Evidence map›Paper›PMID 19833720›Full record

ReviewThe Journal of endocrinology2010

The emerging role of Krüppel-like factors in endocrine-responsive cancers of female reproductive tissues.

R C M Simmen, J M P Pabona, M C Velarde, C Simmons, O Rahal, F A Simmen

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of endocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Observational
  12. Article
  13. HypermethylatedOncoTargets and therapy · 2019
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Downregulation of Kruppel-like factor 2 is associated with poor prognosis for nonsmall-cell lung cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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

6 authors at 3 institutions in 1 country.

R C M SimmenDepartment of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72202, USA. simmenrosalia@uams.edu
J M P Pabona
M C Velarde
C Simmons
O Rahal
F A Simmen
University of Arkansas for Medical Sciences · USArkansas Children's Nutrition Center · USBuck Institute for Research on Aging · US

Funding

UTEROFERRIN GENE EXPRESSION DURING DEVELOPMENTR01HD021961 · NICHD · UNIVERSITY OF FLORIDA · PI SIMMEN, ROSALIA C · 1991 to 2008
$2.1M
UTEROFERRIN GENE EXPRESSION DURING DEVELOPMENTR29HD021961 · NICHD · UNIVERSITY OF FLORIDA · PI SIMMEN, ROSALIA C · 1986 to 1990
–
NICHD NIH HHS HD21961NICHD NIH HHS R01 HD021961
6 · The paper itself

Abstract

Krüppel-like factors (KLFs), of which there are currently 17 known protein members, belong to the specificity protein (Sp) family of transcription factors and are characterized by the presence of Cys(2)/His(2) zinc finger motifs in their carboxy-terminal domains that confer preferential binding to GC/GT-rich sequences in gene promoter and enhancer regions. While previously regarded to simply function as silencers of Sp1 transactivity, many KLFs are now shown to be relevant to human cancers by their newly identified abilities to mediate crosstalk with signaling pathways involved in the control of cell proliferation, apoptosis, migration, and differentiation. Several KLFs act as tumor suppressors and/or oncogenes under distinct cellular contexts, underscoring their prognostic potential for cancer survival and outcome. Recent studies suggest that a number of KLFs can influence steroid hormone signaling through transcriptional networks involving steroid hormone receptors and members of the nuclear receptor family of transcription factors. Since inappropriate sensitivity or resistance to steroid hormone actions underlies endocrine-related malignancies, we consider the intriguing possibility that dysregulation of expression and/or activity of KLF members is linked to the pathogenesis of endometrial and breast cancers. In this review, we focus on recently described mechanisms of actions of several KLFs (KLF4, KLF5, KLF6, and KLF9) in cancers of the mammary gland and uterus. We suggest that understanding the mode of actions of KLFs and their functional networks may lead to the development of novel therapeutics to improve current prospects for cancer prevention and cure.

Indexed as

AnimalsBreast NeoplasmsFemaleHormonesHumansKruppel-Like Factor 4Kruppel-Like Transcription FactorsSignal TransductionUterine NeoplasmsHormonesKLF4 protein, humanKruppel-Like Factor 4Kruppel-Like Transcription Factors

Identifiers

PMID19833720
PMCPMC2971688
OpenAlexW2124545654

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.