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Series GSE4066 Query DataSets for GSE4066
Status Public on Jul 01, 2006
Title Erbb2 regulates inflammation and proliferation in the skin after ultraviolet irradiation.
Organism Mus musculus
Experiment type Expression profiling by array
Summary Exposure to ultraviolet (UV) irradiation is the major cause of nonmelanoma skin cancer, the most common form of cancer in the United States. UV irradiation has a variety of effects on the skin associated with carcinogenesis, including DNA damage and effects on signal transduction. The alterations in signaling caused by UV regulate inflammation, cell proliferation, and apoptosis. UV also activates the orphan receptor tyrosine kinase and proto-oncogene Erbb2 (HER2/neu). In this study, we demonstrate that the UV-induced activation of Erbb2 regulates the response of the skin to UV. Inhibition or knockdown of Erbb2 before UV irradiation suppressed cell proliferation, cell survival, and inflammation after UV. In addition, Erbb2 was necessary for the UV-induced expression of numerous proinflammatory genes that are regulated by the transcription factors nuclear factor-kappaB and Comp1, including interleukin-1beta, prostaglandin-endoperoxidase synthase 2 (Cyclooxygenase-2), and multiple chemokines. These results reveal the influence of Erbb2 on the UV response and suggest a role for Erbb2 in UV-induced pathologies such as skin cancer.
Keywords: time course, ultraviolet irradiation, UV, erbB2, mouse skin
 
Overall design The dorsal skin of adult female CD-1 mice was clipped one day before treatment and shaved on the day of treatment. DMSO or 4 mg AG825 dissolved in DMSO was applied topically to the shaved back of the mice 2 h prior to exposure to 10 kJ/m^2 UV or sham irradiation. The UV dose was approximately 30% UVA, 70% UVB and <1% UVC, with a total output of 470 μW/cm^2. Flash frozen skin was removed and total RNA expracted with TRIzol reagent (Invitrogen) and further purified with an RNeasy kit (Qiagen). Amplification, reverse-transcription, biotinylation, and hybridization were all carried out under standard conditions and procedures recommended by the manufacturer.
 
Contributor(s) Madson JG, Hansen LA
Citation(s) 17003495
Submission date Jan 19, 2006
Last update date Jan 08, 2019
Contact name Laura A Hansen
E-mail(s) lhansen@creighton.edu
Phone 402-280-4085
Fax 402-280-2690
Organization name Creighton University School of Medicine
Department Biomedical Sciences
Street address 2500 California Plaza
City Omaha
State/province NE
ZIP/Postal code 68178
Country USA
 
Platforms (1)
GPL339 [MOE430A] Affymetrix Mouse Expression 430A Array
Samples (23)
GSM93177 DMSO-treated, Sham UV, Replicate A
GSM93178 DMSO-treated, Sham UV, Replicate B
GSM93179 DMSO-treated, Sham UV, Replicate C
Relations
BioProject PRJNA95191

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE4066_GCOS_derived_signal.txt 3.8 Mb (ftp)(http) TXT
GSE4066_RAW.tar 80.5 Mb (http)(custom) TAR (of CEL)
GSE4066_dChip_derived_signal.txt 5.2 Mb (ftp)(http) TXT

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