摘要
2020-02-28封面图描绘的是基因编辑技术就像一把分子剪刀一样被用来编辑DNA。虽然通过基因改良的T细胞颠覆了对癌症的治疗,但它并不能成功地治疗所有的病人。研究人员利用CRISPR从晚期癌症患者的T细胞中切出了3个基因的DNA片段。
CRISPR-Cas9 technology acts as molecular scissors to edit DNA.Genetically modified T cells are:revolutionizing cancer therapy but do not successfully treat all patients.Researchers used CRISPR to cut out sections of DNA on three genes in T cells from patients with advanced cancer.This pioneering therapeutic application of genome editing paves the way for next-generation cell-based therapies for human disease.
出处
《中国科技教育》
2020年第4期49-49,共1页
China Science & Technology Education
