Evidence map›Paper›PMID 30974805›Full record

ArticleCancers2019

Ethanol-Mediated Stress Promotes Autophagic Survival and Aggressiveness of Colon Cancer Cells via Activation of Nrf2/HO-1 Pathway.

Cesare Cernigliaro, Antonella D'Anneo, Daniela Carlisi, Michela Giuliano, Antonella Marino Gammazza, Rosario Barone, Lucia Longhitano, Francesco Cappello, Sonia Emanuele, Alfio Distefano and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Nrf2 as a novel diagnostic biomarker for papillary thyroid carcinoma.European journal of histochemistry : EJH · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Bio-Waste Products ofAntioxidants (Basel, Switzerland) · 2022
    Article
  15. Identification of Small Airway Epithelium-Related Hub Genes in Chronic Obstructive Pulmonary Disease.International journal of chronic obstructive pulmonary disease · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
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

13 authors at 3 institutions in 1 country.

Cesare CernigliaroDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Biochemistry, University of Palermo, 90127 Palermo, Italy. cesare.cernigliaro@unipa.it.ORCID 0000-0002-0264-4921
Antonella D'AnneoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), Laboratory of Biochemistry, University of Palermo, 90127 Palermo, Italy. antonella.danneo@unipa.it.ORCID 0000-0002-1785-8236
Daniela CarlisiDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Biochemistry, University of Palermo, 90127 Palermo, Italy. daniela.carlisi@unipa.it.
Michela GiulianoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), Laboratory of Biochemistry, University of Palermo, 90127 Palermo, Italy. michela.giuliano@unipa.it.ORCID 0000-0002-5114-6267
Antonella Marino GammazzaDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Human Anatomy, University of Palermo, 90127 Palermo, Italy. antonella.marino@hotmail.it.
Rosario BaroneDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Human Anatomy, University of Palermo, 90127 Palermo, Italy. rosario.barone@unipa.it.
Lucia LonghitanoDepartment of Biomedical and Biotechnological Sciences, University of Catania, I-95123 Catania, Italy. lucia.longhitano@unict.it.
Francesco CappelloDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Human Anatomy, University of Palermo, 90127 Palermo, Italy. francapp@hotmail.com.ORCID 0000-0001-9288-1148
Sonia EmanueleDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Biochemistry, University of Palermo, 90127 Palermo, Italy. sonia.emanuele@unipa.it.
Alfio DistefanoDepartment of Biomedical and Biotechnological Sciences, University of Catania, I-95123 Catania, Italy. distalfio@gmail.com.
Claudia CampanellaDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Human Anatomy, University of Palermo, 90127 Palermo, Italy. claudiettacam@hotmail.com.
Giuseppe CalvarusoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), Laboratory of Biochemistry, University of Palermo, 90127 Palermo, Italy. giuseppe.calvaruso@unipa.it.
Marianna LauricellaDepartment of Biomedicine, Neurosciences and Advanced Diagnostics (BIND), Institute of Biochemistry, University of Palermo, 90127 Palermo, Italy. marianna.lauricella@unipa.it.ORCID 0000-0002-0157-3834
University of Palermo · ITIstituto Euro Mediterraneo di Scienza e Tecnologia · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidemiological studies suggest that chronic alcohol consumption is a lifestyle risk factor strongly associated with colorectal cancer development and progression. The aim of the present study was to examine the effect of ethanol (EtOH) on survival and progression of three different colon cancer cell lines (HCT116, HT29, and Caco-2). Our data showed that EtOH induces oxidative and endoplasmic reticulum (ER) stress, as demonstrated by reactive oxygen species (ROS) and ER stress markers Grp78, ATF6, PERK and, CHOP increase. Moreover, EtOH triggers an autophagic response which is accompanied by the upregulation of beclin, LC3-II, ATG7, and p62 proteins. The addition of the antioxidant N-acetylcysteine significantly prevents autophagy, suggesting that autophagy is triggered by oxidative stress as a prosurvival response. EtOH treatment also upregulates the antioxidant enzymes SOD, catalase, and heme oxygenase (HO-1) and promotes the nuclear translocation of both Nrf2 and HO-1. Interestingly, EtOH also upregulates the levels of matrix metalloproteases (MMP2 and MMP9) and VEGF. Nrf2 silencing or preventing HO-1 nuclear translocation by the protease inhibitor E64d abrogates the EtOH-induced increase in the antioxidant enzyme levels as well as the migration markers. Taken together, our results suggest that EtOH mediates both the activation of Nrf2 and HO-1 to sustain colon cancer cell survival, thus leading to the acquisition of a more aggressive phenotype.

Indexed as

autophagycolon cancer cellsER stressethanolHO-1MMPsNrf2

Identifiers

PMID30974805
PMCPMC6521343
OpenAlexW2936110085

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.