Venniyoor Ajit
Department of Medical Oncology, National Oncology Centre, The Royal Hospital, Muscat, Oman.
Front Nutr. 2020 Jun 5;7:81. doi: 10.3389/fnut.2020.00081. eCollection 2020.
The modern obesity epidemic with associated disorders of metabolism and cancer has been attributed to the presence of "thrifty genes". In the distant past, these genes helped the organism to improve energy efficiency and store excess energy safely as fat to survive periods of famine, but in the present day obesogenic environment, have turned detrimental. I propose PTEN as the likely gene as it has functions that span metabolism, cancer and reproduction, all of which are deranged in obesity and insulin resistance. The activity of PTEN can be calibrated by availability of nutrients by the methylation arm of the epigenetic pathway. Deficiency of protein and choline has been shown to upregulate DNA methyltransferases (DNMT), especially 1 and 3a; these can then methylate promoter region of PTEN and suppress its expression. Thus, the gene is tuned like a metabolic rheostat proportional to the availability of specific nutrients, and the resultant "dose" of the protein, which sits astride and negatively regulates the insulin-PI3K/AKT/mTOR pathway, decides energy usage and proliferation. This "fixes" the metabolic capacity of the organism periconceptionally to a specific postnatal level of nutrition, but when faced with a discordant environment, leads to obesity related diseases.
现代肥胖流行以及相关的代谢紊乱和癌症被归因于“节俭基因”的存在。在遥远的过去,这些基因帮助生物体提高能量效率,并将多余的能量安全地储存为脂肪,以度过饥荒时期,但在当今的致肥胖环境中,却变得有害。我认为PTEN可能是这个基因,因为它的功能涵盖代谢、癌症和生殖,而这些在肥胖和胰岛素抵抗中均出现紊乱。PTEN的活性可通过表观遗传途径的甲基化分支,根据营养物质的可利用性进行校准。蛋白质和胆碱缺乏已被证明会上调DNA甲基转移酶(DNMT),尤其是DNMT1和3a;然后这些酶会使PTEN的启动子区域甲基化并抑制其表达。因此,该基因就像一个代谢变阻器,根据特定营养物质的可利用性进行调节,而由此产生的蛋白质“剂量”,它横跨并负向调节胰岛素 - PI3K/AKT/mTOR通路,决定能量利用和细胞增殖。这在受孕期间将生物体的代谢能力“设定”到特定的产后营养水平,但当面对不匹配的环境时,就会导致肥胖相关疾病。