Evidence map›Paper›PMID 29720900›Full record

ReviewClinics in colon and rectal surgery2018

Update on Sporadic Colorectal Cancer Genetics.

Karin M Hardiman

Abstract readReview
In one paragraph

Review in Clinics in colon and rectal surgery, 2018. 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

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

13 citing papers in PubMed.

  1. Review
  2. Integrated molecular profiling ofJournal of gastrointestinal oncology · 2024
    Article
  3. Review
  4. Article
  5. Review
  6. Diagnostics (Basel, Switzerland) · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

1 author.

Karin M HardimanDivision of Colon and Rectal Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan.

Funding

Intra-tumor Heterogeneity in Colorectal Cancer Progression and Treatment ResponseK08CA190645 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HARDIMAN, KARIN MARIE · 2016 to 2019
$700k
NCI NIH HHS K08 CA190645NCI NIH HHS L30 CA189003
6 · The paper itself

Abstract

Our understanding of the genetics of colorectal cancer has changed dramatically over recent years. Colorectal cancer can be classified in multiple different ways. Along with the advent of whole-exome sequencing, we have gained an understanding of the scale of the genetic changes found in sporadic colorectal cancer. We now know that there are multiple pathways that are commonly involved in the evolution of colorectal cancer including Wnt/β-catenin, RAS, EGFR, and PIK3 kinase. Another recent leap in our understanding of colorectal cancer genetics is the recognition that many, if not all tumors, are actually genetically heterogeneous within individual tumors and also between tumors. Recent research has revealed the prognostic and possibly therapeutic implications of various specific mutations, including specific mutations in

Indexed as

colorectal cancerexome sequencinghyper-mutated tumorsintra-tumor heterogeneity

Identifiers

PMID29720900
PMCPMC5929885

What OpenQuestion holds

Textmetadata
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.