Evidence map›Paper›PMID 28283822›Full record

ArticleEuropean journal of nutrition2018

Antiproliferative activity of vitexin-2-O-xyloside and avenanthramides on CaCo-2 and HepG2 cancer cells occurs through apoptosis induction and reduction of pro-survival mechanisms.

Emanuele Salvatore Scarpa, Elena Antonini, Francesco Palma, Michele Mari, Paolino Ninfali

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Article in European journal of nutrition, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.7field-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

17 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
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  5. Article
  6. Genes · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Overview of the Anticancer Profile of Avenanthramides from Oat.International journal of molecular sciences · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Article
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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

5 authors at 1 institution in 1 country.

Emanuele Salvatore ScarpaDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Urbino, PU, 61029, Italy.
Elena AntoniniDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Urbino, PU, 61029, Italy.
Francesco PalmaDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Urbino, PU, 61029, Italy.
Michele MariDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Urbino, PU, 61029, Italy.
Paolino NinfaliDepartment of Biomolecular Sciences, University of Urbino "Carlo Bo", Urbino, PU, 61029, Italy. paolino.ninfali@uniurb.it.ORCID http://orcid.org/0000-0003-4471-725X
University of Urbino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCaCo-2 colon cancer cells and HepG2 liver cancer cells represent two malignant cell lines, which show a high resistance to apoptosis induced by the conventional anticancer drugs. Vitexin-2-O-xyloside (XVX) and avenanthramides (AVNs) are naturally occurring dietary agents from Beta vulgaris var. cicla L. and Avena sativa L., respectively. The aim of this work was to evaluate the antiproliferative effects and the reduction of the pro-survival mechanisms exerted by XVX and AVNs, used individually and in combination, in CaCo-2 and HepG2 cancer cells.

methodsXVX and AVNs were isolated by liquid chromatography and characterized by HPLC-PDA-MS. The XVX and AVN antiproliferative effects were evaluated through sulforhodamine B method, while their pro-apoptotic effects through caspase activity assays. RTqPCR was used to investigate the modulation of the pro-survival factors baculoviral inhibitor of apoptosis repeat-containing 5 (BIRC5), hypoxia inducible factor 1 A (HIF1A), and vascular endothelial growth factor A (VEGFA). Cellular antioxidant activity (CAA) was investigated by means of DCFH-DA assay, whereas chemical antioxidant capacity was evaluated by the ORAC method.

resultsXVX and AVNs, both individually and in combination, inhibited the proliferation of CaCo-2 and HepG2 cancer cells, through activation of caspases 9, 8, and 3. XVX and AVNs downregulated the pro-survival genes BIRC5, HIF1A, and VEGFA. The CAA assay showed that AVNs exhibited strong antioxidant activity inside both CaCo-2 and HepG2 cells.

conclusionsThe antiproliferative activity of the XVX + AVNs mixture represents an innovative treatment, which is effective against two types of cancer cells characterized by high resistance to the conventional anticancer drugs.

Indexed as

ApoptosisCaco-2 CellsCell Line, TumorCell ProliferationFlavonoidsGlycosidesHumansortho-AminobenzoatesVascular Endothelial Growth Factor Aavenanthramide-2CFlavonoidsGlycosidesortho-AminobenzoatesVascular Endothelial Growth Factor Avitexin-2-O-xylosideApoptosisAvenanthramidesCaCo-2 colon cancer cellsCellular antioxidant activityHepG2 liver cancer cellsVitexin-2-O-xyloside

Identifiers

PMID28283822
OpenAlexW2592570788

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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.