Evidence map›Paper›PMID 30302280›Full record

ArticleCell death discovery2018

Selective toxicity of tumor treating fields to melanoma: an in vitro and in vivo study.

Yunhui Jo, Sang-Gu Hwang, Yeung Bae Jin, Jiwon Sung, Youn Kyoung Jeong, Jeong Hwa Baek, Jae-Min Cho, Eun Ho Kim, Myonggeun Yoon

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  19. Frontiers in oncology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yunhui Jo1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Sang-Gu Hwang1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Yeung Bae Jin3National Primate Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141 Republic of Korea.
Jiwon Sung2Department of Bio-Convergence Engineering, Korea University, Seoul, 02842 Republic of Korea.
Youn Kyoung Jeong4Radiation Non-Clinical Center, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Jeong Hwa Baek1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Jae-Min Cho1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Eun Ho Kim *1Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, 01812 Republic of Korea.
Myonggeun Yoon *2Department of Bio-Convergence Engineering, Korea University, Seoul, 02842 Republic of Korea.
Korea Institute of Radiological and Medical Sciences · KRKorea University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor treating fields (TTFs) are a newly developed cancer therapy technology using an alternating electric field that may be a possible candidate for overcoming the limitations of conventional treatment methods currently used in cancer treatment. Although clinical results using TTFs appear promising, concerns regarding side effects must be clarified to demonstrate the effectiveness of this treatment method. To investigate the side effects of TTF treatment, the damage to normal cell lines and normal tissue of a mouse model was compared with the damage to tumor cells and tumors in a mouse model after TTF treatment. No serious damage was found in the normal cells and normal tissues of the mouse model, suggesting that the side effects of TTF treatment may not be serious. Our evidence based on in vitro and in vivo experiments suggests that TTF may cause selective damage to cancer cells, further demonstrating the potential of TTF as an attractive alternative to conventional cancer treatment modalities.

Identifiers

PMID30302280
PMCPMC6170382
OpenAlexW2894570671

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.