| Literature DB >> 24937459 |
Cai-Wen Duan1, Jun Shi2, Jing Chen3, Bo Wang1, Ye-Hua Yu2, Xia Qin3, Xiang-Cheng Zhou1, Yi-Jun Cai1, Zuo-Qing Li1, Fang Zhang3, Min-Zhi Yin3, Ying Tao2, Jian-Qing Mi4, Lin-Heng Li5, Tariq Enver6, Guo-Qiang Chen7, Deng-Li Hong8.
Abstract
Residence of cancer-propagating cells (CPCs) within preferential microenvironmental niches has a major part in evading therapy. However, the nature of niches involved and the mechanisms protecting CPCs remain largely unknown. We addressed these issues in mouse transplantation models of acute lymphoblastic leukemia (ALL). When the engrafted leukemic cells substantially damaged adjacent microenvironment in the bone marrow (BM), after chemotherapy small foci of CPCs were retained, surrounded by sheaths of supporting cells that comprise a protective niche. We investigated patients' BM biopsies and found evidence of a similar process in patients receiving induction therapy. The efficacy of chemotherapy was enhanced by interfering with the niche formation or function. We therefore identified a therapy-induced niche that protects CPCs.Entities:
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Year: 2014 PMID: 24937459 DOI: 10.1016/j.ccr.2014.04.015
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743