Deregulated Adhesion Program in Palatal Keratinocytes of Orofacial Cleft Patients.
Ontology highlight
ABSTRACT: Orofacial clefts (OFCs) are the most frequent craniofacial birth defects. An orofacial cleft (OFC) occurs as a result of deviations in palatogenesis. Cell proliferation, differentiation, adhesion, migration and apoptosis are crucial in palatogenesis. We hypothesized that deregulation of these processes in oral keratinocytes contributes to OFC. We performed microarray expression analysis on palatal keratinocytes from OFC and non-OFC individuals. Principal component analysis showed a clear difference in gene expression with 24% and 17% for the first and second component, respectively. In OFC cells, 228 genes were differentially expressed (p < 0.001). Gene ontology analysis showed enrichment of genes involved in β1 integrin-mediated adhesion and migration, as well as in P-cadherin expression.
SUBMITTER: Mammadova A
PROVIDER: S-EPMC6895790 | biostudies-literature | 2019 Oct
REPOSITORIES: biostudies-literature
ACCESS DATA