID NIH HHS P01 AI074340NIAID NIH HHS P01-AI074340NIAID NIH HHS R01 AI093319NIAID NIH HHS R01-AI093319
6 · The paper itself

Abstract

backgroundThe clinical course of prostate cancer (PCa) measured by biochemical failure (BF) after prostatectomy remains unpredictable in many patients, particularly in intermediate Gleason score (GS) 7 tumors, suggesting that identification of molecular mechanisms associated with aggressive PCa biology may be exploited for improved prognostication or therapy. Hyaluronan (HA) is a high molecular weight polyanionic carbohydrate produced by synthases (HAS1 through HAS3) and fragmented by oxidative/nitrosative stress and hyaluronidases (HYAL1 through HYAL4, SPAM1) common in PCa microenvironments. HA and HA fragments interact with receptors CD44 and hyaluronan-mediated motility receptor (HMMR), resulting in increased tumor aggressiveness in experimental PCa models. This study evaluated the association of HA-related molecules with BF after prostatectomy in GS7 tumors.

methodsTissue microarrays were constructed from a 96-patient cohort. HA histochemistry and HAS2, HYAL1, CD44, CD44v6, and HMMR immunohistochemistry were quantified using digital pathology techniques.

resultsHA in tumor-associated stroma and HMMR in malignant epithelium were significantly and marginally significantly associated with time to BF in univariate analysis, respectively. After adjusting for clinicopathologic features, both HA in tumor-associated stroma and HMMR in malignant epithelium were significantly associated with time to BF. Although not significantly associated with BF, HAS2 and HYAL1 positively correlated with HMMR in malignant epithelium. Cell culture assays demonstrated that HMMR bound native and fragmented HA, promoted HA uptake, and was required for a promigratory response to fragmented HA.

conclusionsHA and HMMR are factors associated with time to BF in GS7 tumors, suggesting that increased HA synthesis and fragmentation within the tumor microenvironment stimulates aggressive PCa behavior through HA-HMMR signaling.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorCell MovementCohort StudiesExtracellular Matrix ProteinsHEK293 CellsHumansHyaluronan ReceptorsHyaluronic AcidImmunohistochemistryMaleMiceMice, Inbred C3HNeoplasm GradingPrognosisBiomarkers, TumorExtracellular Matrix Proteinshyaluronan-mediated motility receptorHyaluronan ReceptorsHyaluronic Acidbiomarkersdigital pathologyhyaluronanhyaluronan-mediated motility receptorprostate cancer

Identifiers

PMID24668563
PMCPMC4047165
OpenAlexW1544256999

What OpenQuestion holds

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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.