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急性非淋巴细胞白血病:干细胞起源的异质性。

Acute nonlymphocytic leukemia: heterogeneity of stem cell origin.

作者信息

Fialkow P J, Singer J W, Adamson J W, Vaidya K, Dow L W, Ochs J, Moohr J W

出版信息

Blood. 1981 Jun;57(6):1068-73.

PMID:6939452
Abstract

Four patients with acute nonlymphocytic leukemia who were heterozygous for the X-chromosome-linked enzyme glucose-6-phosphate dehydrogenase (G6PD) were studied to determine the numbers and types of progenitor cells in which the disease arose. Both forms of enzyme were found in normal tissues, but the malignant blast cells showed only one G6PD, indicating that the disease was clonal at the time of testing. The observations that normal erythroid cells were present in two young patients at diagnosis and relapse indicate that the clone suppressed expression of normal granulopoiesis but did not prevent normal erythroid differentiation. In contrast to this situation, in two elderly patients, the disease involved stem cells multipotent for granulocytes, red cells, and platelets. These results indicate that acute nonlymphocytic leukemia is heterogeneous. In some patients, the disease is expressed in cells with differentiation restricted to the granulocyte-monocyte pathway; in others, it involves stem cells capable of differentiating to granulocytes-monocytes, platelets, and erythrocytes. This heterogeneity may reflect differences in causation and could have prognostic and therapeutic importance.

摘要

对4名X染色体连锁酶葡萄糖-6-磷酸脱氢酶(G6PD)杂合的急性非淋巴细胞白血病患者进行了研究,以确定其所患疾病起源的祖细胞数量和类型。在正常组织中发现了两种形式的酶,但恶性原始细胞仅显示一种G6PD,这表明在检测时该疾病是克隆性的。两名年轻患者在诊断和复发时存在正常红系细胞的观察结果表明,该克隆抑制了正常粒细胞生成的表达,但并未阻止正常红系分化。与这种情况相反,在两名老年患者中,疾病累及了对粒细胞、红细胞和血小板具有多能性的干细胞。这些结果表明急性非淋巴细胞白血病具有异质性。在一些患者中,疾病在分化仅限于粒细胞-单核细胞途径的细胞中表现;在另一些患者中,它累及能够分化为粒细胞-单核细胞、血小板和红细胞的干细胞。这种异质性可能反映了病因的差异,并且可能具有预后和治疗意义。

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