白血病的细胞和分子环境。

Blood cells Pub Date : 1993-01-01
L Sachs
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引用次数: 0

摘要

识别正常的生存能力、生长和分化诱导细胞因子、产生细胞因子的细胞,以及细胞因子在正常发育中的相互作用,使得识别正常发育的细胞和分子基础以及导致白血病的发育程序中的变化成为可能。当正常细胞转变为白血病细胞时,恶性表型可以通过各种方式再次被抑制。关于正常髓系造血细胞生长、分化和凋亡的分子控制,髓系白血病正常发育程序的变化,以及髓系白血病恶性肿瘤的抑制的研究结果表明(A)无论肿瘤细胞是否发生遗传改变,恶性肿瘤都可以被抑制;(B)通过诱导分化来抑制恶性肿瘤,并不需要恢复所有的正常对照。(C)可以通过诱导分化和细胞凋亡来阻止细胞增殖,从而绕过导致恶性肿瘤的遗传异常,并消除其影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The cellular and molecular environment in leukemia.

Identification of normal viability-, growth-, and differentiation-inducing cytokines, the cells that produce them, and how cytokines interact in normal development, has made it possible to identify the cellular and molecular basis of normal development and changes in the developmental program that result in leukemia. When normal cells have been changed into leukemic cells, the malignant phenotype can again be suppressed in various ways. Results on the molecular control of growth, differentiation, and apoptosis in normal myeloid hematopoietic cells, changes in the normal developmental program in myeloid leukemia, and the suppression of malignancy in myeloid leukemia, have shown that (A) malignancy can be suppressed either with or without genetic changes in the tumor cells, (B) suppression of malignancy by inducing differentiation does not have to restore all the normal controls, and (C) genetic abnormalities which give rise to malignancy can be bypassed and their effects nullified by inducing differentiation and apoptosis which stop cells from multiplying.

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