Evidence map›Paper›PMID 22927397›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Secreted protein, acidic and rich in cysteine-like 1 (SPARCL1) is down regulated in aggressive prostate cancers and is prognostic for poor clinical outcome.

Paula J Hurley, Luigi Marchionni, Brian W Simons, Ashley E Ross, Sarah B Peskoe, Rebecca M Miller, Nicholas Erho, Ismael A Vergara, Mercedeh Ghadessi, Zhenhua Huang and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 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

17 authors at 5 institutions in 2 countries.

Paula J HurleyDepartment of Urology, The Johns Hopkins University, Baltimore, MD 21231, USA. phurley2@jhmi.edu
Luigi Marchionni
Brian W Simons
Ashley E Ross
Sarah B Peskoe
Rebecca M Miller
Nicholas Erho
Ismael A Vergara
Mercedeh Ghadessi
Zhenhua Huang
Bora Gurel
Ben Ho Park
Elai Davicioni
Robert B Jenkins
Elizabeth A Platz
David M Berman
Edward M Schaeffer
Johns Hopkins University · USGenome British Columbia · CASidney Kimmel Comprehensive Cancer Center · USMayo Clinic · USQueen's University · CA

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA006973NCI NIH HHS P30CA006973
6 · The paper itself

Abstract

Prostate cancer is the second leading cause of cancer death among United States men. However, disease aggressiveness is varied, with low-grade disease often being indolent and high-grade cancer accounting for the greatest density of deaths. Outcomes are also disparate among men with high-grade prostate cancer, with upwards of 65% having disease recurrence even after primary treatment. Identification of men at risk for recurrence and elucidation of the molecular processes that drive their disease is paramount, as these men are the most likely to benefit from multimodal therapy. We previously showed that androgen-induced expression profiles in prostate development are reactivated in aggressive prostate cancers. Herein, we report the down-regulation of one such gene, Sparcl1, a secreted protein, acidic and rich in cysteine (SPARC) family matricellular protein, during invasive phases of prostate development and regeneration. We further demonstrate a parallel process in prostate cancer, with decreased expression of SPARCL1 in high-grade/metastatic prostate cancer. Mechanistically, we demonstrate that SPARCL1 loss increases the migratory and invasive properties of prostate cancer cells through Ras homolog gene family, member C (RHOC), a known mediator of metastatic progression. By using models incorporating clinicopathologic parameters to predict prostate cancer recurrence after treatment, we show that SPARCL1 loss is a significant, independent prognostic marker of disease progression. Thus, SPARCL1 is a potent regulator of cell migration/invasion and its loss is independently associated with prostate cancer recurrence.

Indexed as

AnimalsCalcium-Binding ProteinsCell Line, TumorCell MovementDisease ProgressionDNA PrimersExtracellular Matrix ProteinsFlow CytometryFluorescent Antibody TechniqueGene Expression Regulation, NeoplasticHumansImmunoblottingImmunohistochemistryMaleMiceMice, Mutant StrainsCalcium-Binding ProteinsDNA PrimersExtracellular Matrix ProteinsrhoC GTP-Binding ProteinRHOC protein, humanrho GTP-Binding ProteinsSPARCL1 protein, humanTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID22927397
PMCPMC3443123
OpenAlexW2059057645

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.