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Deregulation of CRTCs in Aging and Age-related Disease Risk

机译:在年龄和与年龄有关的疾病风险中放松CRTC的管制

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摘要

Advances in public health in the last century have seen a sharp increase in human life expectancy. With these changes have come increased incidence of age-related pathologies and health burdens in the elderly. Patient age is the biggest risk factor for multiple chronic conditions that often occur simultaneously within one individual. An alternative to disease centric therapeutic approaches is that of ‘geroscience’, which aims to define molecular mechanisms that link age to overall disease risk. One such mechanism is deregulation of CREB-regulated transcriptional coactivators, CRTCs. Initially identified for their role in modulating CREB transcription, the last five years has seen an expansion in knowledge of new cellular regulators and roles of CRTCs beyond CREB. CRTCs have been shown to modulate organismal aging in C. elegans and to impact age-related diseases in humans. Here, we discuss CRTC deregulation as a new driver of aging, and integrating link between age and disease risk.
机译:上个世纪,公共卫生的进步使人们的预期寿命急剧增加。随着这些变化,老年人与年龄有关的病理和健康负担的发生率增加。患者年龄是经常在一个人中同时发生的多种慢性病的最大危险因素。以疾病为中心的治疗方法的另一种选择是“基因科学”,它旨在定义将年龄与总体疾病风险联系起来的分子机制。一种这样的机制是CREB调节的转录共激活剂CRTC的失调。最初由于其在调节CREB转录中的作用而被确定,最近五年来,除了CREB以外,新细胞调节剂的知识和CRTC的作用也在不断扩展。 CRTC已显示可调节秀丽隐杆线虫的机体衰老并影响人类与年龄有关的疾病。在这里,我们将CRTC放松管制视为衰老的新驱动力,并将年龄与疾病风险之间的联系整合在一起。

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