SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-95977"
 

Search: onr:"swepub:oai:DiVA.org:uu-95977" > Valproic acid terat...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Valproic acid teratogenicity: a toxicogenomics approach

Kultima, Kim (author)
Uppsala universitet,Avdelningen för toxikologi
Nyström, Anna-Maja (author)
Uppsala universitet,Avdelningen för toxikologi
Scholz, Birger (author)
Uppsala universitet,Avdelningen för toxikologi
show more...
Gustafson, Anne-Lee (author)
Uppsala universitet,Avdelningen för toxikologi
Dencker, Lennart (author)
Uppsala universitet,Avdelningen för toxikologi
Stigson, Michael (author)
Uppsala universitet,Avdelningen för toxikologi
show less...
 (creator_code:org_t)
2004
2004
English.
In: Journal of Environmental Health Perspectives. - 0091-6765 .- 1552-9924. ; 112:12, s. 1225-1235
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Embryonic development is a highly coordinated set of processes that depend on hierarchies of signaling and gene regulatory networks, and the disruption of such networks may underlie many cases of chemically induced birth defects. The antiepileptic drug valproic acid (VPA) is a potent inducer of neural tube defects (NTDs) in human and mouse embryos. As with many other developmental toxicants however, the mechanism of VPA teratogenicity is unknown. Using microarray analysis, we compared the global gene expression responses to VPA in mouse embryos during the critical stages of teratogen action in vivo with those in cultured P19 embryocarcinoma cells in vitro. Among the identified VPA-responsive genes, some have been associated previously with NTDs or VPA effects [vinculin, metallothioneins 1 and 2 (Mt1, Mt2), keratin 1-18 (Krt1-18)], whereas others provide novel putative VPA targets, some of which are associated with processes relevant to neural tube formation and closure [transgelin 2 (Tagln2), thyroid hormone receptor interacting protein 6, galectin-1 (Lgals1), inhibitor of DNA binding 1 (Idb1), fatty acid synthase (Fasn), annexins A5 and A11 (Anxa5, Anxa11)], or with VPA effects or known molecular actions of VPA (Lgals1, Mt1, Mt2, Id1, Fasn, Anxa5, Anxa11, Krt1-18). A subset of genes with a transcriptional response to VPA that is similar in embryos and the cell model can be evaluated as potential biomarkers for VPA-induced teratogenicity that could be exploited directly in P19 cell-based in vitro assays. As several of the identified genes may be activated or repressed through a pathway of histone deacetylase (HDAC) inhibition and specificity protein 1 activation, our data support a role of HDAC as an important molecular target of VPA action in vivo.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

biomarker
embryocarcinoma
galectin-1
histone deacetylase
in vitro toxicology
metallothionein
microarray
mouse embryo
neural tube defect
Sp1
teratogen
valproic acid
vinculin
PHARMACY
FARMACI

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view