Evidence map›Paper›PMID 29290975›Full record

ArticleOncotarget2017

GPER is involved in the regulation of the estrogen-metabolizing CYP1B1 enzyme in breast cancer.

Francesca Cirillo, Michele Pellegrino, Rocco Malivindi, Vittoria Rago, Silvia Avino, Luigina Muto, Vincenza Dolce, Adele Vivacqua, Damiano Cosimo Rigiracciolo, Paola De Marco and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  8. CYP1B1 as a therapeutic target in cardio-oncology.Clinical science (London, England : 1979) · 2020
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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

15 authors at 3 institutions in 2 countries.

Francesca CirilloDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Michele PellegrinoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Rocco MalivindiDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Vittoria RagoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Silvia AvinoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Luigina MutoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Vincenza DolceDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Adele VivacquaDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Damiano Cosimo RigiraccioloDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Paola De MarcoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Anna SebastianiDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Sergio AbonanteRegional Hospital Cosenza, Cosenza, Italy.
Miki NakajimaFaculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan.
Rosamaria LappanoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Marcello MaggioliniDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
University of Calabria · ITAzienda Ospedaliera di Cosenza · ITKanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cytochrome P450 1B1 (CYP1B1) is a heme-thiolate monooxygenase involved in both estrogen biosynthesis and metabolism. For instance, CYP1B1 catalyzes the hydroxylation of E2 leading to the production of 4-hydroxyestradiol that may act as a potent carcinogenic agent. In addition, CYP1B1 is overexpressed in different tumors including breast cancer. In this scenario, it is worth mentioning that CYP1B1 expression is triggered by estrogens through the estrogen receptor (ER)α in breast cancer cells. In the present study, we evaluated whether the G protein estrogen receptor namely GPER may provide an alternate route toward the expression and function of CYP1B1 in ER-negative breast cancer cells, in main players of the tumor microenvironment as cancer associated fibroblasts (CAFs) that were obtained from breast cancer patients, in CAFs derived from a cutaneous metastasis of an invasive mammary ductal carcinoma and in breast tumor xenografts. Our results show that GPER along with the EGFR/ERK/c-Fos transduction pathway can lead to CYP1B1 regulation through the involvement of a half-ERE sequence located within the CYP1B1 promoter region. As a biological counterpart, we found that both GPER and CYP1B1 mediate growth effects

Indexed as

breast cancercancer-associated fibroblastsCYP1B1estrogenGPER

Identifiers

PMID29290975
PMCPMC5739760
OpenAlexW2770341483

What OpenQuestion holds

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LicenceCC BY
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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.