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raf和myc癌基因对造血细胞的转化:谱系定向的新视角。

Transformation of hemopoietic cells by raf and myc oncogenes: a new perspective on lineage commitment.

作者信息

Klinken S P

机构信息

Department of Biochemistry, University of Western Australia, Nedlands.

出版信息

Cancer Cells. 1991 Oct;3(10):373-82.

PMID:1777358
Abstract

The effects of the raf and myc oncogenes on murine hemopoietic cells are quite distinct. The raf-1 gene, which encodes a serine/threonine kinase that is involved in signal transduction, preferentially transforms erythroid cells, whereas myc, which encodes a DNA-binding protein, induces lymphoid and myeloid neoplasms. Together, raf and myc form a potent leukemogenic combination and they act synergistically to transform cells from all hemopoietic lineages. Strikingly, the expression of exogenous raf and myc in lymphoid and erythroid cells enables these cells to change lineages and become myeloid cells, an observation that raises interesting questions concerning commitment to specific lineages.

摘要

raf和myc癌基因对小鼠造血细胞的影响截然不同。raf - 1基因编码一种参与信号转导的丝氨酸/苏氨酸激酶,它优先转化红系细胞,而编码DNA结合蛋白的myc则诱导淋巴系和髓系肿瘤。raf和myc共同形成一种强大的致白血病组合,它们协同作用以转化所有造血谱系的细胞。令人惊讶的是,在淋巴系和红系细胞中表达外源性raf和myc能使这些细胞改变谱系并成为髓系细胞,这一观察结果引发了关于特定谱系定向的有趣问题。

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