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癌基因、分子医学与骨髓移植。

Oncogenes, molecular medicine, and bone marrow transplantation.

作者信息

Hijiya N, Gewirtz A M

机构信息

Department of Pathology, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

J Hematother. 1992 Winter;1(4):369-78. doi: 10.1089/scd.1.1992.1.369.

Abstract

Retroviruses are known to carry specific genes that are likely to be responsible for induction of the malignant phenotype in the cells they infect. These genes, termed viral oncogenes (v-onc), have subsequently been shown to be derived from highly conserved, normal cellular genes commonly referred to as proto-oncogenes (c-onc). Proto-oncogenes are thought to be intimately involved in the processes of cell proliferation and differentiation. Therefore, any c-onc amplification, mutation, structural alteration, or change in transcriptional regulation might lead to, or be associated with, induction of a malignant phenotype. Targeted disruption of these genes may therefore be of therapeutic value. We discuss the role of antisense DNA in carrying out such therapy.

摘要

已知逆转录病毒携带特定基因,这些基因可能是其所感染细胞中恶性表型诱导的原因。这些基因被称为病毒癌基因(v-onc),随后被证明源自高度保守的正常细胞基因,通常称为原癌基因(c-onc)。原癌基因被认为与细胞增殖和分化过程密切相关。因此,任何c-onc的扩增、突变、结构改变或转录调控变化都可能导致或与恶性表型的诱导相关。因此,对这些基因进行靶向破坏可能具有治疗价值。我们讨论了反义DNA在实施这种治疗中的作用。

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