Evidence map›Paper›PMID 18037969›Full record

ArticleMolecular medicine (Cambridge, Mass.)

Neoplastic transformation of human small airway epithelial cells induced by arsenic.

Gengyun Wen, Gloria M Calaf, Michael A Partridge, Carlos Echiburú-Chau, Yongliang Zhao, Sarah Huang, Yunfei Chai, Bingyan Li, Burong Hu, Tom K Hei

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-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

18 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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  6. Arsenic is cytotoxic and genotoxic to primary human lung cells.Mutation research. Genetic toxicology and environmental mutagenesis · 2014
    Article
  7. Review
  8. Article
  9. Article
  10. Arsenic, asbestos and radon: emerging players in lung tumorigenesis.Environmental health : a global access science source · 2012
    Review
  11. Article
  12. Article
  13. Article
  14. Article
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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

10 authors at 3 institutions in 3 countries.

Gengyun WenCenter for Radiological Research, Columbia University Medical Center, New York, NY 10032, USA. gw2154@columbia.edu
Gloria M Calaf
Michael A Partridge
Carlos Echiburú-Chau
Yongliang Zhao
Sarah Huang
Yunfei Chai
Bingyan Li
Burong Hu
Tom K Hei
Columbia University Irving Medical Center · USUniversity of Tarapacá · CLSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human small airway epithelial cells (SAECs) previously immortalized with human telomerase reverse transcriptase (h-TERT) were continuously treated with sodium arsenite at a dose of 0.5 microg/mL in culture for up to 6 months. Arsenic-treated cells progressively displayed an increase in transformed phenotype including enhanced growth saturation density, plating efficiency, and anchorage-independent growth and invasion capability compared with their nontreated control cells. To determine whether arsenic-induced cell transformation was associated with genomic instability, treated and control cells were also analyzed for micronuclei formation. A 4.8-fold increase in micronuclei incidence in arsenic-treated cells was detected in conjunction with increased N-phosphonacetyl-l-aspartate (PALA)-resistant characteristics. In addition, arsenic-treated cells showed an increase in c-H-ras, c-myc, and c-fos protein expression relative to controls. The change in oncoprotein expression correlated with a decrease in wild-type p53 expression and hyperphosphorylated retinoblastoma. Taken together, these results strongly suggest that h-TERT immortalized human small airway epithelial cells underwent step-wise transformation after inorganic arsenic treatment.

Indexed as

ArsenitesCell DifferentiationCell Line, TransformedCell ProliferationCell Transformation, NeoplasticEpithelial CellsHumansMicronuclei, Chromosome-DefectiveProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-mycProto-Oncogene Proteins p21(ras)Respiratory MucosaSodium CompoundsTelomeraseTumor Suppressor Protein p53ArsenitesProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-mycProto-Oncogene Proteins p21(ras)sodium arseniteSodium CompoundsTelomeraseTERT protein, humanTumor Suppressor Protein p53

Identifiers

PMID18037969
PMCPMC2082132
OpenAlexW46853567

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.