Evidence map›Paper›PMID 29453410›Full record

ArticleScientific reports2018

Molecular characterization of colorectal adenomas with and without malignancy reveals distinguishing genome, transcriptome and methylome alterations.

Brooke R Druliner, Panwen Wang, Taejeong Bae, Saurabh Baheti, Seth Slettedahl, Douglas Mahoney, Nikolaos Vasmatzis, Hang Xu, Minsoo Kim, Matthew Bockol and 16 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
7.1field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Tetraspanin 6 is a regulator of carcinogenesis in colorectal cancer.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  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

26 authors at 4 institutions in 2 countries.

Brooke R DrulinerDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Panwen WangHealth Sciences Research, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Taejeong BaeBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Saurabh BahetiBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Seth SlettedahlBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Douglas MahoneyBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Nikolaos VasmatzisBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Hang XuCenter for Genomic Sciences & School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-8336-4445
Minsoo KimBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Matthew BockolInformation Technology, Mayo Clinic, Rochester, MN, 55905, USA.
Daniel O'BrienBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Diane GrillBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Nathaniel WarnerBiomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, 55905, USA.
Miguel Munoz-GomezDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Kimberlee KossickDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Ruth JohnsonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Mohamad MouchliDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Donna Felmlee-DevineDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Jill Washechek-AlettoDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Thomas SmyrkAnatomic Pathology, Mayo Clinic, Rochester, MN, 55905, USA.
Ann ObergDepartment of Health Sciences Research, Cancer Center Statistics Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0003-2539-9807
Junwen WangHealth Sciences Research, Mayo Clinic, Scottsdale, AZ, 85259, USA.
Nicholas ChiaDepartment of Health Sciences Research, Center for Individualized Medicine, College of Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Alexej AbyzovDepartment of Health Sciences Research, Center for Individualized Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
David AhlquistDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA.
Lisa A BoardmanDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, 55905, USA. boardman.lisa@mayo.edu.ORCID 0000-0002-1330-2054
Mayo Clinic in Arizona · USMayo Clinic in Florida · USMayo Clinic · USUniversity of Hong Kong · HK

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
Time lapse to cancer: defining transition from polyp to colorectal cancer (PQ14)R01CA170357 · NCI · MAYO CLINIC ROCHESTER · PI BOARDMAN, LISA ALLYN · 2012 to 2016
$2.5M
Microbial Metabolic Toxicity Drives Colon CancerR01CA179243 · NCI · MAYO CLINIC ROCHESTER · PI CHIA, NICHOLAS · 2014 to 2018
$2.0M
NCI NIH HHS R01 CA170357NCI NIH HHS R01 CA179243NIDDK NIH HHS P30 DK084567
6 · The paper itself

Abstract

The majority of colorectal cancer (CRC) arises from precursor lesions known as polyps. The molecular determinants that distinguish benign from malignant polyps remain unclear. To molecularly characterize polyps, we utilized Cancer Adjacent Polyp (CAP) and Cancer Free Polyp (CFP) patients. CAPs had tissues from the residual polyp of origin and contiguous cancer; CFPs had polyp tissues matched to CAPs based on polyp size, histology and dysplasia. To determine whether molecular features distinguish CAPs and CFPs, we conducted Whole Genome Sequencing, RNA-seq, and RRBS on over 90 tissues from 31 patients. CAPs had significantly more mutations, altered expression and hypermethylation compared to CFPs. APC was significantly mutated in both polyp groups, but mutations in TP53, FBXW7, PIK3CA, KIAA1804 and SMAD2 were exclusive to CAPs. We found significant expression changes between CAPs and CFPs in GREM1, IGF2, CTGF, and PLAU, and both expression and methylation alterations in FES and HES1. Integrative analyses revealed 124 genes with alterations in at least two platforms, and ERBB3 and E2F8 showed aberrations specific to CAPs across all platforms. These findings provide a resource of molecular distinctions between polyps with and without cancer, which have the potential to enhance the diagnosis, risk assessment and management of polyps.

Indexed as

DNA MethylationGene Expression ProfilingGenomicsAdenomaColorectal NeoplasmsHumansSequence Analysis, RNA

Identifiers

PMID29453410
PMCPMC5816667
OpenAlexW2795634164

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.