by Chen Na, Chinese Academy of Sciences
The intracellular mechanisms that support Rutin to function as a novel senomorphic agent in antiaging interventions. Credit: Dr. SUN’s group
Since the discovery of hallmark features of senescence such as cell cycle arrest, apoptosis resistance and development of a senescence-associated secretory phenotype (SASP), efforts in understanding how senescent cells drive physiological and pathological aging have grown exponentially. The accumulation of senescent cells in aging individuals is associated with increased occurrence of age-associated pathologies that contribute to poor health, frailty, and mortality.
Targeting senescent cells with senolytics or senomorphics hold the potential to mitigate the vast majority of age-related disorders. Examples of senopathies include but are not limited to neurodegenerative, cardiovascular, metabolic, musculoskeletal, liver, lung and kidney diseases.
However, the major challenge in developing novel senotherapies is the paucity of antiaging agents that have decent safety profiles, a condition that limits development of many pharmacological pipelines.
Prof. Sun Yu and his colleagues at Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences recently performed large scale screening of a natural medicinal agent library for senotherapeutic candidates and validated several agents, which showed their excellent potential to serve as senomorphics. The study, titled “Rutin is a potent senomorphic agent to target senescent cells and can improve chemotherapeutic efficacy,” was published online in Aging Cell on July 20, 2023.
Rutin, a small molecule phytochemical component enriched in an array of plants, exhibited an outstanding capacity in targeting senescent cells by reducing the expression of a full spectrum SASP.
In-depth investigation revealed that Rutin mainly curtails the acute stress-associated phenotype (ASAP) by specifically abrogating the interaction between ATM and HIF1α, as well as the interaction between ATM and TRAF6, critical events that together underlie the ASAP development until the phenotype culminates in the form of a typical SASP.
Such a mechanism allows Rutin to effectively control the impact of senescent cells in generating a highly pro-inflammatory extracellular microenvironment, which frequently promotes the incidence and exacerbation of many age-related diseases in the advanced life stage of humans.
Preclinical data of Sun’s lab suggested that Rutin has an excellent efficacy in promoting chemotherapeutic outcomes, such as in the case of mitoxantrone treatment. Although cancer cells also become senescent in response to various chemotherapeutic regimens, they cannot repopulate and expand continuously within tumor foci during and/or after anticancer regimens. However, stromal cell subpopulations tend to become senescent in response to anticancer treatments, and confer surviving cancer cells with rema
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