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• W2102535562 abstract "Fracture healing requires the cooperation of multiple molecular signaling pathways. To better understand this cascade of transcriptional events, we compared the gene expression profiles between intact bone and fractured bone at days 1, 2, and 4 using a rat femur model of bone healing. Cluster analysis identified several groups of genes with dynamic temporal expression patterns and stage-specific functions. The immediate-response genes are highlighted by binding activity, transporter activity, and energy derivation. We consider these activities as critical signals for initiation of fracture healing. The continuously increased genes are characterized by those directly involved in bone repair, thus, representing bone specific forefront workers. The constantly upregulated genes tend to regulate general cell growth and are enriched with genes that are involved in tumorigenesis, suggesting common pathways between two processes. The constantly downregulated genes predominantly involve immune response, the significance of which remains for further investigation. Knowledge acquired through this analysis of transcriptional activities at the early stage of bone healing will contribute to our understanding of fracture repair and bone-related pathological conditions." @default.
• W2102535562 created "2016-06-24" @default.
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• W2102535562 date "2005-01-01" @default.
• W2102535562 modified "2023-10-17" @default.
• W2102535562 title "Early signals for fracture healing" @default.
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• W2102535562 doi "https://doi.org/10.1002/jcb.20373" @default.
• W2102535562 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15759269" @default.
• W2102535562 hasPublicationYear "2005" @default.
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