Aging research from bench to bedside and beyond: What we learned from Sammy Basso

IF 7.8 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Aging Cell Pub Date : 2024-12-11 DOI:10.1111/acel.14414
Giovanna Lattanzi, Chiara Lanzuolo, Eleonora Cugudda, Lorenzo Maggi, Luisa Politano, Olaya Santiago-Fernández, Giulia Ricci, Stefano Squarzoni, Carlos Lopez-Otin, the Italian Network for Laminopathies
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引用次数: 0

Abstract

Since his teenage years, Sammy demonstrated an extraordinary awareness of his condition, far surpassing the self-awareness of many adults. With his innate positivity, he led a fulfilling life, achieving numerous goals, inspiring both patients and researchers alike. We witnessed him discuss progeria with the same rigor as any other researcher, we saw him working to understand molecular mechanisms in experimental models and clinical presentations in patients, with the final aim to find a cure. Even when discussing the prospect of a cure that hardly could have been found in a few years, he remained focused on younger patients, often stating: “I'm working for them”.

In 2017, he wrote a message intended to be read at his funeral, expressing his thoughts on living with progeria and his positive outlook on life: “I don't know when or how I will leave this world, and many may say that I have lost my battle against the disease. Don't listen to them! There was never a battle to fight; there was only a life to embrace as it is, challenging yet beautiful and extraordinary. There is no reward, no punishment, just a gift by God” and “If you'd like to remember me, don't waste too much time on various rituals, pray, of course, but also take some glasses, toast to my health and yours, and embrace joy. I've always enjoyed being around others, and that's how I'd like to be remembered”.

In the last decade, Sammy emerged as one of the most effective science communicators among young people and non-expert audiences worldwide. Together with the American Progeria Research Foundation (https://www.progeriaresearch.org/) he brought tremendous mediatic attention to this rare disease, facilitating the diagnosis of several children worldwide. His speeches raised interest in progeroid rare diseases and fostered a positive attitude towards the challenges living with progeria presents in life and life itself.

One of Sammy's dreams materialized with the establishment of the Italian Network for Laminopathies (NIL) in 2009 (https://www.igm.cnr.it/laminopatie/en/). At the age of 14 years, he was among the founders of NIL, and since then, Sammy and his association, the AIProSaB (https://www.aiprosab.org/), have encouraged all NIL partners to become increasingly engaged, providing motivation and support in various aspects, from data sharing to project drafting, from meeting organization to website development, his last impressive contribution.

As a researcher, Sammy was deeply committed to understanding the complexities of progeria. He was curious, consistently seeking new perspectives, both within and outside of mainstream science. His engagement in gene therapy for HGPS spanned from the preparation of his graduation thesis at Oviedo University in Spain until his passing. As a member of the Progeria Research Foundation, he collaborated closely with researchers trying to obtain FDA approval for the first gene therapy for progeria. A few years ago, he was engaged in obtaining EMA approval of lonafarnib, now available as at-home oral therapy for Progeria patients. He was recently engaged in the working group for the optimization of surgical interventions to relieve critical aortic stenosis in HGPS patients (Gordon et al., 2024). Sammy directly contributed with both his brilliant mind and his own hands to the development of a CRISPR/Cas9-based therapy for HGPS which was successfully tested in a murine model of progeria (Osorio et al., 2011; Santiago-Fernández et al., 2019). His research at the CNR Institute of Molecular Genetics in Bologna also included studying interleukin 6-dependent mechanisms in HGPS (Squarzoni et al., 2021) and exploring potential immunological therapies, a focus that began with his Master's thesis in Molecular Biology, which he completed with honors at the University of Padua; as well as work on fat loss in HGPS, a study which is currently in submission.

In all these endeavors, his optimism, cheerfulness, humor, and kindness illuminated the lives of all who had the privilege of knowing him.

He leaves behind a rich legacy of research, compassion, and inspiration. Perhaps, the most significant lesson we learned from Sammy, is to have a fresh and open perspective on science, characterized by a shared curiosity and enthusiasm, a positive view of new findings, realism, and a determination to overcome obstacles with rigorous and open-minded approaches.

