Evidence map›Paper›PMID 30814897›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2018

Evaluation of antiproliferative and protective effects of Eupatorium cannabinum L. extracts.

Alice Grigore, Georgeta Neagu, Nicoleta Dobre, Adrian Albulescu, Lucian Ionita, Carmen Ionita, Radu Albulescu

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Wild-Grown RomanianPolymers · 2025
    Article
  3. 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.

Alice GrigoreDepartment of Pharmaceutical Biotechnologies, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Georgeta NeaguDepartment of Pharmacology, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Nicoleta DobreDepartment of Analytics, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Adrian AlbulescuDepartment of Pharmacology, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
Lucian IonitaDepartment of Internal Medicine, Faculty of Veterinary Medicine, University of Agronomic Sciences and Veterinary Medicine of Bucharest , Bucharest , Romania.
Carmen IonitaDepartment of Internal Medicine, Faculty of Veterinary Medicine, University of Agronomic Sciences and Veterinary Medicine of Bucharest , Bucharest , Romania.
Radu AlbulescuDepartment of Pharmacology, National Institute of Chemical-Pharmaceutical Research and Development (ICCF) , Bucharest , Romania.
National Institute For Chemical Pharmaceutical Research and Development · ROUniversity of Agronomic Sciences and Veterinary Medicine of Bucharest · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eupatorium cannabinum L. (Asteraceae) has been used for a long time for medicinal purposes due to its various pharmacological effects and richness in active compounds such as phenolics, sesquiterpenes, pyrrolizidine alkaloids, and polysaccharides. Despite the high content of compounds that have important roles in medicinal plants, there are still limited literature data regarding this valuable species. The plant was fractioned using chloroform (EC) and distilled water (EA) and HPLC analysis revealed the presence of eupatorin, eupatilin, and quercetin in EC and caefic acid and rutin in EA. The antiproliferative potential on BT-20, HepG2, Caco-2, and Jurkat cancer cell lines was assessed by MTS test. Jurkat cells were more sensitive to both extracts (IC50 of 7.35 ± 0.35 for EC and 13.77 ± 2.16 µg/mL for EA), while the other lines were susceptible only to EC (IC50 88.27 ± 1.34 on Caco-2 cells and over 100 µg/mL on BT20 and HepG2 cells) after 24 h of exposure. In an LPS-induced damage mouse model of endotoxemia, we showed that preventive administration increases the survival times of mice and leads to inhibition of proinflammatory cytokines. Both polar and nonpolar compounds are involved in exerting these effects, but further analytical studies are needed to identify the key responsible compounds and their biochemical pathways.

Indexed as

antiinflammatoryendotoxemiaHemp-agrimonymethoxyflavones

Identifiers

PMID30814897
PMCPMC6353279
OpenAlexW2887036025

What OpenQuestion holds

Textmetadata
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.