《科学》 第393卷 第6817期 · 2026年9月17日 · 中文解读
追溯过去遗传学:罕见基因变异与肺癌风险的历史
In search of past genetics · Stephen Chanock
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这篇讲什么
一项基于23andMe数据库的人口规模分析,研究了与肺癌高风险相关的罕见种系变异T790M的分布、效应和历史。
原文开头
Population data uncover the history of a rare genetic variant associated with high risk of lung cancer Smoking-related lung cancer is in decline, but the number of cases in never-smokers is rising. Screening tools can detect early lung cancer in smokers (1). However, no comparable approach exists for the latter group, mainly because the biology, risk factors, and genetic mechanisms underlying the disease in these individuals remain elusive. International consortia are investigating the role of alterations in nongerm (somatic) cells and genetic susceptibility in the development of lung cancer in never-smokers. Understanding these biological mechanisms could lead to new therapeutic and screening approaches (2–4). Sometimes, a look at an old problem with different tools can yield unexpected insights. …
摘自《科学》(Science)第393卷 第6817期 · 2026年9月17日,Stephen Chanock。仅引用开头一小段供了解文章,版权归原刊所有,全文请阅读原刊。

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