Evidence map›Paper›PMID 27374083›Full record

ArticleOncotarget2016

The activation of OR51E1 causes growth suppression of human prostate cancer cells.

Désirée Maßberg, Nikolina Jovancevic, Anne Offermann, Annika Simon, Aria Baniahmad, Sven Perner, Thanakorn Pungsrinont, Katarina Luko, Stathis Philippou, Burkhard Ubrig and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 67 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 4 institutions in 1 country.

Désirée MaßbergDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Nikolina JovancevicDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Anne OffermannPathology of the University Hospital of Luebeck and the Leibniz Research Center Borstel, Luebeck and Borstel, Germany.
Annika SimonDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Aria BaniahmadInstitute of Human Genetics, Jena University Hospital, Jena, Germany.
Sven PernerPathology of the University Hospital of Luebeck and the Leibniz Research Center Borstel, Luebeck and Borstel, Germany.
Thanakorn PungsrinontInstitute of Human Genetics, Jena University Hospital, Jena, Germany.
Katarina LukoInstitute of Human Genetics, Jena University Hospital, Jena, Germany.
Stathis PhilippouInstitute for Pathology und Cytology, Augusta-Kranken-Anstalt gGmbH Bochum, Bochum, Germany.
Burkhard UbrigClinic for Urology, Augusta-Kranken-Anstalt gGmbH Bochum, Bochum, Germany.
Markus HeilandClinic for Urology, Augusta-Kranken-Anstalt gGmbH Bochum, Bochum, Germany.
Lea WeberDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Janine AltmüllerCologne Center for Genomics, University of Köln, Köln, Germany.
Christian BeckerCologne Center for Genomics, University of Köln, Köln, Germany.
Günter GisselmannDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Lian GelisDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Hanns HattDepartment of Cell Physiology, Ruhr-University Bochum, Bochum, Germany.
Ruhr University Bochum · DEAugusta-Kranken-Anstalt · DEJena University Hospital · DEResearch Center Borstel - Leibniz Lung Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of prostate cancer (PCa) is regulated by the androgen-dependent activity of the androgen receptor (AR). Androgen-deprivation therapy (ADT) is therefore the gold standard treatment to suppress malignant progression of PCa. Nevertheless, due to the development of castration resistance, recurrence of disease after initial response to ADT is a major obstacle to successful treatment. As G-protein coupled receptors play a fundamental role in PCa physiology, they might represent promising alternative or combinatorial targets for advanced diseases. Here, we verified gene expression of the olfactory receptors (ORs) OR51E1 [prostate-specific G-protein coupled receptor 2 (PSGR2)] and OR51E2 (PSGR) in human PCa tissue by RNA-Seq analysis and RT-PCR and elucidated the subcellular localization of both receptor proteins in human prostate tissue. The OR51E1 agonist nonanoic acid (NA) leads to the phosphorylation of various protein kinases and growth suppression of the PCa cell line LNCaP. Furthermore, treatment with NA causes reduction of androgen-mediated AR target gene expression. Interestingly, NA induces cellular senescence, which coincides with reduced E2F1 mRNA levels. In contrast, treatment with the structurally related compound 1-nonanol or the OR2AG1 agonist amyl butyrate, neither of which activates OR51E1, did not lead to reduced cell growth or an induction of cellular senescence. However, decanoic acid, another OR51E1 agonist, also induces cellular senescence. Thus, our results suggest the involvement of OR51E1 in growth processes of PCa cells and its impact on AR-mediated signaling. These findings provide novel evidences to support the functional importance of ORs in PCa pathogenesis.

Indexed as

Cell Line, TumorCell ProliferationCellular SenescenceDisease ProgressionHumansMaleNeoplasm ProteinsPhosphorylationProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantReceptors, AndrogenReceptors, G-Protein-CoupledSignal TransductionTransfectionAR protein, humanNeoplasm ProteinsOR51E1 protein, humanReceptors, AndrogenReceptors, G-Protein-Coupledandrogen receptorcellular senescenceOR51E1proliferationprostate cancer

Identifiers

PMID27374083
PMCPMC5217014
OpenAlexW2466663546

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.