Evidence map›Paper›PMID 29951164›Full record

ArticleOxidative medicine and cellular longevity2018

Serum 8-Oxo-dG as a Predictor of Sensitivity and Outcome of Radiotherapy and Chemotherapy of Upper Gastrointestinal Tumours.

Ali Pour Khavari, Yongping Liu, Ellen He, Sven Skog, Siamak Haghdoost

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  9. Hadrontherapy Interactions in Molecular and Cellular Biology.International journal of molecular sciences · 2019
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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 2 institutions in 3 countries.

Ali Pour KhavariDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Svante Arrhenius vag 20C, 10691 Stockholm, Sweden.ORCID 0000-0003-2570-4875
Yongping LiuClinical Oncology Laboratory, Department of Oncology, Changzhou Tumour Hospital Affiliated to Suzhou University, Honghe Road No. 68, Xinbei Area, Changzhou 213032, China.ORCID 0000-0003-3755-6849
Ellen HeSino-Swed Molecular Bio-Medicine Research Institute, Shenzhen, China.
Sven SkogSino-Swed Molecular Bio-Medicine Research Institute, Shenzhen, China.
Siamak HaghdoostDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Svante Arrhenius vag 20C, 10691 Stockholm, Sweden.
Molecular Medicine Research Institute · USStockholm University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The level of oxidative stress is important in the initiation and progression of various age-related diseases, such as cancer. The level of oxidative stress may also play a significant role in cancer patients' response to treatment. We aimed to investigate whether serum 8-oxo-dG as a marker of oxidative stress is a predictor of tumour response. We used modified ELISA with a two-step filtration to analyse 8-oxo-dG in serum. The relationship between 8-oxo-dG levels, tumour response, and toxicity was studied in 19 oesophageal cancer patients who received radiotherapy and 16 gastric cancer patients who received chemotherapy. In the radiotherapy and the merged radio- and chemotherapy groups, the baseline levels of 8-oxo-dG were significantly lower in responder patients than in nonresponder patients and the increments after treatment were greater. In comparison with patients whose serum 8-oxo-dG levels decrease after treatment, patients with increasing levels had a longer median "progression-free survival." Our results, although preliminary, suggest that serum levels of 8-oxo-dG may potentially be used to predict the sensitivity and outcome of radiotherapy and chemotherapy of upper gastrointestinal tumours. Patients with 8-oxo-dG levels that are low prior to treatment and subsequently increase after treatment may be more likely to benefit from the therapy.

Indexed as

8-Hydroxy-2'-DeoxyguanosineBiomarkersDeoxyguanosineDisease ProgressionFemaleGastrointestinal NeoplasmsHumansMaleTreatment Outcome8-Hydroxy-2'-DeoxyguanosineBiomarkersDeoxyguanosine

Identifiers

PMID29951164
PMCPMC5989165
OpenAlexW2804015492

What OpenQuestion holds

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LicenceCC BY
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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.