Evidence map›Paper›PMID 31742371›Full record

ArticleTurkish journal of medical sciences2020

Carvacrol alters soluble factors in HCT-116 and HT-29 cell lines

Ahu Pakdemirli, Caner Karaca, Tolga Sever, Ezgi Daşkin, Asim Leblebici, Türkan Yiğitbaşi, Yasemin Başbinar

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  9. Antioxidants (Basel, Switzerland) · 2022
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Phytochemistry and Pharmacology ofEvidence-based complementary and alternative medicine : eCAM · 2021
    Review
  15. 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

7 authors at 2 institutions in 1 country.

Ahu PakdemirliDepartment of First and Emergency Aid, Vocational School of Health Services, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0001-9224-3007
Caner KaracaDepartment of Basic Oncology, Institute of Health Sciences, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0002-9016-3908
Tolga SeverDepartment of Translational Oncology, Institute of Health Sciences, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0002-0135-0243
Ezgi DaşkinDepartment of Translational Oncology, Institute of Health Sciences, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0001-6542-2608
Asim LeblebiciDepartment of Translational Oncology, Institute of Health Sciences, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0002-5197-6631
Türkan YiğitbaşiDepartment of Biochemistry, Faculty of Medicine, İstanbul Medipol University, İstanbul, TurkeyORCID 0000-00020675-1839
Yasemin BaşbinarDepartment of Translational Oncology, Institute of Oncology, Dokuz Eylül University, İzmir, TurkeyORCID 0000-0001-9439-2217
Dokuz Eylül University · TRIstanbul Medipol University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: Natural products are popular insights for researchers to investigate promising anti-cancer agents since some of these substances have lesser adverse effects restricting the treatment than traditional chemotherapeutic agents. A well-known monoterpene Carvacrol, widely consumed in Mediterranean cuisine and lower risks of cancer, has efficient anticancer effects. However, the mechanism of action is yet to be discovered. Materials and methods: The investigation aims to illuminate a new perceptive in the role of this substance on colorectal cancer treatment, by the means of differences in a well-defined range of soluble factors. Carvacrol effect on both HT-29 and HCT-116 cell lines was evaluated on proliferation and the IC50 values were calculated by the RTCA xCELLigence device. Then MAGPIX assay was performed to obtain the changes in soluble factors of the cell lines. Results: The Multiplexing assay suggests some of these factors were altered in favor of surviving and proliferation in aggressive cell line HCT-116 whereas they were altered against these characters in HT-29, were correlated with the increased IC50 concentration of HCT- 116 in carvacrol treatment. Conclusion: The current study indicates that differences in the levels of these soluble factors could modulate the anticancer effect related to carvacrol.

Indexed as

Cell ProliferationColorectal NeoplasmsCymenesGranulocyte-Macrophage Colony-Stimulating FactorHCT116 CellsHT29 CellsHumansLeptinProlactinTransforming Growth Factor alphaVascular Endothelial Growth Factor Receptor-2carvacrolCymenesGranulocyte-Macrophage Colony-Stimulating FactorKDR protein, humanLeptinProlactinTransforming Growth Factor alphaVascular Endothelial Growth Factor Receptor-2Carvacrolcolon cancerphytochemicalsoluble factors

Identifiers

PMID31742371
PMCPMC7080355
OpenAlexW3012571511

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.