Evidence map›Paper›PMID 36695998›Full record

ArticleInvestigational new drugs2023

Novel pentacyclic derivatives and benzylidenes of the progesterone series cause anti-estrogenic and antiproliferative effects and induce apoptosis in breast cancer cells.

Alexander M Scherbakov, Svetlana K Vorontsova, Alvina I Khamidullina, Jasminka Mrdjanovic, Olga E Andreeva, Fedor B Bogdanov, Diana I Salnikova, Vladimir Jurisic, Igor V Zavarzin, Valerii Z Shirinian

Open access · hybridAbstract read
In one paragraph

Article in Investigational new drugs, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 29 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

10 authors at 6 institutions in 3 countries.

Alexander M Scherbakov *Department of Experimental Tumor Biology, Blokhin N.N. National Medical Research Center of Oncology, Kashirskoye shosse 24, 115522, Moscow, Russia. a.sherbakov@ronc.ru.ORCID http://orcid.org/0000-0002-2974-9555
Svetlana K Vorontsova *N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect 47, 119991, Moscow, Russia.
Alvina I KhamidullinaCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Institute of Gene Biology, Russian Academy of Sciences, Vavilov Street 34/5, 119334, Moscow, Russian Federation.ORCID http://orcid.org/0000-0001-8137-0625
Jasminka MrdjanovicOncology Institute of Vojvodina, Faculty of Medicine, University of Novi Sad, Put Dr Goldmana 4, 21204, Sremska Kamenica, Serbia.ORCID http://orcid.org/0000-0003-3486-1610
Olga E AndreevaDepartment of Experimental Tumor Biology, Blokhin N.N. National Medical Research Center of Oncology, Kashirskoye shosse 24, 115522, Moscow, Russia.ORCID http://orcid.org/0000-0002-6015-6619
Fedor B BogdanovDepartment of Experimental Tumor Biology, Blokhin N.N. National Medical Research Center of Oncology, Kashirskoye shosse 24, 115522, Moscow, Russia.ORCID http://orcid.org/0000-0002-0976-0335
Diana I SalnikovaDepartment of Experimental Tumor Biology, Blokhin N.N. National Medical Research Center of Oncology, Kashirskoye shosse 24, 115522, Moscow, Russia.ORCID http://orcid.org/0000-0002-0809-3710
Vladimir JurisicFaculty of Medical Sciences, University of Kragujevac, Svetozara Markovica 69, 34000, Kragujevac, Serbia.ORCID http://orcid.org/0000-0001-6525-128X
Igor V ZavarzinN.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect 47, 119991, Moscow, Russia.ORCID http://orcid.org/0000-0002-8194-5756
Valerii Z ShirinianN.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect 47, 119991, Moscow, Russia.ORCID http://orcid.org/0000-0001-9480-3565
N.D. Zelinsky Institute of Organic Chemistry · RURussian Cancer Research Center NN Blokhin · RUInstitute of Gene Biology · RULomonosov Moscow State University · RUUniversity of Kragujevac · RSUniversity of Novi Sad · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The promising antitumor effects of progesterone derivatives have been identified in many studies. However, the specific mechanism of action of this class of compounds has not been fully described. Therefore, in this study, we investigated the antiproliferative and (anti)estrogenic activities of novel pentacyclic derivatives and benzylidenes of the progesterone series. The antiproliferative effects of the compounds were evaluated on hormone-dependent MCF7 breast cancer cells using the MTT test. Estrogen receptor α (ERα) activity was assessed by a luciferase-based reporter assay. Immunoblotting was used to evaluate the expression of signaling proteins. All benzylidenes demonstrated inhibitory effects with IC

Indexed as

Antineoplastic AgentsBreast NeoplasmsApoptosisCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorEstrogen AntagonistsEstrogen Receptor alphaFemaleHumansProgesteroneStructure-Activity RelationshipAntineoplastic AgentsEstrogen AntagonistsEstrogen Receptor alphaProgesteroneAntiestrogenic activityBenzylidenesBreast cancerEstrogen receptor αPentacyclic steroids

Identifiers

PMID36695998
PMCPMC9875769
OpenAlexW4317936710

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.