Evidence map›Paper›PMID 25273507›Full record

ArticleJournal of cancer research and clinical oncology2015

ZNF695 methylation predicts a response of esophageal squamous cell carcinoma to definitive chemoradiotherapy.

Takamasa Takahashi, Satoshi Yamahsita, Yasunori Matsuda, Takayoshi Kishino, Takeshi Nakajima, Ryoji Kushima, Ken Kato, Hiroyasu Igaki, Yuji Tachimori, Harushi Osugi and 2 more

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Article in Journal of cancer research and clinical oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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

13 citing papers in PubMed.

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  5. Article
  6. Role of Epigenetics for the Efficacy of Cisplatin.International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

12 authors.

Takamasa TakahashiDivision of Epigenomics, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Satoshi Yamahsita
Yasunori Matsuda
Takayoshi Kishino
Takeshi Nakajima
Ryoji Kushima
Ken Kato
Hiroyasu Igaki
Yuji Tachimori
Harushi Osugi
Masato Nagino
Toshikazu Ushijima

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDefinitive chemoradiotherapy (dCRT) is one of the standard treatments for esophageal squamous cell carcinoma. Patients with a response to dCRT have a better prognosis than those resistant to dCRT while survival benefits for patients with residual tumors are limited. Nevertheless, few molecular markers to predict the response to dCRT are currently available. Here, we aimed to establish a DNA methylation marker to predict the response to dCRT.

methodsA total of 104 patients were divided into screening (n = 43) and validation (n = 61) sets. A genome-wide DNA methylation analysis was performed using an Infinium HumanMethylation450 BeadChip array. Methylation levels were measured by quantitative methylation-specific PCR and normalized by the fraction of cancer cells in a sample.

resultsThe genome-wide methylation analysis of seven responders and eight non-responders identified 18 genomic regions specifically (un)methylated in the responders. Among these, methylation of the promoter CpG island of ZNF695 was significantly associated with the response to dCRT in the screening set (P = 0.004), and a cutoff value was determined. In the validation set, the association was successfully validated (P = 0.021), and a high specificity (90 %) for the prediction of responders was obtained using the prefixed cutoff value. In addition, a multivariate analysis showed that ZNF695 methylation was an independent predictive factor for the response to dCRT (OR 7.55, 95 % CI 2.12-26.9, P = 0.002).

conclusionZNF695 methylation was significantly associated with the response to dCRT and is a promising predictive marker for the response to dCRT.

Indexed as

ChemoradiotherapyDNA MethylationAdenocarcinomaAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Squamous CellCase-Control StudiesCisplatinDNA-Binding ProteinsEsophageal NeoplasmsFemaleFluorouracilFollow-Up StudiesHumansMaleBiomarkers, TumorCisplatinDNA-Binding ProteinsFluorouracil

Identifiers

PMID25273507
PMCPMC11824055

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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.