Evidence map›Paper›PMID 16004602›Full record

ArticleThe Biochemical journal2005

The Rab27a-binding protein, JFC1, regulates androgen-dependent secretion of prostate-specific antigen and prostatic-specific acid phosphatase.

Jennifer L Johnson, Beverly A Ellis, Deborah Noack, Miguel C Seabra, Sergio D Catz

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Therapeutic targeting of neutrophil exocytosis.Journal of leukocyte biology · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Human prostatic acid phosphatase: structure, function and regulation.International journal of molecular sciences · 2013
    Review
  14. Article
  15. Article
  16. Rab GTPases implicated in inherited and acquired disorders.Seminars in cell & developmental biology · 2011
    Review
  17. Estrogen regulates vesicle trafficking gene expression in EFF-3, EFM-19 and MCF-7 breast cancer cells.International journal of clinical and experimental pathology · 2009
    Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 2 countries.

Jennifer L JohnsonDivision of Biochemistry, Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Beverly A Ellis
Deborah Noack
Miguel C Seabra
Sergio D Catz
Scripps Research Institute · USImperial College London · GB

Funding

THE FUNCTION OF NORMAL AND MALIGNANT PHAGOCYTESR01AI024227 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CATZ, SERGIO DANIEL · 1985 to 2007
$4.0M
P56C2, A NOVEL C2 DOMAIN PROTEIN OF LEUKOCYTESR01AI044434 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI BABIOR, BERNARD M · 1999 to 2003
$1.4M
FUNCTION OF NORMAL AND MALIGNANT PHAGOCYTESR37AI024227 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI BABIOR, BERNARD M · 1988 to 1997
–
NIAID NIH HHS AI-024227NIAID NIH HHS AI-044434NIAID NIH HHS R01 AI024227
6 · The paper itself

Abstract

Two of the major proteins secreted by the prostate epithelium secretory cells are PSA (prostate-specific antigen) and PSAP (prostatic-specific acid phosphatase). The molecules involved in the secretory machinery of PSA and PSAP, and the regulation of this machinery, remain unknown. In the present paper, we provide evidence that JFC1 [synaptotagmin-like protein (slp1)], a Rab27a- and PtdIns(3,4,5)P3-binding protein, regulates the androgen-dependent secretion of PSAP and PSA in human LNCaP prostate carcinoma cells. Androgen-dependent PSAP secretion was significantly inhibited in cells that expressed the C2A domain of JFC1 [PtdIns(3,4,5)P3-binding-domain], but was unaffected by JFC1 overexpression. Conversely, PSA secretion was not inhibited by the C2A domain of JFC1. We show, using immunofluorescence analysis, that JFC1 co-localizes with PSAP, but rarely with PSA, in prostate granules, suggesting that JFC1 is part of the PSAP secretory machinery. However, PSA secretion was significantly increased in LNCaP cells that overexpressed JFC1, indicating that the secretion of PSA is susceptible to variations in the intracellular concentration of JFC1. Both PSAP and PSA secretion was increased by overexpression of wild-type Rab27a or the constitutively active Rab27aQ78L. The secretion of PSA was partially inhibited in the presence of LY294002, while the secretion of PSAP was completely abolished by the PI3K (phosphoinositide 3-kinase) inhibitor. This supports the view that PI3K plays a differential role in the secretion of prostate secretory markers. In conclusion, we present evidence that JFC1 differentially regulates the secretion of PSAP and PSA, and that Rab27a and PI3K play a central role in the exocytosis of prostate-specific markers.

Indexed as

Acid PhosphataseAndrogensCell Line, TumorCytoplasmic GranulesGene Expression Regulation, EnzymologicHumansMaleMembrane ProteinsPhosphatidylinositol 3-KinasesProstateProstate-Specific AntigenProtein BindingProtein TransportProtein Tyrosine Phosphatasesrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsAcid PhosphataseAndrogensMembrane ProteinsPhosphatidylinositol 3-KinasesProstate-Specific Antigenprostatic acid phosphataseProtein Tyrosine PhosphatasesRAB27A protein, humanrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsSYTL1 protein, humanTestosterone

Identifiers

PMID16004602
PMCPMC1276972
OpenAlexW2151188524

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.