Evidence map›Paper›PMID 26925128›Full record

ArticleArchives of medical science : AMS2016

Estrogen receptor β promoter methylation: a potential indicator of malignant changes in breast cancer.

Lei Gao, Xiaolong Qi, Kaiwen Hu, Ruili Zhu, Wei Xu, Shipeng Sun, Lixin Zhang, Ximing Yang, Baojin Hua, Guijian Liu

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Lei GaoLaboratory Department, GuangAn'men Hospital, China Academy of Chinese Medical Sciences, Beijing, China; Department of Oncology, Beijing Hospital of Traditional Chinese Medicine, Capital University of Medical Sciences, Beijing, China.
Xiaolong QiDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Kaiwen HuDepartment of Oncology, Dongfang Hospital Affiliated to Beijing University of Chinese Medicine, Beijing, China.
Ruili ZhuLaboratory Department, GuangAn'men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Wei XuDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shipeng SunLaboratory Department, GuangAn'men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Lixin ZhangAnyang Cancer Hospital, Anyang, China.
Ximing YangLaboratory Department, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing, China.
Baojin HuaDepartment of Oncology, GuangAn'men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Guijian LiuLaboratory Department, GuangAn'men Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Guang’anmen Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNSouthern Medical University · CNAnyang Tumor Hospital · CNBeijing University of Chinese Medicine · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEstrogen receptor β (ERβ) always lacks expression in estrogen-dependent tumors, which may result from gene inactivation by methylation. In this study, we aimed to determine whether aberrant methylation of the ERβ promoter is associated with decreased ERβ gene expression in breast cancer. MATERIAL AND

methodsERβ methylation status was determined for 132 pairs of breast cancer and adjacent normal tissues via the MethyLight method. Additionally, mRNA relative expression was quantified by real-time polymerase chain reaction (RT-PCR) to determine whether aberrant methylation had a negative correlation with expression. The correlation of ERβ promoter methylation and clinical parameters is also discussed.

resultsMethylation was observed in 96 (72.7%) breast cancer samples, and the median percentage of fully methylated reference (PMR) among methylated tissues was 0.83. Meanwhile, 94 (71.2%) adjacent normal tissues were methylated and the median PMR was 0.48. Compared to adjacent normal tissues, the methylation level of breast cancer was significantly higher (p < 0.001) and mRNA expression was much lower (p < 0.001). There was a significant correlation between ERβ methylation and mRNA expression in adjacent normal breast tissues (p = 0.004). In addition, the methylation rate of cancer tissues whose maximum diameter < 3 cm was significantly higher than those > 3 cm (p = 0.025).

conclusionsERβ promoter methylation level varies between cancerous and adjacent normal breast tissues. There was significant downregulation of ERβ methylation expression in pre-cancerous stages of breast cancer. Therefore, demethylation drugs may offer a potential strategy for preventing the development of pre-cancerous cells.

Indexed as

breast cancerestrogen receptor βmethylationpercentage of fully methylated reference

Identifiers

PMID26925128
PMCPMC4754373
OpenAlexW2316543249

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.