Evidence map›Paper›PMID 26523475›Full record

ArticleCurrent protocols in toxicology2015

Use of Ciliogenesis to Detect Aneugens: The Role of Primary Cilia.

Kathyayini V Divi, Yvona Ward, Miriam C Poirier, Ofelia A Olivero

Abstract read
In one paragraph

Article in Current protocols in toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Kathyayini V DiviCarcinogen-DNA Interactions Section, LCBG, CCR, NIH, Bethesda, Maryland.
Yvona WardCell and Cancer Biology Branch, National Cancer Institute, NIH, Bethesda, Maryland.
Miriam C PoirierCarcinogen-DNA Interactions Section, LCBG, CCR, NIH, Bethesda, Maryland.
Ofelia A OliveroCarcinogen-DNA Interactions Section, LCBG, CCR, NIH, Bethesda, Maryland.

Funding

Interaction of Chemical Carcinogens and Chemotherapeutic Agents with DNAZIABC005177 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POIRIER, MIRIAM C · 2009 to 2018
$5.1M
Interaction of Chemical Carcinogens with DNAZ01BC005177 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POIRIER, MIRIAM C · 1996 to 2008
$2.1M
Intramural NIH HHS Z01 BC005177
6 · The paper itself

Abstract

Primary cilia arise from the centrosomes of quiescent or post-mitotic cells, and serve as sensory organelles that communicate mechanical and chemical stimuli from the environment to the interior of the cell. Cilium formation may, therefore, become a useful end point signaling exposure to genotoxins or aneugens. Here we have used the aneugen, zidovudine (AZT), an antiretroviral drug that induces DNA replication arrest and centrosomal amplification (>2 centrosomes per quiescent cell), to evaluate cilia formation in retinal epithelial (pigmented) cells. Since cilia are derived from centrosomes, and aneugens can induce centrosomal amplification, the production of multiple cilia arising from multiple centrosomes may reveal the aneugenic nature of the agents. Cells were exposed to AZT to induce centrosomal amplification, cultured without serum to allow the centrioles to develop cilia, and immunostained to visualize cilia and centrosomes. Nuclear DNA was stained with DAPI. Preliminary observations suggest that cells with multiple centrosomes are able to generate extra cilia.

Indexed as

AneuploidyDNA DamageAneugensCell LineCentrosomeCiliaRetinal Pigment EpitheliumZidovudineAneugensZidovudineaneugensAZTcentrosomal amplificationprimary cilia

Identifiers

PMID26523475
PMCPMC4632641

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Registered trials

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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.