Evidence map›Paper›PMID 24242705›Full record

ArticleClinical & experimental metastasis2014

Prostate cancer derived prostatic acid phosphatase promotes an osteoblastic response in the bone microenvironment.

Sandy R Larson, Jessica Chin, Xiaotun Zhang, Lisha G Brown, Ilsa M Coleman, Bryce Lakely, Martin Tenniswood, Eva Corey, Peter S Nelson, Robert L Vessella and 1 more

Open access · greenAbstract read
In one paragraph

Article in Clinical & experimental metastasis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Transmembrane prostatic acid phosphatase: a therapeutic target in advanced prostate cancer.American journal of clinical and experimental urology · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Hallmarks of Bone Metastasis.Calcified tissue international · 2018
    Review
  12. Hypercalcaemia and hypocalcaemia: finding the balance.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2017
    Review
  13. Article
  14. Review
  15. A review of osteocyte function and the emerging importance of sclerostin.The Journal of bone and joint surgery. American volume · 2014
    Review
  16. Article
  17. Prostate cancer and bone: the elective affinities.BioMed research international · 2014
    Review
  18. Review
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

11 authors at 3 institutions in 1 country.

Sandy R LarsonGenitourinary Cancer Research Laboratory, Department of Urology, University of Washington, Box 356510, Seattle, WA, 98195, USA.
Jessica Chin
Xiaotun Zhang
Lisha G Brown
Ilsa M Coleman
Bryce Lakely
Martin Tenniswood
Eva Corey
Peter S Nelson
Robert L Vessella
Colm Morrissey
University of Washington · USFred Hutch Cancer Center · USAlbany State University · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI John Kyung Lee · 2002 to 2026
$58.1M
Transmembrane Proteases and Prostate CarcinogenesisP01CA085859 · NCI · UNIVERSITY OF WASHINGTON · PI VESSELLA, ROBERT LOUIS · 2002 to 2013
$21.2M
NCI NIH HHS P01 CA085859NCI NIH HHS P01CA085859NCI NIH HHS P50 CA097186NCI NIH HHS P50CA97186
6 · The paper itself

Abstract

Approximately 90 % of patients who die of prostate cancer (PCa) have bone metastases, often promoting osteoblastic lesions. We observed that 88 % of castration-resistant PCa (CRPC) bone metastases express prostatic acid phosphatase (PAP), a soluble secreted protein expressed by prostate epithelial cells in predominately osteoblastic (n = 18) or osteolytic (n = 15) lesions. Additionally, conditioned media (CM) of an osteoblastic PCa xenograft LuCaP 23.1 contained significant levels of PAP and promoted mineralization in mouse and human calvaria-derived cells (MC3T3-E1 and HCO). To demonstrate that PAP promotes mineralization, we stimulated MC3T3-E1 cells with PAP and observed increased mineralization, which could be blocked with the specific PAP inhibitor, phosphonic acid. Furthermore, the mineralization promoted by LuCaP 23.1 CM was also blocked by phosphonic acid, suggesting PAP is responsible for the mineralization promoting activity of LuCaP 23.1. In addition, gene expression arrays comparing osteoblastic to osteolytic CRPC (n = 14) identified betacellulin (BTC) as a gene upregulated during the osteoblastic response in osteoblasts during new bone formation. Moreover, BTC levels were increased in bone marrow stromal cells in response to LuCaP 23.1 CM in vitro. Because new bone formation does occur in osteoblastic and can occur in osteolytic CRPC bone metastases, we confirmed by immunohistochemistry (n = 36) that BTC was highly expressed in osteoblasts involved in new bone formation occurring in both osteoblastic and osteolytic sites. These studies suggest a role for PAP in promoting the osteoblastic reaction in CRPC bone metastases and identify BTC as a novel downstream protein expressed in osteoblasts during new bone formation.

Indexed as

Tumor MicroenvironmentAcid PhosphataseBone and BonesBone NeoplasmsCell Line, TumorHumansMaleMass SpectrometryOsteoblastsProstatic NeoplasmsProtein Tyrosine PhosphatasesReverse Transcriptase Polymerase Chain ReactionAcid Phosphataseprostatic acid phosphataseProtein Tyrosine Phosphatases

Identifiers

PMID24242705
PMCPMC3946934
OpenAlexW2054783675

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.