Evidence map›Paper›PMID 21586128›Full record

ArticleMolecular cancer2011

Natriuretic peptide receptor a as a novel target for prostate cancer.

Xiaoqin Wang, Payal Raulji, Shyam S Mohapatra, Ronil Patel, Gary Hellermann, Xiaoyuan Kong, Pedro L Vera, Katherine L Meyer-Siegler, Domenico Coppola, Subhra Mohapatra

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Is Atrial Natriuretic Peptide (ANP) and Natriuretic Peptide Receptor-A (NPR-A) Expression in Human Placenta and Decidua Normal?Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  7. Review
  8. Natriuretic Peptides: The Case of Prostate Cancer.Molecules (Basel, Switzerland) · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Natriuretic peptide receptor A as a novel target for cancer.World journal of surgical oncology · 2014
    Review
  13. Article
  14. Impact of NPR-A expression in gastric cancer cells.International journal of clinical and experimental medicine · 2014
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

10 authors at 4 institutions in 1 country.

Xiaoqin WangDepartment of Molecular Medicine, University of South Florida, Tampa, FL 33612, USA.
Payal Raulji
Shyam S Mohapatra
Ronil Patel
Gary Hellermann
Xiaoyuan Kong
Pedro L Vera
Katherine L Meyer-Siegler
Domenico Coppola
Subhra Mohapatra
University of South Florida · USBay Pines VA Healthcare System · USJames A. Haley Veterans' Hospital · USMoffitt Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
An Integrated Nano-Cell Delivery Platform of Theranostics for Lung CancersR01CA152005 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI MOHAPATRA, SHYAM S, MOHAPATRA, SUBHRA · 2010 to 2014
$1.4M
Nanomedicine Research Center Core (NRCC)P30HL101265 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI MOHAPATRA, SHYAM S · 2009 to 2010
$1.3M
Targeting of Curcumin-genistein nanocomplexes for Treatment of Prostate CancerR41CA139785 · NCI · TRANSGENEX NANOBIOTECH, INC. · PI MOHAPATRA, SUBHRA · 2009 to 2009
$159k
NCI NIH HHS CA139785NCI NIH HHS CA152005NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA152005NHLBI NIH HHS P30 HL101265
6 · The paper itself

Abstract

backgroundThe receptor for the cardiac hormone atrial natriuretic peptide (ANP), natriuretic peptide receptor A (NPRA), is expressed in cancer cells, and natriuretic peptides have been implicated in cancers. However, the direct role of NPRA signaling in prostate cancer remains unclear.

resultsNPRA expression was examined by western blotting, RT-PCR and immunohistochemistry. NPRA was downregulated by transfection of siRNA, shRNA and NPRA inhibitor (iNPRA). Antitumor efficacy of iNPRA was tested in mice using a TRAMP-C1 xenograft. Here, we demonstrated that NPRA is abundantly expressed on tumorigenic mouse and human prostate cells, but not in nontumorigenic prostate epithelial cells. NPRA expression showed positive correlation with clinical staging in a human PCa tissue microarray. Down-regulation of NPRA by siNPRA or iNPRA induced apoptosis in PCa cells. The mechanism of iNPRA-induced anti-PCa effects was linked to NPRA-induced expression of macrophage migration inhibitory factor (MIF), a proinflammatory cytokine over-expressed in PCa and significantly reduced by siNPRA. Prostate tumor cells implanted in mice deficient in atrial natriuretic peptide receptor A (NPRA-KO) failed to grow, and treatment of TRAMP-C1 xenografts with iNPRA reduced tumor burden and MIF expression. Using the TRAMP spontaneous PCa model, we found that NPRA expression correlated with MIF expression during PCa progression.

conclusionsCollectively, these results suggest that NPRA promotes PCa development in part by regulating MIF. Our findings also suggest that NPRA is a potential prognostic marker and a target for PCa therapy.

Indexed as

AnimalsApoptosisCell LineDisease ProgressionDown-RegulationHumansIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMaleMiceMice, Inbred C57BLMice, KnockoutPeptidesProstatic NeoplasmsRabbitsRatsatrial natriuretic factor receptor AIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humanPeptidesReceptors, Atrial Natriuretic FactorRNA, Small Interfering

Identifiers

PMID21586128
PMCPMC3121714
OpenAlexW2041408924

What OpenQuestion holds

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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.