Evidence map›Paper›PMID 32699215›Full record

Observational studyNature communications2020

Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma.

Wei Cao, Hayan Lee, Wei Wu, Aubhishek Zaman, Sean McCorkle, Ming Yan, Justin Chen, Qinghe Xing, Nasa Sinnott-Armstrong, Hongen Xu and 20 more

3 registry-linked trialsAbstract readObservational Study
In one paragraph

Observational study in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing 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.

NCT05680077 completednot on this mapstarted 2022, after this paper: background citation

Methylation Detection of KCNA3 and OTOP2 Genes in Plasma for the Auxiliary Diagnosis of Esophageal Cancer/Precancerous Lesions: a Clinical Trial

Typeobservational_patient_registrySponsorWuhan Ammunition Life-tech Co., LtdRan2022 to 2023Enrolled1,116ConditionsEsophageal NeoplasmsArmsKCNA3 and OTOP2 Gene Methylation Combined Detection Kit (Fluorescent PCR Method)
NCT06476067 recruitingnot on this map

Predicting Postoperative Early Tumor Recurrence in Patients With Esophageal Squamous Cell Carcinoma

TypeobservationalSponsorCity of Hope Medical CenterRan2006 to 2028Enrolled150ConditionsEsophageal Cancer, Recurrence, DNA MethylationArmsSurgery
NCT06490003 recruitingnot on this map

Predicting Postoperative Chemotherapy Efficacy in Patients With Esophageal Squamous Cell Carcinoma by Biopsy Specimens.

TypeobservationalSponsorCity of Hope Medical CenterRan2004 to 2028Enrolled150ConditionsEsophageal Squamous Cell Carcinoma, Chemotherapy Effect, DNA MethylationArmsFluoro Uracil
3 · Its place in the literature

Who cites it

82 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Esophageal cancer: from pathogenesis to precision therapies.Signal transduction and targeted therapy · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

22 more citing papers are in PubMed but not listed here.

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

30 authors.

Wei Cao *Translational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China. caowei7@zzu.edu.cn.ORCID http://orcid.org/0000-0002-2851-4359
Hayan Lee *Department of Genetics, School of Medicine, Stanford University, CA, USA.ORCID http://orcid.org/0000-0003-0571-3192
Wei Wu *Department of Medicine, University of California San Francisco, San Francisco, CA, USA. wei.wu@ucsf.edu.ORCID http://orcid.org/0000-0002-6556-067X
Aubhishek Zaman *Department of Medicine, University of California San Francisco, San Francisco, CA, USA.
Sean McCorkleComputational Science Initiative, Brookhaven National Laboratory, Upton, NY, USA.
Ming YanBasic Medical College, Zhengzhou University, Zhengzhou, China.
Justin ChenDepartment of Genetics, School of Medicine, Stanford University, CA, USA.
Qinghe XingInstitutes of Biomedical Sciences and Children's Hospital, Fudan University, Shanghai, China.
Nasa Sinnott-ArmstrongDepartment of Genetics, School of Medicine, Stanford University, CA, USA.ORCID http://orcid.org/0000-0003-4490-0601
Hongen XuPrecision Medicine Center, The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
M Reza SailaniDepartment of Genetics, School of Medicine, Stanford University, CA, USA.
Wenxue TangPrecision Medicine Center, The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
Yuanbo CuiTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Jia LiuTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Hongyan GuanTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Pengju LvTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Xiaoyan SunTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Lei SunTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Pengli HanTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Yanan LouTranslational Medical Center, Zhengzhou Central Hospital Affiliated Zhengzhou University, Zhengzhou, China.
Jing ChangJiangsu Mai Jian Biotechnology Development Company, Wuxi, China.
Jinwu WangDepartment of Pathology, Linzhou Cancer Hospital, Linzhou, China.
Yuchi GaoAnnoroad Gene Company, Beijing, China.
Jiancheng GuoPrecision Medicine Center, The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
Gundolf SchenkBakar Computational Health Sciences Institute, University of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-1240-9949
Alan Hunter ShainDepartment of Dermatology, University of California San Francisco, San Francisco, CA, USA.
Fred G BiddleDepartment of Biological Sciences, University of Calgary, Calgary, Canada.
Eric CollissonDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Michael SnyderDepartment of Genetics, School of Medicine, Stanford University, CA, USA. mpsnyder@stanford.edu.ORCID http://orcid.org/0000-0003-0784-7987
Trever G BivonaDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA. trever.bivona@ucsf.edu.ORCID http://orcid.org/0000-0001-5734-4128

