Fisetin Senolytic Therapy

Fisetin Senolytic Therapy

 



Fisetin Senolytic Therapy

Risk-Benefit Analysis



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Forever Healthy Foundation gGmbH

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Version 1.2

September 18, 2019















Preface



This risk-benefit analysis is part of Forever Healthy's "Rejuvenation Now" initiative that seeks to continuously identify potential rejuvenation therapies and systematically evaluate their risks, benefits, and associated therapeutic protocols to create transparency.



Section 1: Overview 



Motivation



Senolytics are agents that selectively induce apoptosis of senescent cells. Fisetin is a flavonoid polyphenol found in many types of fruits and vegetables (Arai et al., 2000) that is believed to act as a senolytic in addition to its numerous other known benefits. Although natural senolytics are less potent, compared to the targeted senolytics, they have lower toxicity and are thus, likely to be more readily translatable to clinical medicine. This RBA focuses on the risks and benefits of using fisetin as a senolytic rather than its more common use as a supplement.



Key Questions 



This RBA seeks to answer the following questions:

  • Which health and/or longevity benefits result from the use of fisetin as a senolytic? 

  • Which risks are involved in the use of fisetin as a senolytic (general and method-specific)?

  • What are the potential risk mitigation strategies?

  • Which method or combination of methods of using fisetin as a senolytic are most effective?

  • Which of the available methods are safe for use?

  • What is the best therapeutic protocol available at the moment?  

Impatient readers may choose to skip directly to Section 6 for the conclusion and tips on practical application. 





Section 2: Methods

Analytic model



The RBA has been prepared based on the principles outlined in A Comprehensive Approach to Benefit-Risk Assessment in Drug Development ( Sarac et al., 2012 ). 



Literature search



A literature search was conducted on Pubmed and the Cochrane Library using the search terms shown in Table 1 . Titles and abstracts of the resulting studies were screened and relevant articles downloaded in full text. The references of the full-text articles were manually searched in order to identify additional trials that may have been missed by the search terms.

Because of the small number of papers available on the topic, we also searched for studies in which fisetin was found to influence any of the 6 known Senescent Cell Anti-Apoptotic Pathways (SCAPs). 



Table 1: Literature Search 

Search terms

Number of publications

fisetin AND senolytic

5

fisetin AND aging

26

fisetin AND BCL

18

fisetin AND PI3 AND AKT

3

fisetin AND apoptosis

147

fisetin AND MDM2

1

fisetin AND p53

23

fisetin AND p21

7

fisetin AND serpine

5

fisetin AND HIF

4

fisetin AND toxicity

99

fisetin AND pharmacokinetic*

41

fisetin AND benefit*

23

fisetin AND risk*

23

Other sources

Discussion with experts (names cited in the text)

A manual search of the reference lists of the selected papers 



Recommended Reading



The following sites offer information on fisetin as a senolytic at a consumer level and are useful as an introduction to the topic:



Abbreviation list



MEF

murine embryonic fibroblasts

HUVECs

human umbilical vein endothelial cells

SCAPs

senescent cell antiapoptotic pathways

SASP

senescence-associated secretory phenotype

BW

bodyweight

IMR90

human embryonic lung fibroblasts

SA-β-gal

senescence-associated beta-galactosidase

p16Ink4a

a tumor suppressor protein

p21Cip1

cell-cycle regulatory protein that Interacts with cyclin-CDK2 and -CDK4, inhibiting cell cycle progression at G1

MCP-1

monocyte chemotactic protein-1


Section 3: Existing evidence



Summary of ongoing clinical trials 



There are currently 3, phase 2 clinical trials underway (clinicaltrials.gov) and the first data is expected to be reported in about a year. The data from the phase 1 trials has not been published. All trials are being conducted by the same investigators at the Mayo clinic using the same treatment protocol. 









Summary of results from preclinical trials  (animals & in vitro)



Only 2 papers directly related to the use of fisetin as a senolytic were identified, neither of which were conducted in humans (Yousefzadeh et la., 2018; Zhu et al., 2017). The other 5 studies included in the table relate to pharmacokinetics, risk, and lifespan extension. 



Table 2: Preclinical trials



Section 4: Risk-Benefit Analysis