Evidence map›Paper›PMID 30361641›Full record

ArticleScientific reports2018

Angiotensin 1-7 modulates molecular and cellular processes central to the pathogenesis of prostate cancer.

Kamila Domińska, Piotr Okła, Karolina Kowalska, Dominika Ewa Habrowska-Górczyńska, Kinga Anna Urbanek, Tomasz Ochędalski, Agnieszka Wanda Piastowska-Ciesielska

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  11. Renin-angiotensin system and cancer: epidemiology, cell signaling, genetics and epigenetics.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

7 authors at 1 institution in 1 country.

Kamila DomińskaDepartment of Comparative Endocrinology, Medical University of Lodz, Lodz, 90-752, Poland. kamila.dominska@umed.lodz.pl.
Piotr OkłaDepartment of Comparative Endocrinology, Medical University of Lodz, Lodz, 90-752, Poland.
Karolina KowalskaLaboratory of Cell Cultures and Genomic Analysis, Medical University of Lodz, Lodz, 90-752, Poland.
Dominika Ewa Habrowska-GórczyńskaLaboratory of Cell Cultures and Genomic Analysis, Medical University of Lodz, Lodz, 90-752, Poland.
Kinga Anna UrbanekDepartment of Comparative Endocrinology, Medical University of Lodz, Lodz, 90-752, Poland.
Tomasz OchędalskiDepartment of Comparative Endocrinology, Medical University of Lodz, Lodz, 90-752, Poland.
Agnieszka Wanda Piastowska-CiesielskaDepartment of Comparative Endocrinology, Medical University of Lodz, Lodz, 90-752, Poland.
Medical University of Lodz · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiotensin 1-7 (Ang1-7) is an endogenous bioactive component of the renin-angiotensin system (RAS). In addition to its cardiovascular properties, its anti-proliferative and anti-angiogenic traits are believed to play important roles in carcinogenesis. The present study examines the influence of Ang1-7 on processes associated with development and progression of prostate cancer cells. Our findings indicate that while Ang1-7 (1 nM; 48 h) can effectively reduce cell proliferation in DU-145, it can induce a significant decrease in the expression of MKI67 in LNCaP. In both cell lines we also observed a reduction in colony size in soft agar assay. A various changes in gene expression were noted after exposure to Ang1-7: those of anti- and pro-apoptotic agents and the NF-kB family of transcription factors, as well as mesenchymal cell markers and vascular endothelial growth factor A (VEGFA). In addition, Ang1-7 was found to modulate cell adhesion and matrix metallopeptidase (MMP) activity. Changes were also observed in the levels of angiotensin receptors and sex steroid hormone receptors. Ang1-7 reduced the levels of estrogen receptor alpha gene (ESR1) and increased the expression of estrogen receptor beta gene (ESR2) in all prostate cancer cells; it also up-regulated androgen receptor (AR) expression in androgen-sensitive cells but contradictory effect was observed in androgen- irresponsive cell lines. In summary, the results confirm the existence of complex network between the various elements of the local RAS and the molecular and cellular mechanisms of prostate cancerogenesis. The response of cancer cells to Ang1-7 appears to vary dependently on the dose and time of incubation as well as the aggressiveness and the hormonal status of cells.

Indexed as

Angiotensin ICell AdhesionCell CountCell CycleCell Line, TumorCell MovementCell ProliferationCell SurvivalExtracellular Matrix ProteinsGene Expression Regulation, NeoplasticHumansMaleNeoplasm InvasivenessPeptide FragmentsProstatic NeoplasmsRNA, MessengerAngiotensin Iangiotensin I (1-7)Extracellular Matrix ProteinsPeptide FragmentsRNA, Messenger

Identifiers

PMID30361641
PMCPMC6202343
OpenAlexW2897278416

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Registered trials

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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.