Evidence map›Paper›PMID 29163752›Full record

ArticleOxidative medicine and cellular longevity2017

Cytotoxicity, Oxidative Stress, Cell Cycle Arrest, and Mitochondrial Apoptosis after Combined Treatment of Hepatocarcinoma Cells with Maleic Anhydride Derivatives and Quercetin.

Gabriela Carrasco-Torres, Rafael Baltiérrez-Hoyos, Erik Andrade-Jorge, Saúl Villa-Treviño, José Guadalupe Trujillo-Ferrara, Verónica Rocío Vásquez-Garzón

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
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  19. Effective Cellular Transport ofInternational journal of molecular sciences · 2020
    Article
  20. Targeting Kinases inFrontiers in veterinary science · 2020
    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 2 institutions in 1 country.

Gabriela Carrasco-TorresDepartamento de Bioquímica y Sección de Graduados, Escuela Superior de Medicina del IPN, Ciudad de México, Mexico.ORCID 0000-0002-1127-0095
Rafael Baltiérrez-HoyosCONACYT, Facultad de Medicina y Cirugía, Universidad Autónoma Benito Juárez de Oaxaca, Oaxaca de Juárez, OAX, Mexico.
Erik Andrade-JorgeDepartamento de Bioquímica y Sección de Graduados, Escuela Superior de Medicina del IPN, Ciudad de México, Mexico.
Saúl Villa-TreviñoDepartamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de México, Mexico.
José Guadalupe Trujillo-FerraraDepartamento de Bioquímica y Sección de Graduados, Escuela Superior de Medicina del IPN, Ciudad de México, Mexico.ORCID 0000-0002-1979-6489
Verónica Rocío Vásquez-GarzónCONACYT, Facultad de Medicina y Cirugía, Universidad Autónoma Benito Juárez de Oaxaca, Oaxaca de Juárez, OAX, Mexico.ORCID 0000-0002-4861-8235
Instituto Politécnico Nacional · MXBenito Juárez Autonomous University of Oaxaca · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inflammatory condition of malignant tumors continually exposes cancer cells to reactive oxygen species, an oxidizing condition that leads to the activation of the antioxidant defense system. A similar activation occurs with glutathione production. This oxidant condition enables tumor cells to maintain the energy required for growth, proliferation, and evasion of cell death. The objective of the present study was to determine the effect on hepatocellular carcinoma cells of a combination treatment with maleic anhydride derivatives (prooxidants) and quercetin (an antioxidant). The results show that the combination of a prooxidant/antioxidant had a cytotoxic effect on HuH7 and HepG2 liver cancer cells, but not on either of two normal human epithelial cell lines or on primary hepatocytes. The combination treatment triggered apoptosis in hepatocellular carcinoma cells by activating the intrinsic pathway and causing S phase arrest during cell cycle progression. There is also clear evidence of a modification in cytoskeletal actin and nucleus morphology at 24 and 48 h posttreatment. Thus, the current data suggest that the combination of two anticarcinogenic drugs, a prooxidant followed by an antioxidant, can be further explored for antitumor potential as a new treatment strategy.

Indexed as

ApoptosisCarcinoma, HepatocellularCell Cycle CheckpointsLiver NeoplasmsMaleic AnhydridesMitochondriaOxidative StressQuercetinMaleic AnhydridesQuercetin

Identifiers

PMID29163752
PMCPMC5661749
OpenAlexW2762354243

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.