Evidence map›Paper›PMID 34641401›Full record

ArticleMolecules (Basel, Switzerland)2021

Epithelial-to-Mesenchymal Transition Is Not a Major Modulating Factor in the Cytotoxic Response to Natural Products in Cancer Cell Lines.

Baris Kucukkaraduman, Ekin Gokce Cicek, Muhammad Waqas Akbar, Secil Demirkol Canli, Burcak Vural, Ali Osmay Gure

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 43% 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

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

  1. Pooled it
  2. 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

6 authors at 4 institutions in 1 country.

Baris KucukkaradumanDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.ORCID 0000-0002-5475-281X
Ekin Gokce CicekDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Muhammad Waqas AkbarDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Secil Demirkol CanliMolecular Pathology Application and Research Center, Hacettepe University, Ankara 06100, Turkey.ORCID 0000-0003-0200-7962
Burcak VuralDepartment of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Turkey.
Ali Osmay GureDepartment of Medical Biology, Acibadem University, Istanbul 34684, Turkey.ORCID 0000-0002-4064-8608
Bilkent University · TRAcıbadem University · TRHacettepe University · TRIstanbul University · TR

Funding

Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi ONAP 46784Türkiye Bilimsel ve Teknolojik Araştirma Kurumu BIDEB-2211-E
6 · The paper itself

Abstract

Numerous natural products exhibit antiproliferative activity against cancer cells by modulating various biological pathways. In this study, we investigated the potential use of eight natural compounds (apigenin, curcumin, epigallocatechin gallate, fisetin, forskolin, procyanidin B2, resveratrol, urolithin A) and two repurposed agents (fulvestrant and metformin) as chemotherapy enhancers and mesenchymal-to-epithelial (MET) inducers of cancer cells. Screening of these compounds in various colon, breast, and pancreatic cancer cell lines revealed anti-cancer activity for all compounds, with curcumin being the most effective among these in all cell lines. Although some of the natural products were able to induce MET in some cancer cell lines, the MET induction was not related to increased synergy with either 5-FU, irinotecan, gemcitabine, or gefitinib. When synergy was observed, for example with curcumin and irinotecan, this was unrelated to MET induction, as assessed by changes in E-cadherin and vimentin expression. Our results show that MET induction is compound and cell line specific, and that MET is not necessarily related to enhanced chemosensitivity.

Indexed as

Drug SynergismEpithelial-Mesenchymal TransitionAntineoplastic AgentsBiological ProductsBiomarkers, TumorBreast NeoplasmsCell MovementCell ProliferationColonic NeoplasmsFemaleHumansPancreatic NeoplasmsAntineoplastic AgentsBiological ProductsBiomarkers, Tumorcancerchemotherapy resistanceepithelial-to-mesenchymal transitionmesenchymal-to-epithelial transitionnatural products

Identifiers

PMID34641401
PMCPMC8512490
OpenAlexW3204590340

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.