Evidence map›Paper›PMID 23255611›Full record

ArticleThe Journal of biological chemistry2013

Type 10 soluble adenylyl cyclase is overexpressed in prostate carcinoma and controls proliferation of prostate cancer cells.

Jan-Paul Flacke, Hanna Flacke, Avinash Appukuttan, Rein-Jüri Palisaar, Joachim Noldus, Brian D Robinson, H Peter Reusch, Jonathan H Zippin, Yury Ladilov

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. 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
1.7field-weighted citation impact, top 16% 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, 52 citations in OpenAlex.

  1. Review
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  10. Article
  11. Cell Metabolism and DNA Repair Pathways: Implications for Cancer Therapy.Frontiers in cell and developmental biology · 2021
    Review
  12. Cross-Talk Between the Adenylyl Cyclase/cAMP Pathway and CaReviews of physiology, biochemistry and pharmacology · 2021
    Review
  13. The Role of Epac in Cancer Progression.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Article
  16. Review
  17. Pharmacological modulation of the COPharmacology & therapeutics · 2018
    Review
  18. Article
  19. Functional Significance of the Adcy10-Dependent Intracellular cAMP Compartments.Journal of cardiovascular development and disease · 2018
    Review
  20. 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

9 authors at 2 institutions in 2 countries.

Jan-Paul FlackeDepartment of Clinical Pharmacology, Ruhr University Bochum, 44801 Bochum, Germany.
Hanna Flacke
Avinash Appukuttan
Rein-Jüri Palisaar
Joachim Noldus
Brian D Robinson
H Peter Reusch
Jonathan H Zippin
Yury Ladilov
Ruhr University Bochum · DECornell University · US

Funding

cAMP signaling in melanoma pathogenesis: Evidence for multiple microdomains playiK08CA160657 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZIPPIN, JONATHAN HALE · 2011 to 2015
$856k
NCI NIH HHS K08 CA160657
6 · The paper itself

Abstract

cAMP signaling plays an essential role in modulating the proliferation of different cell types, including cancer cells. Until now, the regulation of this pathway was restricted to the transmembrane class of adenylyl cyclases. In this study, significant overexpression of soluble adenylyl cyclase (sAC), an alternative source of cAMP, was found in human prostate carcinoma, and therefore, the contribution of this cyclase was investigated in the prostate carcinoma cell lines LNCaP and PC3. Suppression of sAC activity by treatment with the sAC-specific inhibitor KH7 or by sAC-specific knockdown mediated by siRNA or shRNA transfection prevented the proliferation of prostate carcinoma cells, led to lactate dehydrogenase release, and induced apoptosis. Cell cycle analysis revealed a significant rise in the G(2) phase population 12 h after sAC inhibition, which was accompanied by the down-regulation of cyclin B(1) and CDK1. sAC-dependent regulation of proliferation involves the EPAC/Rap1/B-Raf signaling pathway. In contrast, protein kinase A does not play a role. In conclusion, this study suggests a novel sAC-dependent signaling pathway that controls the proliferation of prostate carcinoma cells.

Indexed as

Adenylyl Cyclase InhibitorsAdenylyl CyclasesCell Cycle ProteinsCell DeathCell Line, TumorCell ProliferationCyclic AMPCyclic AMP-Dependent Protein KinasesG2 Phase Cell Cycle CheckpointsGene Knockdown TechniquesGuanine Nucleotide Exchange FactorsHumansImmunohistochemistryMaleMitosisProstatic NeoplasmsADCY10 protein, humanAdenylyl Cyclase InhibitorsAdenylyl CyclasesCell Cycle ProteinsCyclic AMPCyclic AMP-Dependent Protein KinasesGuanine Nucleotide Exchange FactorsRAPGEF3 protein, human

Identifiers

PMID23255611
PMCPMC3561535
OpenAlexW1997025766

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.