Evidence map›Paper›PMID 22628407›Full record

ArticleCancer discovery2012

miR-23a promotes the transition from indolent to invasive colorectal cancer.

Sohail Jahid, Jian Sun, Robert A Edwards, Diana Dizon, Nicole C Panarelli, Jeffrey W Milsom, Shaheen S Sikandar, Zeynep H Gümüs, Steven M Lipkin

Abstract read
In one paragraph

Article in Cancer discovery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% 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

89 citing papers in PubMed, 2 syntheses or guidelines pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Extracellular vesicles in colorectal cancer.Annals of coloproctology · 2025
    Review
  6. Article
  7. Article
  8. MTSS1: beyond the integration of actin and membrane dynamics.Cellular and molecular life sciences : CMLS · 2024
    Review
  9. Molecular insights and clinical implications for the tumor suppressor role of SCFBiochimica et biophysica acta. Reviews on cancer · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Sohail JahidDepartments of Medicine, Genetic Medicine, Surgery, Pathology and Physiology and Biophysics, Weill Cornell Medical College, New York, New York 10021, USA.
Jian Sun
Robert A Edwards
Diana Dizon
Nicole C Panarelli
Jeffrey W Milsom
Shaheen S Sikandar
Zeynep H Gümüs
Steven M Lipkin
Cornell University · USCalifornia Institute for Regenerative Medicine · USStanford University · USUniversity of California, Irvine · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
DNA Mismatch Repair and associated genes in suppression of GI adenomas and carcinR01CA098626 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIPKIN, STEVEN M · 2004 to 2014
$2.9M
Multi-scale modeling of asymmetric cell divisionR01GM095990 · NIGMS · CORNELL UNIVERSITY · PI SHEN, XILING · 2011 to 2015
$1.5M
Mechanisms of Notch Signalling in Colon Cancer Initiating CellsR21CA153049 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LIPKIN, STEVEN M · 2010 to 2011
$398k
NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA098626NCI NIH HHS R21 CA153049NIGMS NIH HHS R01 GM095990NIGMS NIH HHS R01GM095990
6 · The paper itself

Abstract

Colorectal cancer is a classic example of a tumor that progresses through multiple distinct stages in its evolution. To understand the mechanisms regulating the transition from indolent to invasive disease, we profiled somatic copy number alterations in noninvasive adenomas and invasive adenocarcinomas from Apc and DNA mismatch repair (MMR) mutant mouse models. We identified a recurrent amplicon on mouse chromosome 8 that encodes microRNA (miRNA) 23a and -27a (miR). miR-23a and -27a levels are upregulated in mouse intestinal adenocarcinomas, primary tumors from patients with stage I/II colorectal cancers, as well as in human colorectal cancer cell lines and cancer stem cells. Functionally, miR-23a promotes the migration and invasion of colorectal cancer cells and stem cells, whereas miR-27a primarily promotes proliferation. We computationally and experimentally validated that metastasis suppressor 1 (MTSS1) is a direct miR-23a target and similarly validated that the ubiquitin ligase FBXW7 is a direct miR-27a target. Analyses of computationally predicted target genes in microarray data sets of patients with colorectal cancers are consistent with a role for miR-23a, but not miR-27a, specifically in invasive colorectal cancers.

Indexed as

AdenocarcinomaAdenomaAnimalsColorectal NeoplasmsDNA Copy Number VariationsF-Box ProteinsF-Box-WD Repeat-Containing Protein 7HumansMiceMice, Inbred C57BLMice, TransgenicMicroRNAsNeoplasm InvasivenessProto-Oncogene Proteins c-junProto-Oncogene Proteins c-mycUbiquitin-Protein LigasesF-Box ProteinsF-Box-WD Repeat-Containing Protein 7Fbxw7 protein, mouseMicroRNAsMirn23b microRNA, mouseMirn27 microRNA, mouseMyc protein, mouseProto-Oncogene Proteins c-junProto-Oncogene Proteins c-mycUbiquitin-Protein Ligases

Identifiers

PMID22628407
PMCPMC3651884
OpenAlexW2128775512

What OpenQuestion holds

Textmetadata
LicenceTDM
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.