TY - JOUR
T1 - Einstein-Nathan Shock Center
T2 - translating the hallmarks of aging to extend human health span
AU - Cuervo, Ana Maria
AU - Huffman, Derek M.
AU - Vijg, Jan
AU - Milman, Sofiya
AU - Singh, Rajat
AU - Barzilai, Nir
N1 - Funding Information:
The Nathan Shock Center of Excellence for the basic Biology of Aging (NIH NIA P30AG038072), the Einstein-Paul Glenn Foundation for Medical Research Center for the Biology of Human Aging
Funding Information:
The Einstein-Nathan Shock Center of Excellence for the basic Biology of Aging is supported by the NIH NIA grant P30AG038072.
Publisher Copyright:
© 2021, American Aging Association.
PY - 2021/10
Y1 - 2021/10
N2 - The overarching mission of the Einstein-Nathan Shock Center (E-NSC) is to make scientific discoveries in geroscience, leveraging on the expertise in our center in 6 out of the 7 pillars of aging, and to translate their effects towards drug discovery. The relevance of this basic biology of aging discoveries to humans will be confirmed through the unique gero-human resource at E-NSC. This is achieved through services provided by E-NSC, connectivity among its members, attracting worldwide investigators, and providing them with the opportunities to become future leaders. The two central components of the E-NSC are (a) cutting-edge research programs and (b) unique E-NSC research support cores. E-NSC scientists lead NIH-supported cutting-edge research programs that integrate key hallmarks of aging including proteostasis/autophagy, metabolism/inflammaging, genetic/epigenetics, stem cells/regeneration, and translational aging/longevity. Since the inception of the E-NSC, the well-integrated, collaborative, and innovative nature of the multiple supporting state-of-the-art E-NSC research cores form the bedrock of research success at the E-NSC. The three state-of-the-art E-NSC research cores, (i) Proteostasis of Aging Core (PAC), (ii) the Health Span Core (HSC), and (iii) the Human Multi-Omics Core (HMOC), have allowed impressive expansion of translational biological research programs. Expansion was facilitated through the wealth of data coming from genomics/proteomics and metabolomic analysis on human longevity studies, due to access to a variety of biological samples from elderly subjects in clinical trials with aging-targeting drugs, and new drug design services via the PAC to target the hallmarks of aging.
AB - The overarching mission of the Einstein-Nathan Shock Center (E-NSC) is to make scientific discoveries in geroscience, leveraging on the expertise in our center in 6 out of the 7 pillars of aging, and to translate their effects towards drug discovery. The relevance of this basic biology of aging discoveries to humans will be confirmed through the unique gero-human resource at E-NSC. This is achieved through services provided by E-NSC, connectivity among its members, attracting worldwide investigators, and providing them with the opportunities to become future leaders. The two central components of the E-NSC are (a) cutting-edge research programs and (b) unique E-NSC research support cores. E-NSC scientists lead NIH-supported cutting-edge research programs that integrate key hallmarks of aging including proteostasis/autophagy, metabolism/inflammaging, genetic/epigenetics, stem cells/regeneration, and translational aging/longevity. Since the inception of the E-NSC, the well-integrated, collaborative, and innovative nature of the multiple supporting state-of-the-art E-NSC research cores form the bedrock of research success at the E-NSC. The three state-of-the-art E-NSC research cores, (i) Proteostasis of Aging Core (PAC), (ii) the Health Span Core (HSC), and (iii) the Human Multi-Omics Core (HMOC), have allowed impressive expansion of translational biological research programs. Expansion was facilitated through the wealth of data coming from genomics/proteomics and metabolomic analysis on human longevity studies, due to access to a variety of biological samples from elderly subjects in clinical trials with aging-targeting drugs, and new drug design services via the PAC to target the hallmarks of aging.
KW - Autophagy
KW - Genomics
KW - Health span
KW - Metabolism
KW - Parabiosis
KW - Proteomics
KW - Proteostasis
UR - http://www.scopus.com/inward/record.url?scp=85113989071&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85113989071&partnerID=8YFLogxK
U2 - 10.1007/s11357-021-00428-9
DO - 10.1007/s11357-021-00428-9
M3 - Article
C2 - 34463901
AN - SCOPUS:85113989071
SN - 2509-2715
VL - 43
SP - 2167
EP - 2182
JO - GeroScience
JF - GeroScience
IS - 5
ER -