Evidence map›Paper›PMID 31480430›Full record

ArticleInternational journal of molecular sciences2019

Identifying Methylation Pattern and Genes Associated with Breast Cancer Subtypes.

Lei Chen, Tao Zeng, Xiaoyong Pan, Yu-Hang Zhang, Tao Huang, Yu-Dong Cai

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

6 authors.

Lei ChenSchool of Life Sciences, Shanghai University, Shanghai 200444, China.ORCID 0000-0003-3068-1583
Tao ZengKey Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0002-0295-3994
Xiaoyong PanInstitute of Image Processing and Pattern Recognition, Shanghai Jiao Tong University, and Key Laboratory of System Control and Information Processing, Ministry of Education of China, Shanghai 200240, China.
Yu-Hang ZhangShanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Tao HuangShanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China. tohuangtao@126.com.ORCID 0000-0003-1975-9693
Yu-Dong CaiSchool of Life Sciences, Shanghai University, Shanghai 200444, China. cai_yud@126.com.ORCID 0000-0001-5664-7979

Funding

fund of the key Laboratory of Stem Cell Biology of Chinese Academy of Sciences 201703National Key R&D Program of China 2018YFC0910403National Natural Science Foundation of China 31701151Natural Science Foundation of Shanghai 17ZR1412500Science and Technology Commission of Shanghai Municipality 18dz2271000Shanghai Municipal Science and Technology Major Project 2017SHZDZX01Shanghai Sailing Program 16YF1413800Youth Innovation Promotion Association of the Chinese Academy of Sciences 2016245
6 · The paper itself

Abstract

Breast cancer is regarded worldwide as a severe human disease. Various genetic variations, including hereditary and somatic mutations, contribute to the initiation and progression of this disease. The diagnostic parameters of breast cancer are not limited to the conventional protein content and can include newly discovered genetic variants and even genetic modification patterns such as methylation and microRNA. In addition, breast cancer detection extends to detailed breast cancer stratifications to provide subtype-specific indications for further personalized treatment. One genome-wide expression-methylation quantitative trait loci analysis confirmed that different breast cancer subtypes have various methylation patterns. However, recognizing clinically applied (methylation) biomarkers is difficult due to the large number of differentially methylated genes. In this study, we attempted to re-screen a small group of functional biomarkers for the identification and distinction of different breast cancer subtypes with advanced machine learning methods. The findings may contribute to biomarker identification for different breast cancer subtypes and provide a new perspective for differential pathogenesis in breast cancer subtypes.

Indexed as

DNA MethylationBreast NeoplasmsEpigenesis, GeneticFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMachine LearningQuantitative Trait Locibreast cancermethylationmulti-class classificationpatternsubtype

Identifiers

PMID31480430
PMCPMC6747348

What Socratic 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 Socratic graph.