Evidence map›Paper›PMID 15793298›Full record

ArticleThe American journal of pathology2005

Chromatin organization measured by AluI restriction enzyme changes with malignancy and is regulated by the extracellular matrix and the cytoskeleton.

Andrew J Maniotis, Klara Valyi-Nagy, John Karavitis, Jonas Moses, Viveka Boddipali, Ying Wang, Rafael Nuñez, Suman Setty, Zarema Arbieva, Mina J Bissell and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Gene expression in the third dimension: the ECM-nucleus connection.Journal of mammary gland biology and neoplasia · 2010
    Review
  10. Article
  11. Review
  12. Authenticating cell lines in ophthalmic research laboratories.Investigative ophthalmology & visual science · 2008
    Review
  13. Micromechanical studies of mitotic chromosomes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2008
    Review
  14. Modeling the behavior of uveal melanoma in the liver.Investigative ophthalmology & visual science · 2007
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Andrew J ManiotisDepartment of Pathology, University of Illinois at Chicago, 1819 W. Polk Street, 446 CMW (MC 847), Chicago, IL 60612, USA. amanioti@uic.edu
Klara Valyi-Nagy
John Karavitis
Jonas Moses
Viveka Boddipali
Ying Wang
Rafael Nuñez
Suman Setty
Zarema Arbieva
Mina J Bissell
Robert Folberg
University of Illinois Chicago · USLawrence Berkeley National Laboratory · US

Funding

MICROCIRCULATION OF UVEAL MELANOMAR01EY010457 · NEI · UNIVERSITY OF IOWA · PI FOLBERG, ROBERT · 1994 to 2007
$2.6M
NEI NIH HHS EY10457NEI NIH HHS R01 EY010457
6 · The paper itself

Abstract

Given that expression of many genes changes when cells become malignant or are placed in different microenvironments, we asked whether these changes were accompanied by global reorganization of chromatin. We reasoned that sequestration or exposure of chromatin-sensitive sites to restriction enzymes could be used to detect this reorganization. We found that AluI-sensitive sites of nonmalignant cells were relatively more exposed compared to their malignant counterparts in cultured cells and human tumor samples. Changes in exposure and sequestration of AluI-sensitive sites in normal fibroblasts versus fibrosarcoma or those transfected with oncogenes, nonmalignant breast cells versus carcinomas and poorly metastatic versus highly invasive melanoma were shown to be independent of the cell cycle and may be influenced by proteins rich in disulfide bonds. Remarkably, regardless of degree of malignancy, AluI-sensitive sites became profoundly sequestered when cells were incubated with laminin, Matrigel, or a circular RGD peptide (RGD-C), but became exposed when cells were placed on collagen I or in serum-containing medium. Disruption of the actin cytoskeleton led to exposure, whereas disruption of microtubules or intermediate filaments exerted a sequestering effect. Thus, AluI-sensitive sites are more sequestered with increasing malignant behavior, but the sequestration and exposure of these sites is exquisitely sensitive to information conferred to the cell by molecules and biomechanical forces that regulate cellular and tissue architecture.

Indexed as

DNA Restriction EnzymesCell Culture TechniquesCell Line, TumorCell Transformation, NeoplasticChromatinCollagenCytoskeletonDNA, NeoplasmDrug CombinationsExtracellular MatrixFlow CytometryGene Expression Regulation, NeoplasticHumansLamininMicroscopy, Electron, TransmissionNeoplasmsChromatinCollagenDNA, NeoplasmDNA Restriction EnzymesDrug CombinationsLamininmatrigelProteoglycans

Identifiers

PMID15793298
PMCPMC1602386
OpenAlexW1981912870

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.