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Biological mechanisms of bone and cartilage remodelling—genomic perspective

机译:骨骼和软骨重塑的生物学机制—基因组学观点

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摘要

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.
机译:人类基因组计划的成就和人类基因组的完整解码,推动了基因组学领域的飞速发展,这为科学家进一步揭示生物系统功能稳态的基础机制提供了难以想象的机遇。应用全基因组分析技术的趋势也有助于更好地了解与骨骼和软骨组织动态平衡有关的生理和病理过程。基因表达谱研究对成骨细胞和破骨细胞调节的复杂相互作用以及骨骼和软骨重塑的旁分泌和内分泌控制产生了新的见解。还已经广泛研究了负责骨折愈合和牵张成骨以及关节软骨缺损愈合的新骨形成机制。微阵列实验在研究与诸如骨质疏松症或骨肿瘤之类的疾病有关的病理过程中特别有用。现有结果表明,微阵列在诸如确定新疗法的靶标或开发骨骼疾病中新的生物标记物和分类器等领域具有广阔的前景。

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