Evidence map›Paper›PMID 16980615›Full record

ArticleMolecular and cellular biology2006

DACH1 is a cell fate determination factor that inhibits cyclin D1 and breast tumor growth.

Kongming Wu, Anping Li, Mahadev Rao, Manran Liu, Vernon Dailey, Ying Yang, Dolores Di Vizio, Chenguang Wang, Michael P Lisanti, Guido Sauter and 3 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

80 citing papers in PubMed, 133 citations in OpenAlex.

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  17. RDGN-based predictive model for the prognosis of breast cancer.Experimental hematology & oncology · 2020
    Article
  18. Skeletal muscle: A review of molecular structure and function, in health and disease.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Review
  19. Review
  20. Article

20 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

13 authors at 7 institutions in 2 countries.

Kongming WuKimmel Cancer Center, Department of Cancer Biology, Bluemle Life Sciences Building, Philadelphia, Pennsylvania 19107, USA.
Anping Li
Mahadev Rao
Manran Liu
Vernon Dailey
Ying Yang
Dolores Di Vizio
Chenguang Wang
Michael P Lisanti
Guido Sauter
Robert G Russell
Ales Cvekl
Richard G Pestell
Thomas Jefferson University · USAlbert Einstein College of Medicine · USGeorgetown University · USGeorgetown University Medical Center · USSidney Kimmel Cancer Center · USUniversity Medical Center Hamburg-Eppendorf · DEYeshiva University · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
PAX-6 AS A KEY REGULATOR OF LENS DEVELOPMENTR01EY012200 · NEI · YESHIVA UNIVERSITY · PI CVEKL, ALES · 2000 to 2025
$13.1M
Initiation and Maintenance In Mammary TumorigenesisR01CA075503 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 1998 to 2011
$4.6M
CYCLIN D1 FUNCTION IN PROSTATE CANCERR01CA086072 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 2001 to 2013
$3.3M
REGULATION OF CYCLIN D1 EXPRESSIONR01CA070896 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 2000 to 2010
$3.2M
NCI NIH HHS P30 CA056036NCI NIH HHS P30CA56036NCI NIH HHS R01 CA070896NCI NIH HHS R01 CA075503NCI NIH HHS R01 CA086072NCI NIH HHS R01CA70896NCI NIH HHS R01CA75503NCI NIH HHS R01CA86071NCI NIH HHS R01CA86072NEI NIH HHS EY12200NEI NIH HHS R01 EY012200
6 · The paper itself

Abstract

Obstacles to the expansion of cells with proliferative potential include the induction of cell death, telomere-based senescence, and the pRb and p53 tumor suppressors. Not infrequently, the molecular pathways regulating oncogenesis recapitulate aberrations of processes governing embryogenesis. The genetic network, consisting of the dachshund (dac), eyes absent (eya), eyeless, and sine oculis (so) genes, regulates cell fate determination in metazoans, with dac serving as a cointegrator through a So DNA-binding factor. Here, DACH1 inhibited oncogene-mediated breast oncogenesis, blocking breast cancer epithelial cell DNA synthesis, colony formation, growth in Matrigel, and tumor growth in mice. Genetic deletion studies demonstrated a requirement for cyclin D1 in DACH1-mediated inhibition of DNA synthesis. DACH1 repressed cyclin D1 through a novel mechanism via a c-Jun DNA-binding partner, requiring the DACH1 alpha-helical DS domain which recruits corepressors to the local chromatin. Analysis of over 2,000 patients demonstrated increased nuclear DACH1 expression correlated inversely with cellular mitosis and predicted improved breast cancer patient survival. The cell fate determination factor, DACH1, arrests breast tumor proliferation and growth in vivo providing a new mechanistic and potential therapeutic insight into this common disease.

Indexed as

AnimalsBinding SitesBreast NeoplasmsCells, CulturedCyclin D1DNAEpithelial CellsEye ProteinsFemaleHumansMammary Glands, AnimalMammary Glands, HumanMiceMice, NudeNeoplasm InvasivenessNeoplasm MetastasisCyclin D1DACH1 protein, humanDach1 protein, mouseDNAEye ProteinsProto-Oncogene Proteins c-mycras ProteinsTranscription Factor AP-1Transcription Factors

Identifiers

PMID16980615
PMCPMC1592900
OpenAlexW2114111754

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.