| Literature DB >> 30784597 |
Wenbin Zhong1, Mengyang Xu2, Chanjuan Li2, Biying Zhu1, Xiuye Cao1, Dan Li1, Huanzhao Chen1, Chunxiu Hu3, Rong Li4, Chengwei Luo5, Guoping Pan1, Wenqiang Zhang1, Chaofeng Lai1, Tong Wang1, Xin Du5, Hong Chen6, Guowang Xu3, Vesa M Olkkonen7, Pingsheng Lei8, Jun Xu2, Daoguang Yan9.
Abstract
Leukemia stem cells (LSCs) are a rare subpopulation of abnormal hematopoietic stem cells (HSCs) that propagates leukemia and are responsible for the high frequency of relapse in therapies. Detailed insights into LSCs' survival will facilitate the identification of targets for therapeutic approaches. Here, we develop an inhibitor, LYZ-81, which targets ORP4L with high affinity and specificity and selectively eradicates LCSs in vitro and in vivo. ORP4L is expressed in LSCs but not in normal HSCs and is essential for LSC bioenergetics and survival. It extracts PIP2 from the plasma membrane and presents it to PLCβ3, enabling IP3 generation and subsequent Ca2+-dependent bioenergetics. LYZ-81 binds ORP4L competitively with PIP2 and blocks PIP2 hydrolysis, resulting in defective Ca2+ signaling. The results provide evidence that LSCs can be eradicated through the inhibition of ORP4L by LYZ-81, which may serve as a starting point of drug development for the elimination of LSCs to eventually cure leukemia.Entities:
Keywords: Ca(2+) signaling; OSBP-related protein 4L; PIP(2) hydrolysis; energy metabolism; leukemia stem cell; therapy
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Year: 2019 PMID: 30784597 DOI: 10.1016/j.celrep.2019.01.082
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423