Biological mechanisms of bone and cartilage remodelling—genomic perspective

International Orthopaedics - Tập 31 - Trang 799-805 - 2007
F. Borovecki1, N. Pecina-Slaus2, S. Vukicevic3
1Center for Functional Genomics, School of Medicine, University Hospital Center, University of Zagreb, Zagreb, Croatia
2Department of Biology, School of Medicine, University of Zagreb, Zagreb, Croatia
3Department of Anatomy, School of Medicine, University of Zagreb, Zagreb, Croatia

Tóm tắt

Rapid advancements in the field of genomics, enabled by the achievements of the Human Genome Project and the complete decoding of the human genome, have opened an unimaginable set of opportunities for scientists to further unveil delicate mechanisms underlying the functional homeostasis of biological systems. The trend of applying whole-genome analysis techniques has also contributed to a better understanding of physiological and pathological processes involved in homeostasis of bone and cartilage tissues. Gene expression profiling studies have yielded novel insights into the complex interplay of osteoblast and osteoclast regulation, as well as paracrine and endocrine control of bone and cartilage remodelling. Mechanisms of new bone formation responsible for fracture healing and distraction osteogenesis, as well as healing of joint cartilage defects, have also been extensively studied. Microarray experiments have been especially useful in studying pathological processes involved in diseases such as osteoporosis or bone tumours. Existing results show that microarrays hold great promise in areas such as identification of targets for novel therapies or development of new biomarkers and classifiers in skeletal diseases.

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