Cho Mildred K, Sankar Pamela
Stanford Center for Biomedical Ethics, 701A Welch Road, Suite 1105, Palo Alto, California 94304, USA.
Nat Genet. 2004 Nov;36(11 Suppl):S8-12. doi: 10.1038/ng1594.
Data on human genetic variation help scientists to understand human origins, susceptibility to illness and genetic causes of disease. Destructive episodes in the history of genetic research make it crucial to consider the ethical and social implications of research in genomics, especially human genetic variation. The analysis of ethical, legal and social implications should be integrated into genetic research, with the participation of scientists who can anticipate and monitor the full range of possible applications of the research from the earliest stages. The design and implementation of research directs the ways in which its results can be used, and data and technology, rather than ethical considerations or social needs, drive the use of science in unintended ways. Here we examine forensic genetics and argue that all geneticists should anticipate the ethical and social issues associated with nonmedical applications of genetic variation research.
关于人类基因变异的数据有助于科学家了解人类起源、疾病易感性和疾病的遗传病因。基因研究历史上的破坏性事件使得考虑基因组学研究,尤其是人类基因变异研究的伦理和社会影响变得至关重要。对伦理、法律和社会影响的分析应融入基因研究中,由能够从最早阶段就预见并监测研究所有可能应用的科学家参与其中。研究的设计和实施决定了其结果的使用方式,而数据和技术而非伦理考量或社会需求以意想不到的方式推动着科学的应用。在此,我们审视法医遗传学,并认为所有遗传学家都应预见与基因变异研究的非医学应用相关的伦理和社会问题。