We honor Sammy's memory with deep gratitude for the inspiration he provided and the impact he made in the world of science and beyond.

All authors contributed equally to this article.

No conflicts of interest.

Abstract Image

衰老研究从实验到临床再到更远的地方:我们从萨米·巴索那里学到了什么。
从十几岁起,萨米就对自己的状况表现出了超乎寻常的意识,远远超过了许多成年人的自我意识。由于他天生的积极,他过着充实的生活,实现了许多目标,激励了患者和研究人员。我们看到他像其他研究人员一样严谨地讨论早衰症,我们看到他努力了解实验模型中的分子机制和患者的临床表现,最终目标是找到治疗方法。即使在讨论几年之内几乎不可能找到治愈方法的前景时,他仍然把重点放在年轻患者身上,经常说:“我在为他们工作”。2017年,他写了一篇遗言,打算在葬礼上宣读,表达了他对早衰症的生活看法和积极的人生观:“我不知道何时或如何离开这个世界,许多人可能会说我已经输掉了与这种疾病的斗争。别听他们的!从来没有战斗要打;生活就是这样,充满挑战却又美丽非凡。没有奖励,没有惩罚,只是上帝的礼物”和“如果你想记住我,不要浪费太多时间在各种仪式上,当然,祈祷,但也要拿一些杯子,为我和你的健康干杯,拥抱快乐。”我总是喜欢和别人在一起,这也是我希望别人记住我的方式。”在过去的十年里,萨米成为了全世界年轻人和非专业观众中最有效的科学传播者之一。与美国早衰症研究基金会(https://www.progeriaresearch.org/)一起,他引起了媒体对这种罕见疾病的极大关注,促进了全世界几个儿童的诊断。他的演讲提高了人们对罕见的早衰症的兴趣,并培养了一种积极的态度来面对生活中早衰症带来的挑战。2009年,意大利椎板病网络(NIL)的成立实现了萨米的一个梦想(https://www.igm.cnr.it/laminopatie/en/)。14岁时,他是NIL的创始人之一,从那时起,Sammy和他的协会AIProSaB (https://www.aiprosab.org/)鼓励所有NIL合作伙伴越来越多地参与其中,在各个方面提供动力和支持,从数据共享到项目起草,从会议组织到网站开发,这是他最后一次令人印象深刻的贡献。作为一名研究人员,萨米一直致力于了解早衰症的复杂性。他很好奇,不断寻求新的视角,无论是在主流科学领域内还是在主流科学之外。从在西班牙奥维耶多大学准备毕业论文到去世,他一直致力于HGPS的基因治疗。作为早衰症研究基金会的成员,他与研究人员密切合作,试图获得FDA批准的第一个早衰症基因疗法。几年前,他致力于获得lonafarnib的EMA批准,现在可以作为早衰症患者的家庭口服疗法。他最近参与了优化外科干预措施以缓解HGPS患者严重主动脉狭窄的工作组(Gordon et al., 2024)。Sammy以其聪明的头脑和自己的双手直接参与了基于CRISPR/ cas9的HGPS治疗方法的开发,并成功地在早衰症小鼠模型中进行了测试(Osorio et al., 2011;Santiago-Fernández等人,2019)。他在博洛尼亚CNR分子遗传学研究所的研究还包括研究HGPS中白细胞介素6依赖机制(Squarzoni等人,2021年)和探索潜在的免疫疗法,这一重点始于他在帕多瓦大学(University of Padua)完成的分子生物学硕士论文;以及对HGPS中脂肪减少的研究,该研究目前正在提交。在所有这些努力中,他的乐观、开朗、幽默和善良照亮了所有有幸认识他的人的生活。他留下了丰富的研究遗产、同情心和灵感。也许,我们从萨米身上学到的最重要的一课,是对科学有一个新鲜和开放的视角,其特点是共同的好奇心和热情,对新发现的积极看法,现实主义,以及用严谨和开放的方法克服障碍的决心。我们对萨米的记忆表示敬意,并对他所提供的灵感和他在科学界及其他领域所产生的影响深表感激。所有作者对这篇文章贡献均等。没有利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
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