Evidence map›Paper›PMID 15741234›Full record

ArticleJournal of cell science2005

Higher-order nuclear organization in growth arrest of human mammary epithelial cells: a novel role for telomere-associated protein TIN2.

Patrick Kaminker, Cedric Plachot, Sahn-Ho Kim, Peter Chung, Danielle Crippen, Ole W Petersen, Mina J Bissell, Judith Campisi, Sophie A Lelièvre

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact, top 98% 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

28 citing papers in PubMed, 0 citations in OpenAlex.

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  15. Review
  16. Gene expression in the third dimension: the ECM-nucleus connection.Journal of mammary gland biology and neoplasia · 2010
    Review
  17. Article
  18. Review
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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

9 authors at 3 institutions in 1 country.

Patrick KaminkerBuck Institute for Age Research, 8001 Redwood Boulevard, Novato, California 94945, USA.
Cedric Plachot
Sahn-Ho Kim
Peter Chung
Danielle Crippen
Ole W Petersen
Mina J Bissell
Judith Campisi
Sophie A Lelièvre
Buck Institute for Research on Aging · USLawrence Berkeley National Laboratory · USPurdue University West Lafayette · US

Funding

Training in Basic Research on Aging and Age-Related DiseaseT32AG000266 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI Lisa M Ellerby · 1998 to 2026
$13.8M
CELLULAR SENESCENCE AND CONTROL OF GENE EXPRESSIONR37AG009909 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CAMPISI, JUDITH · 1995 to 2015
$7.6M
Definition of the Microenvironment in Breast CancerR01CA064786 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BISSELL, MINA · 1995 to 2020
$6.1M
Definition of Microenvironment in Breast CancerR37CA064786 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BISSELL, MINA · 2009 to 2013
$2.0M
Cellular senescence and control of gene expressionR56AG009909 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI CAMPISI, JUDITH · 2017 to 2017
$592k
CELLULAR SENESCENCE AND CONTROL OF GENE EXPRESSIONR01AG009909 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI CAMPISI, JUDITH · 1990 to 1994
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NCI NIH HHS CA64786NCI NIH HHS R01 CA064786NCI NIH HHS R37 CA064786NIA NIH HHS AG00266NIA NIH HHS AG09909NIA NIH HHS R37 AG009909NIA NIH HHS R56 AG009909NIA NIH HHS T32 AG000266
6 · The paper itself

Abstract

Nuclear organization, such as the formation of specific nuclear subdomains, is generally thought to be involved in the control of cellular phenotype; however, there are relatively few specific examples of how mammalian nuclei organize during radical changes in phenotype, such as those occurring during differentiation and growth arrest. Using human mammary epithelial cells in which growth arrest is essential for morphological differentiation, we show that the arrest of cell proliferation is accompanied by a reorganization of the telomere-associated protein, TIN2, into one to three large nuclear subdomains. The large TIN2 domains do not contain telomeres and occur concomitant with the continued presence of TIN2 at telomeres. The TIN2 domains were sensitive to DNase, but not RNase, occurred frequently, but not exclusively near nucleoli, and overlapped often with dense domains containing heterochromatin protein 1gamma. Expression of truncated forms of TIN2 simultaneously prevented the formation of TIN2 domains and relaxed the stringent morphogenesis-induced growth arrest in human mammary epithelial cells. Here we show that a novel extra-telomeric organization of TIN2 is associated with the control of cell proliferation and identify TIN2 as an important regulator of mammary epithelial differentiation.

Indexed as

Blotting, WesternBreastBromodeoxyuridineCell Culture TechniquesCell DifferentiationCell NucleusCell ProliferationCells, CulturedDeoxyribonuclease IDeoxyribonucleasesEpithelial CellsHeterochromatinHumansImmunohistochemistryIn Situ Hybridization, FluorescenceKi-67 AntigenBromodeoxyuridineDeoxyribonuclease IDeoxyribonucleasesHeterochromatinKi-67 AntigenRibonuclease, PancreaticRibonucleasesTelomere-Binding ProteinsTINF2 protein, human

Identifiers

PMID15741234
PMCPMC2933191
OpenAlexW271331505

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.