Evidence map›Paper›PMID 25794149›Full record

ArticlePloS one2015

Heat-modified citrus pectin induces apoptosis-like cell death and autophagy in HepG2 and A549 cancer cells.

Lionel Leclere, Maude Fransolet, Francois Cote, Pierre Cambier, Thierry Arnould, Pierre Van Cutsem, Carine Michiels

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 67 citations in OpenAlex.

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  17. The Role of Nonerythroid SpectrinJournal of oncology · 2019
    Review
  18. Review
  19. Article
  20. Bicalutamide enhances fodrin-mediated apoptosis through calpain in LNCaP.Experimental biology and medicine (Maywood, N.J.) · 2018
    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 1 institution in 1 country.

Lionel LeclereLaboratory of Biochemistry and Cellular Biology-URBC, NARILIS, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Maude FransoletLaboratory of Biochemistry and Cellular Biology-URBC, NARILIS, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Francois CoteLaboratory of Biochemistry and Cellular Biology-URBC, NARILIS, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Pierre CambierLaboratory of Plant Cellular Biology-URBV, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Thierry ArnouldLaboratory of Biochemistry and Cellular Biology-URBC, NARILIS, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Pierre Van CutsemLaboratory of Plant Cellular Biology-URBV, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
Carine MichielsLaboratory of Biochemistry and Cellular Biology-URBC, NARILIS, University of Namur, 61 rue de Bruxelles, 5000, Namur, Belgium.
University of Namur · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is still one of the leading causes of death worldwide, and finding new treatments remains a major challenge. Previous studies showed that modified forms of pectin, a complex polysaccharide present in the primary plant cell wall, possess anticancer properties. Nevertheless, the mechanism of action of modified pectin and the pathways involved are unclear. Here, we show that citrus pectin modified by heat treatment induced cell death in HepG2 and A549 cells. The induced cell death differs from classical apoptosis because no DNA cleavage was observed. In addition, Z-VAD-fmk, a pan-caspase inhibitor, did not influence the observed cell death in HepG2 cells but appeared to be partly protective in A549 cells, indicating that heat-modified citrus pectin might induce caspase-independent cell death. An increase in the abundance of the phosphatidylethanolamine-conjugated Light Chain 3 (LC3) protein and a decrease in p62 protein abundance were observed in both cell types when incubated in the presence of heat-modified citrus pectin. These results indicate the activation of autophagy. To our knowledge, this is the first time that autophagy has been revealed in cells incubated in the presence of a modified form of pectin. This autophagy activation appears to be protective, at least for A549 cells, because its inhibition with 3-methyladenine increased the observed modified pectin-induced cytotoxicity. This study confirms the potential of modified pectin to improve chemotherapeutic cancer treatments.

Indexed as

Hot TemperatureAdenineApoptosisAutophagyCarrier ProteinsCaspase InhibitorsCaspasesCell Line, TumorHep G2 CellsHumansMacrolidesMicrofilament ProteinsPectinsSpectrinUbiquitination3-methyladenineAdeninebafilomycin ACarrier ProteinsCaspase InhibitorsCaspasescitrus pectinMacrolidesMicrofilament ProteinsPectinsSpectrin

Identifiers

PMID25794149
PMCPMC4368604
OpenAlexW2040641992

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.