Evidence map›Paper›PMID 33065997›Full record

ArticleInternational journal of molecular sciences2020

TMPE Derived from Saffron Natural Monoterpene as Cytotoxic and Multidrug Resistance Reversing Agent in Colon Cancer Cells.

Kamila Środa-Pomianek, Anna Palko-Łabuz, Andrzej Poła, Mirosława Ferens-Sieczkowska, Olga Wesołowska, Agata Kozioł

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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, 8 citations in OpenAlex.

  1. Review
  2. 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 1 institution in 1 country.

Kamila Środa-PomianekDepartment of Biophysics and Neurobiology, Wroclaw Medical University, ul. Chalubinskiego 3, 50-368 Wroclaw, Poland.ORCID 0000-0003-3454-5044
Anna Palko-ŁabuzDepartment of Biophysics and Neurobiology, Wroclaw Medical University, ul. Chalubinskiego 3, 50-368 Wroclaw, Poland.ORCID 0000-0002-4246-5717
Andrzej PołaDepartment of Biophysics and Neurobiology, Wroclaw Medical University, ul. Chalubinskiego 3, 50-368 Wroclaw, Poland.
Mirosława Ferens-SieczkowskaDepartment of Chemistry and Immunochemistry, Wroclaw Medical University, ul. M. Skłodowskiej-Curie 48/50, 50-369 Wrocław, Poland.
Olga WesołowskaDepartment of Biophysics and Neurobiology, Wroclaw Medical University, ul. Chalubinskiego 3, 50-368 Wroclaw, Poland.ORCID 0000-0003-1659-3288
Agata KoziołDepartment of Chemistry and Immunochemistry, Wroclaw Medical University, ul. M. Skłodowskiej-Curie 48/50, 50-369 Wrocław, Poland.
Wroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Terpenes constitute one of the largest groups of natural products. They exhibit a wide range of biological activities including antioxidant, anticancer, and drug resistance modulating properties. Saffron extract and its terpene constituents have been demonstrated to be cytotoxic against various types of cancer cells, including breast, liver, lung, pancreatic, and colorectal cancer. In the present work, we have studied anticancer properties of TMPE, a newly synthesized monoterpene derivative of β-cyclocitral-the main volatile produced by the stigmas of unripe crocuses. TMPE presented selective cytotoxic activity to doxorubicin-resistant colon cancer cells and was identified to be an effective MDR modulator in doxorubicin-resistant cancer cells. Synergy between this derivative and doxorubicin was observed. Most probably, TMPE inhibited transport activity of ABCB1 protein without affecting its expression level. Analysis of TMPE physicochemical parameters suggested it was not likely to be transported by ABCB1. Molecular modeling showed TMPE being more reactive molecule than the parental compound-β-cyclocitral. Analysis of electrostatic potential maps of both compounds prompted us to hypothesize that reduced reactivity as well as susceptibility to electrophilic attack were related to the lower general toxicity of β-cyclocitral. All of the above pointed to TMPE as an interesting candidate molecule for MDR reversal in cancer cells.

Indexed as

Antineoplastic AgentsDrug Resistance, NeoplasmOrganic ChemicalsAldehydesATP Binding Cassette Transporter, Subfamily B, Member 1Binding SitesCell ProliferationColonic NeoplasmsCrocusCyclohexenesDiterpenesHT29 CellsHumansProtein BindingAldehydesAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1beta-cyclocitralCyclohexenesDiterpenesOrganic ChemicalsTPME monoterpene derivativeABCB1 transporter (P-glycoprotein)anticancer activitycolon cancermonoterpenemultidrug resistance (MDR) reversalsaffronβ-cyclocitral

Identifiers

PMID33065997
PMCPMC7589963
OpenAlexW3093157643

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.