Baramiya Mamuka G, Baranov Eugene, Saburina Irina, Salnikov Lev
AntiCancer, Inc., San Diego, CA 92111, USA.
Institute of General Pathology & Pathophysiology, Moscow, Russia.
Future Sci OA. 2020 Jun 30;6(8):FSO610. doi: 10.2144/fsoa-2020-0085.
In the first part of our study, we substantiated that the embryonic reontogenesis and malignant growth (disintegrating growth) pathways are the same, but occur at different stages of ontogenesis, this mechanism is carried out in opposite directions. Cancer has been shown to be epigenetic-blocked redifferentiation and unfinished somatic embryogenesis. We formulated that only this approach of aging elimination has real prospects for a future that is fraught with cancer, as we will be able to convert this risk into a rejuvenation process through the continuous cycling of cell dedifferentiation-differentiation processes (permanent remorphogenesis). Here, we continue to develop the idea of looped ontogenesis and formulate the concept of the rejuvenation circle.
在我们研究的第一部分,我们证实胚胎再生发育和恶性生长(分解性生长)途径是相同的,但发生在个体发育的不同阶段,且这一机制是反向进行的。癌症已被证明是表观遗传阻断的再分化和未完成的体细胞胚胎发生。我们提出,只有这种消除衰老的方法对于充满癌症风险的未来才具有真正的前景,因为我们将能够通过细胞去分化 - 分化过程的持续循环(永久重塑)将这种风险转化为年轻化过程。在此,我们继续拓展循环个体发育的理念,并阐述年轻化循环的概念。