Evidence map›Paper›PMID 28770020›Full record

ReviewOxidative medicine and cellular longevity2017

Oxidative Stress Gene Expression Profile Correlates with Cancer Patient Poor Prognosis: Identification of Crucial Pathways Might Select Novel Therapeutic Approaches.

Alessandra Leone, Maria Serena Roca, Chiara Ciardiello, Susan Costantini, Alfredo Budillon

Open access · hybridAbstract readReview
In one paragraph

Review 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 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 135 citations in OpenAlex.

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  13. TM4SF19 controls GABP-dependentProceedings of the National Academy of Sciences of the United States of America · 2024
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  15. Three-Dimensional Gene Regulation Network in Glioblastoma Ferroptosis.International journal of molecular sciences · 2023
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3 more citing papers are in PubMed but not listed here.

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.

Alessandra LeoneExperimental Pharmacology Unit, Istituto Nazionale Tumori Fondazione G. Pascale-IRCCS, Naples, Italy.ORCID 0000-0002-1051-2937
Maria Serena RocaExperimental Pharmacology Unit, Istituto Nazionale Tumori Fondazione G. Pascale-IRCCS, Naples, Italy.
Chiara CiardielloExperimental Pharmacology Unit, Istituto Nazionale Tumori Fondazione G. Pascale-IRCCS, Naples, Italy.
Susan CostantiniExperimental Pharmacology Unit, Istituto Nazionale Tumori Fondazione G. Pascale-IRCCS, Naples, Italy.
Alfredo BudillonExperimental Pharmacology Unit, Istituto Nazionale Tumori Fondazione G. Pascale-IRCCS, Naples, Italy.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of altered redox status and high reactive oxygen species (ROS) is still controversial in cancer development and progression. Intracellular levels of ROS are elevated in cancer cells suggesting a role in cancer initiation and progression; on the contrary, ROS elevated levels may induce programmed cell death and have been associated with cancer suppression. Thus, it is crucial to consider the double-face of ROS, for novel therapeutic strategies targeting redox regulatory mechanisms. In this review, in order to derive cancer-type specific oxidative stress genes' profile and their potential prognostic role, we integrated a publicly available oxidative stress gene signature with patient survival data from the Cancer Genome Atlas database. Overall, we found several genes statistically significant associated with poor prognosis in the examined six tumor types. Among them, FoxM1 and thioredoxin reductase1 expression showed the same pattern in four out of six cancers, suggesting their specific critical role in cancer-related oxidative stress adaptation. Our analysis also unveiled an enriched cellular network, highlighting specific pathways, in which many genes are strictly correlated. Finally, we discussed novel findings on the correlation between oxidative stress and cancer stem cells in order to define those pathways to be prioritized in drug development.

Indexed as

Databases, Nucleic AcidGene Expression ProfilingGene Expression Regulation, NeoplasticNeoplasmsOxidative StressForkhead Box Protein M1HumansNeoplasm ProteinsNeoplastic Stem CellsPrognosisThioredoxin Reductase 1Forkhead Box Protein M1FOXM1 protein, humanNeoplasm ProteinsThioredoxin Reductase 1TXNRD1 protein, human

Identifiers

PMID28770020
PMCPMC5523271
OpenAlexW2729768021

What OpenQuestion holds

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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.