Evidence map›Paper›PMID 19221491›Full record

ReviewCell cycle (Georgetown, Tex.)2009

Let-7 and miR-200 microRNAs: guardians against pluripotency and cancer progression.

Marcus E Peter

Open access · hybridAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 239 papers.

0numbers the graph read from it
0cells of the map it votes in
239citing papers in PubMed
18.5field-weighted citation impact, top 1% 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

239 citing papers in PubMed, 404 citations in OpenAlex.

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  7. Epithelial-mesenchymal transition in tissue repair and degeneration.Nature reviews. Molecular cell biology · 2024
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179 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

1 author at 1 institution in 1 country.

Marcus E PeterThe Ben May Department for Cancer Research, The University of Chicago, Chicago, Illinois 60637, USA. mpeter@uchicago.edu
University of Chicago · US

Funding

MOLECULAR CHARACTERIZATION OF THE TWO CD95 PATHWAYSR01GM061712 · NIGMS · UNIVERSITY OF CHICAGO · PI PETER, MARCUS E. · 2000 to 2007
$2.1M
NIGMS NIH HHS R01 GM061712NIGMS NIH HHS R01 GM61712
6 · The paper itself

Abstract

Micro (mi)RNAs are emerging as important regulators of cellular differentiation, their importance underscored by the fact that they are often dysregulated during carcinogenesis. Two evolutionary conserved families, let-7 and miR-200, regulate key differentiation processes during development. Loss of let-7 in cancer results in reverse embryogenesis and dedifferentiation, and miR-200 has been identified as a powerful regulator of epithelial-to-mesenchymal transition (EMT). Recent findings have connected let-7 with stem cell maintenance and point at a connection between EMT and stem cell formation. A part of tumor progression can be viewed as a continuum of progressive dedifferentiation (EMT) with a cell at the endpoint that has stem cell-like properties. I propose that steps of this process are driven by specific changes in the expression of let-7 and miR-200 family members.

Indexed as

AnimalsCell DifferentiationHumansMiceMicroRNAsNeoplasmsNeoplastic Stem CellsPluripotent Stem CellsSignal TransductionTranscription FactorsMicroRNAsMIRN200 microRNA, humanmirnlet7 microRNA, humanTranscription Factors

Identifiers

PMID19221491
PMCPMC2688687
OpenAlexW2059160575

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.