慢性髓性白血病的干细胞持久性。

Leukemia supplements Pub Date : 2012-08-01 Epub Date: 2012-08-09 DOI:10.1038/leusup.2012.24
M Deininger
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引用次数: 5

摘要

BCR-ABL的酪氨酸激酶抑制剂(TKIs)已将慢性髓性白血病(CML)从一种致命疾病转变为一种慢性疾病。不幸的是,越来越多的证据表明TKI不能治愈,因为CML干细胞对BCR-ABL不上瘾,尽管TKI治疗仍持续存在。仔细观察,这并不奇怪,因为它反映了CML发病机制的基本原理。根除CML干细胞的策略很可能基于通过并行抑制BCR-ABL和其他关键途径的合成致死性。
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Stem cell persistence in chronic myeloid leukemia.

Tyrosine kinase inhibitors (TKIs) of BCR-ABL have turned chronic myeloid leukemia (CML) from a deadly disease into a chronic ailment. Unfortunately, evidence is accumulating that TKIs are not curative, since CML stem cells are not addicted to BCR-ABL, and persist despite TKI therapy. On closer view this is not surprising, as it reflects fundamental principles of CML pathogenesis. Strategies to eradicate CML stem cells will most likely be based on synthetic lethality though parallel inhibition of BCR-ABL and other critical pathways.

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Abstracts from the 2nd International Norges Teknisk-Naturvitenskapelige Universitet (NTNU) Symposium: Day 1—Immunotherapy and Hematology Altered microenvironmental regulation of CML stem cells. Harnessing alloreactivity to achieve anti-leukemic responses. Reconsidering marrow stem cell cycle status: insights into an actively cycling hematopoietic stem cell population. Targeting leukemia stem cells with HDAC inhibitors and modulators of the DNA damage response.
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