Evidence map›Paper›PMID 35683288›Full record

ArticleMaterials (Basel, Switzerland)2022

Impact of Polyrhodanine Manganese Ferrite Binary Nanohybrids (PRHD@MnFe

Krzysztof Marycz, Anna Kowalczuk, Eliza Turlej, Emilia Zachanowicz, Anna Tomaszewska, Magdalena Kulpa-Greszta, Martyna Kępska, Zofia Steczkiewicz, Robert Pązik

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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 5 institutions in 1 country.

Krzysztof MaryczDepartment of Experimental Biology, Wroclaw University of Environmental and Life Science, Norwida 27, 50-375 Wroclaw, Poland.
Anna KowalczukNational Medicines Institute (NIL), Chelmska 30/34, 00-725 Warszawa, Poland.
Eliza TurlejDepartment of Experimental Biology, Wroclaw University of Environmental and Life Science, Norwida 27, 50-375 Wroclaw, Poland.
Emilia ZachanowiczPolymer Engineering and Technology Division, Wroclaw University of Technology, Wyspianskiego 27, 50-370 Wroclaw, Poland.ORCID 0000-0003-3195-6307
Anna TomaszewskaDepartment of Biotechnology, Institute of Biology and Biotechnology, College of Natural Sciences, University of Rzeszow, Pigonia 1, 35-310 Rzeszow, Poland.ORCID 0000-0003-2548-0568
Magdalena Kulpa-GresztaDepartment of Biotechnology, Institute of Biology and Biotechnology, College of Natural Sciences, University of Rzeszow, Pigonia 1, 35-310 Rzeszow, Poland.
Martyna KępskaDepartment of Experimental Biology, Wroclaw University of Environmental and Life Science, Norwida 27, 50-375 Wroclaw, Poland.
Zofia SteczkiewiczDepartment of Experimental Biology, Wroclaw University of Environmental and Life Science, Norwida 27, 50-375 Wroclaw, Poland.
Robert PązikDepartment of Biotechnology, Institute of Biology and Biotechnology, College of Natural Sciences, University of Rzeszow, Pigonia 1, 35-310 Rzeszow, Poland.ORCID 0000-0002-4662-6688
Wrocław University of Environmental and Life Sciences · PLUniversity of Rzeszów · PLNarodowy Instytut Leków · PLRzeszów University of Technology · PLWrocław University of Science and Technology · PL

Funding

National Science Center Harmonia 9 2017/26/M/NZ5/0114
6 · The paper itself

Abstract

Osteoporosis is characterized by the reduction of bone mineral density and the weakness of the bone strength leading to fractures. Searching for new compounds that stimulate bone activity and their ability to reconstruct seems to be a promising tool in osteoporosis treatment. Here, we performed analyses comparing the impact of polyrhodanine (PRHD) and its derivatives on the viability (anti-proliferative tests), morphology and mitochondrial network (confocal microscopy) towards pre-osteoblasts (MC3T3-E1 cell line) and osteoclasts (4B12 cell line). Moreover, we assessed the expression of genes associated with the apoptosis, inflammation and osteogenic differentiation by qPCR technique. Our results clearly demonstrated that PRHD and its modification at ratio 10/90 significantly improves the pre-osteoblast's proliferative abilities, while reducing osteoclast function. The observed effects were strongly correlated with the cytoskeleton and mitochondrial network development and arrangement. Additionally, the expression profile of genes revealed enhanced apoptosis of osteoclasts in the case of PRHD and its modification at ratio 10/90. Moreover, in this case we also observed strong anti-inflammatory properties demonstrated by decreased expression of

Indexed as

apoptosisbinary nanohybridsbone remodeling markersinflammationosteoblasts/osteoclastsosteoporosispolyrhodanine manganese ferrite

Identifiers

PMID35683288
PMCPMC9181943
OpenAlexW4281735701

What OpenQuestion holds

Textmetadata
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.