Evidence map›Paper›PMID 29844673›Full record

ArticleInternational journal of nanomedicine2018

Mechanisms of oxidative stress, apoptosis, and autophagy involved in graphene oxide nanomaterial anti-osteosarcoma effect.

Zhibing Tang, Lin Zhao, Zaixing Yang, Zhaohui Liu, Jia Gu, Bing Bai, Jinlian Liu, Jiaying Xu, Huilin Yang

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.9field-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

32 citing papers in PubMed, 94 citations in OpenAlex.

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  18. Cytotoxicity Effect of Iron Oxide (FeFrontiers in chemistry · 2022
    Article
  19. Carboxymethylation ofOxidative medicine and cellular longevity · 2022
    Article
  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

9 authors at 3 institutions in 1 country.

Zhibing Tang *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, China.
Lin Zhao *Department of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, China.
Zaixing YangInstitute of Quantitative Biology and Medicine, SRMP and RAD-X, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, China.
Zhaohui LiuDepartment of Anatomy and Histology and Embryology, Basic Medical and Biological Sciences, School of Medicine, Soochow University, Suzhou, China.
Jia GuInstitute of Quantitative Biology and Medicine, SRMP and RAD-X, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, China.
Bing BaiInstitute of Quantitative Biology and Medicine, SRMP and RAD-X, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, China.
Jinlian LiuDepartment of Orthopaedic Surgery, Suzhou Kowloon Hospital, Shanghai Jiaotong University School of Medicine, Suzhou, China.
Jiaying XuInstitute of Quantitative Biology and Medicine, SRMP and RAD-X, Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, China.
Huilin YangDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, China.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CNSuzhou Kowloon Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGraphene and its derivative graphene oxide (GO) have been implicated in a wide range of anticancer effects. PURPOSE: The objective of this study was to systematically evaluate the toxicity and underlying mechanisms of GO on two osteosarcoma (OSA) cancer cell lines, MG-63 and K

methodsMG-63 and K

resultsK

conclusionThis paper proposes various underlying mechanisms of the anticancer effect of GO. The novel synthetic use of GO with an oxidizing agent is the key step for further potential applications in clinical OSA cancer therapy.

Indexed as

AnimalsAntineoplastic AgentsApoptosisApoptosis Regulatory ProteinsAutophagosomesAutophagyBone NeoplasmsCaspase 3Cell Line, TumorCell SurvivalGraphiteHumansMiceNanostructuresOsteosarcomaOxidative StressAntineoplastic AgentsApoptosis Regulatory ProteinsCASP3 protein, humanCaspase 3GraphiteOxidesReactive Oxygen Speciesapoptosisautophagygraphene oxideosteosarcoma cancerROS

Identifiers

PMID29844673
PMCPMC5961647
OpenAlexW2804860155

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.