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RESEARCH PAPER / 2025-01-03

SNP rs6543176 is associated with extreme human longevity but increased risk for cancer.

Anastasia Gurinovich, Zeyuan Song, Harold Bae, Anastasia Leshchyk, Mengze Li, Hannah Lords, Stacy L Andersen, Marianne Nygaard, Kaare Christensen, E Warwick Daw, Konstantin G Arbeev, Michael R Brent, Thomas T Perls, Paola Sebastiani

Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, 02111, USA. [email protected]. · pubmed

Abstract

Using whole-genome sequencing (WGS) might offer insights into rare genetic variants associated with healthy aging and extreme longevity (EL), potentially pointing to useful therapeutic targets. In this study, we conducted a genome-wide association study using WGS data from the Long Life Family Study and identified a novel longevity-associated variant rs6543176 in the SLC9A2 gene. This SNP also showed a significant association with reduced hypertension risk and an increased, though not statistically significant, cancer risk. The association with cancer risk was replicated in the UK Biobank and FinnGen. Metabolomic analyses linked the rs6543176 longevity allele to higher serine levels, potentially associated with delayed mortality. Our findings warrant further investigation of SLC9A2's role in both longevity and cancer susceptibility, and they highlight the need for careful evaluation in developing anti-aging therapies based on EL-associated alleles.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper identifies a genetic variant associated with extreme longevity and explores its implications for both longevity and cancer risk. While it contributes to the understanding of genetic factors in aging, the findings are primarily associative and do not directly address the mechanisms of aging or propose therapeutic interventions. Thus, it represents solid research but with limited impact on the field of longevity research.

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