Evidence map›Paper›PMID 23811327›Full record

ArticleToxicology and applied pharmacology2013

Chronic cadmium exposure in vitro induces cancer cell characteristics in human lung cells.

Rachel J Person, Erik J Tokar, Yuanyuan Xu, Ruben Orihuela, Ntube N Olive Ngalame, Michael P Waalkes

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Toxicity Tolerance in the Carcinogenesis of Environmental Cadmium.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cadmium induces A549 cell migration and invasion by activating ERK.Experimental and therapeutic medicine · 2019
    Article
  20. Article
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

6 authors at 1 institution in 1 country.

Rachel J PersonInorganic Toxicology Group, National Toxicology Program Laboratory, Division of the National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
Erik J Tokar
Yuanyuan Xu
Ruben Orihuela
Ntube N Olive Ngalame
Michael P Waalkes
National Institute of Environmental Health Sciences · US

Funding

Stem Cell ToxicologyZIAES102925 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI TOKAR, ERIK · 2010 to 2021
$25.3M
Intramural NIH HHS ZIA ES102925
6 · The paper itself

Abstract

Cadmium is a known human lung carcinogen. Here, we attempt to develop an in vitro model of cadmium-induced human lung carcinogenesis by chronically exposing the peripheral lung epithelia cell line, HPL-1D, to a low level of cadmium. Cells were chronically exposed to 5 μM cadmium, a noncytotoxic level, and monitored for acquired cancer characteristics. By 20 weeks of continuous cadmium exposure, these chronic cadmium treated lung (CCT-LC) cells showed marked increases in secreted MMP-2 activity (3.5-fold), invasion (3.4-fold), and colony formation in soft agar (2-fold). CCT-LC cells were hyperproliferative, grew well in serum-free media, and overexpressed cyclin D1. The CCT-LC cells also showed decreased expression of the tumor suppressor genes p16 and SLC38A3 at the protein levels. Also consistent with an acquired cancer cell phenotype, CCT-LC cells showed increased expression of the oncoproteins K-RAS and N-RAS as well as the epithelial-to-mesenchymal transition marker protein Vimentin. Metallothionein (MT) expression is increased by cadmium, and is typically overexpressed in human lung cancers. The major MT isoforms, MT-1A and MT-2A were elevated in CCT-LC cells. Oxidant adaptive response genes HO-1 and HIF-1A were also activated in CCT-LC cells. Expression of the metal transport genes ZNT-1, ZNT-5, and ZIP-8 increased in CCT-LC cells culminating in reduced cadmium accumulation, suggesting adaptation to the metal. Overall, these data suggest that exposure of human lung epithelial cells to cadmium causes acquisition of cancer cell characteristics. Furthermore, transformation occurs despite the cell's ability to adapt to chronic cadmium exposure.

Indexed as

CadmiumCell Transformation, NeoplasticDNA DamageHumansLungLung NeoplasmsOxidative StressRespiratory MucosaTime FactorsTumor Cells, CulturedCadmium4′,6-diamidino-2-phenylindole5,5-dimethyl-1-pyrroline N-oxideAdaptationbovine serum albuminBSACadmiumCCT-LCchronic cadmium treated-lung cellsDAPIDMPOEpithelial-to-mesenchymal transitionheme oxygenase-1HIF-1AHO-1HPLHuman lung cellshuman peripheral lunghypoxia inducible factor-1 alphaimmuno-spin trappingINTISTLC50lethal concentration 50LUCAlung cancerLung cancermatrix metalloproteinase-2metallothionein-1Ametallothionein-2AMMP-2MT-1AMT-2APBSphosphate buffered salinep-iodonitro-tetrazolium violetqRT-PCRquantitative real time reverse transcription polymerase chain reactionTransformationZinc TransporterZIPZNTZrt/Irt-like Proteins

Identifiers

PMID23811327
PMCPMC3863781
OpenAlexW2006319824

What OpenQuestion holds

Textmetadata
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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.