Evidence map›Paper›PMID 27811934›Full record

ReviewExperimental & molecular medicine2016

ROS homeostasis and metabolism: a critical liaison for cancer therapy.

Jongdoo Kim, Jaehong Kim, Jong-Sup Bae

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 291 citations in OpenAlex.

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67 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

3 authors at 2 institutions in 1 country.

Jongdoo KimCancer Control Team, Gachon University Gil Medical Center, Incheon, Republic of Korea.
Jaehong KimDepartment of Biochemistry, School of Medicine, Gachon University, Incheon, Republic of Korea.
Jong-Sup BaeCollege of Pharmacy, CMRI, Research Institute of Pharmaceutical Sciences, Daegu, Republic of Korea.
Gachon University · KRGachon University Gil Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence indicates that hypoxia and oxidative stress can control metabolic reprogramming of cancer cells and other cells in tumor microenvironments and that the reprogrammed metabolic pathways in cancer tissue can also alter the redox balance. Thus, important steps toward developing novel cancer therapy approaches would be to identify and modulate critical biochemical nodes that are deregulated in cancer metabolism and determine if the therapeutic efficiency can be influenced by changes in redox homeostasis in cancer tissues. In this review, we will explore the molecular mechanisms responsible for the metabolic reprogramming of tumor microenvironments, the functional modulation of which may disrupt the effects of or may be disrupted by redox homeostasis modulating cancer therapy.

Indexed as

Molecular Targeted TherapyOxidative StressAnimalsAntineoplastic AgentsGlucoseHomeostasisHumansMetabolic Networks and PathwaysNeoplasmsOxidation-ReductionReactive Oxygen SpeciesTumor MicroenvironmentAntineoplastic AgentsGlucoseReactive Oxygen Species

Identifiers

PMID27811934
PMCPMC5133371
OpenAlexW2546719732

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.