Evidence map›Paper›PMID 37110792›Full record

ArticleMolecules (Basel, Switzerland)2023

Systematic Studies on Anti-Cancer Evaluation of Stilbene and Dibenzo[

Filip Borys, Piotr Tobiasz, Marcin Poterała, Hanna Fabczak, Hanna Krawczyk, Ewa Joachimiak

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Synthesis and Study of Building Blocks with Dibenzo[International journal of molecular sciences · 2024
    Article
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

6 authors at 2 institutions in 1 country.

Filip BorysDepartment of Organic Chemistry, Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland.ORCID 0000-0002-1029-540X
Piotr TobiaszDepartment of Organic Chemistry, Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland.
Marcin PoterałaDepartment of Organic Chemistry, Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland.ORCID 0000-0003-0283-3148
Hanna FabczakNencki Institute of Experimental Biology, Polish Academy of Sciences, 02-093 Warsaw, Poland.
Hanna KrawczykDepartment of Organic Chemistry, Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland.
Ewa JoachimiakNencki Institute of Experimental Biology, Polish Academy of Sciences, 02-093 Warsaw, Poland.ORCID 0000-0003-3185-7923
Warsaw University of Technology · PLInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

budget funds for science in the years 2019-2023 Diamond Grant projectNational Science Center OPUS15 2018/29/B/NZ3/02443Operational Project Knowledge Education Development 2014-2020 co-financed by the European Social Fund POWR.03.02.00-00-I007/16-00 (POWER 2014-2020)Warsaw University of Technology Research University (IDUB) program (NChem 3)
6 · The paper itself

Abstract

Cancer is one of the most common causes of human death worldwide; thus, numerous therapies, including chemotherapy, have been and are being continuously developed. In cancer cells, an aberrant mitotic spindle-a microtubule-based structure necessary for the equal splitting of genetic material between daughter cells-leads to genetic instability, one of the hallmarks of cancer. Thus, the building block of microtubules, tubulin, which is a heterodimer formed from α- and β-tubulin proteins, is a useful target in anti-cancer research. The surface of tubulin forms several pockets, i.e., sites that can bind factors that affect microtubules' stability. Colchicine pockets accommodate agents that induce microtubule depolymerization and, in contrast to factors that bind to other tubulin pockets, overcome multi-drug resistance. Therefore, colchicine-pocket-binding agents are of interest as anti-cancer drugs. Among the various colchicine-site-binding compounds, stilbenoids and their derivatives have been extensively studied. Herein, we report systematic studies on the antiproliferative activity of selected stilbenes and oxepine derivatives against two cancer cell lines-HCT116 and MCF-7-and two normal cell lines-HEK293 and HDF-A. The results of molecular modeling, antiproliferative activity, and immunofluorescence analyses revealed that compounds

Indexed as

Antineoplastic AgentsNeoplasmsStilbenesBinding SitesCell ProliferationColchicineHEK293 CellsHumansMicrotubulesOxepinsTubulinTubulin ModulatorsAntineoplastic AgentsColchicineOxepinsStilbenesTubulinTubulin Modulatorsbiological activitycancer cellcolchicine-binding sitedibenzo[b,f]oxepinemicrotubuletubulin

Identifiers

PMID37110792
PMCPMC10146957
OpenAlexW4366426212

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.