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Publication : PKK deletion in basal keratinocytes promotes tumorigenesis after chemical carcinogenesis.

First Author  Chen L Year  2018
Journal  Carcinogenesis Volume  39
Issue  3 Pages  418-428
PubMed ID  29186361 Mgi Jnum  J:258836
Mgi Id  MGI:6147901 Doi  10.1093/carcin/bgx120
Citation  Chen L, et al. (2018) PKK deletion in basal keratinocytes promotes tumorigenesis after chemical carcinogenesis. Carcinogenesis 39(3):418-428
abstractText  Squamous cell carcinoma (SCC) of the skin is a keratinocyte malignancy characterized by tumors presenting on sun-exposed areas with surgery being the mainstay treatment. Despite advances in targeted therapy in other skin cancers, such as basal cell carcinoma and melanoma, there have been no such advances in the treatment of SCC. This is partly due to an incomplete knowledge of the pathogenesis of SCC. We have recently identified a protein kinase C-associated kinase (PKK) as a potential tumor suppressor in SCC. We now describe a novel conditional PKK knockout mouse model, which demonstrates that PKK deficiency promotes SCC formation during chemically induced tumorigenesis. Our results further support that PKK functions as a tumor suppressor in skin keratinocytes and is important in the pathogenesis of SCC of the skin. We further define the interactions of keratinocyte PKK with TP63 and NF-kappaB signaling, highlighting the importance of this protein as a tumor suppressor in SCC development.
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