Funding

UCSF Project 1U54CA224081 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Collin M Blakely · 2017 to 2026
$12.9M
Molecular and Cellular Mechanisms in CancerT32CA108462 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOGA, ANDREI · 2004 to 2024
$10.4M
The Cancer Target Discovery and Development Network at UCSFU01CA217882 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BANDYOPADHYAY, SOURAV, BIVONA, TREVER G · 2017 to 2021
$5.2M
Visualization hub for genomics data exploration and translational discoveryU24CA210974 · NCI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI COLLISSON, ERIC, HAUSSLER, DAVID H · 2016 to 2020
$4.2M
Characterization of YAP as a rational companion target in lung cancerR01CA204302 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Trever G Bivona · 2017 to 2026
$3.7M
Rational Combined Inhibition of NF-kB and EGFR to Optimize Lung Cancer TreatmentR01CA169338 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BIVONA, TREVER G · 2013 to 2023
$3.4M
Genomics and Functional Characterization of NF1-mutated Lung CancerR01CA227807 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2018 to 2022
$2.8M
The structural and functional basis of MET exon 14 activation and acquired drug resistanceR01CA230263 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC, JURA, NATALIA · 2019 to 2023
$2.0M
Optimizing Treatment Approaches to Lung Cancers Harboring MET Exon 14 mutationsR01CA239604 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2019 to 2023
$2.0M
Optimizing biologically-based rational polytherapy in ALK+ lung cancerR01CA211052 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BIVONA, TREVER G · 2017 to 2021
$1.8M
Tailoring Therapy to Pancreatic Cancer SubtypesR01CA222862 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2018 to 2022
$1.8M
Crucial Microenvironmental Cofactors for Pancreatic Cancer PathogenesisR01CA178015 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLISSON, ERIC · 2014 to 2018
$1.5M
NCI NIH HHS K22 CA217997NCI NIH HHS R01 CA169338NCI NIH HHS R01 CA178015NCI NIH HHS R01 CA204302NCI NIH HHS R01 CA211052NCI NIH HHS R01 CA222862NCI NIH HHS R01 CA227807NCI NIH HHS R01 CA230263NCI NIH HHS R01 CA239604NCI NIH HHS T32 CA108462NCI NIH HHS U01 CA217882NCI NIH HHS U24 CA210974NCI NIH HHS U54 CA224081NIH HHS S10 OD020141
6 · The paper itself

Abstract

Epigenetic landscapes can shape physiologic and disease phenotypes. We used integrative, high resolution multi-omics methods to delineate the methylome landscape and characterize the oncogenic drivers of esophageal squamous cell carcinoma (ESCC). We found 98% of CpGs are hypomethylated across the ESCC genome. Hypo-methylated regions are enriched in areas with heterochromatin binding markers (H3K9me3, H3K27me3), while hyper-methylated regions are enriched in polycomb repressive complex (EZH2/SUZ12) recognizing regions. Altered methylation in promoters, enhancers, and gene bodies, as well as in polycomb repressive complex occupancy and CTCF binding sites are associated with cancer-specific gene dysregulation. Epigenetic-mediated activation of non-canonical WNT/β-catenin/MMP signaling and a YY1/lncRNA ESCCAL-1/ribosomal protein network are uncovered and validated as potential novel ESCC driver alterations. This study advances our understanding of how epigenetic landscapes shape cancer pathogenesis and provides a resource for biomarker and target discovery.

Indexed as

Epigenesis, GeneticGene Expression Regulation, NeoplasticAgedBiomarkers, TumorCell Line, TumorChromatin Immunoprecipitation SequencingCohort StudiesCpG IslandsDatasets as TopicDNA MethylationEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaEsophagectomyEsophagusFemaleGenomicsBiomarkers, TumorHeterochromatinHistones

Identifiers

PMID32699215
PMCPMC7376194

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.