Unknown

Dataset Information

0

3-Ketodihydrosphingosine reductase maintains ER homeostasis and unfolded protein response in leukemia.


ABSTRACT: Sphingolipids and their metabolic pathways have been implicated in disease development and therapeutic response; however, the detailed mechanisms remain unclear. Using a sphingolipid network focused CRISPR/Cas9 library screen, we identified an endoplasmic reticulum (ER) enzyme, 3-Ketodihydrosphingosine reductase (KDSR), to be essential for leukemia cell maintenance. Loss of KDSR led to apoptosis, cell cycle arrest, and aberrant ER structure. Transcriptomic analysis revealed the indispensable role of KDSR in maintaining the unfolded protein response (UPR) in ER. High-density CRISPR tiling scan and sphingolipid mass spectrometry pinpointed the critical role of KDSR's catalytic function in leukemia. Mechanistically, depletion of KDSR resulted in accumulated 3-ketodihydrosphingosine (KDS) and dysregulated UPR checkpoint proteins PERK, ATF6, and ATF4. Finally, our study revealed the synergism between KDSR suppression and pharmacologically induced ER-stress, underscoring a therapeutic potential of combinatorial targeting sphingolipid metabolism and ER homeostasis in leukemia treatment.

SUBMITTER: Liu Q 

PROVIDER: S-EPMC8732298 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

3-Ketodihydrosphingosine reductase maintains ER homeostasis and unfolded protein response in leukemia.

Liu Qiao Q   Chan Anthony K N AKN   Chang Wen-Han WH   Yang Lu L   Pokharel Sheela Pangeni SP   Miyashita Kazuya K   Mattson Nicole N   Xu Xiaobao X   Li Mingli M   Lu Wei W   Lin Ren-Jang RJ   Wang Shao-Yuan SY   Chen Chun-Wei CW  

Leukemia 20210809 1


Sphingolipids and their metabolic pathways have been implicated in disease development and therapeutic response; however, the detailed mechanisms remain unclear. Using a sphingolipid network focused CRISPR/Cas9 library screen, we identified an endoplasmic reticulum (ER) enzyme, 3-Ketodihydrosphingosine reductase (KDSR), to be essential for leukemia cell maintenance. Loss of KDSR led to apoptosis, cell cycle arrest, and aberrant ER structure. Transcriptomic analysis revealed the indispensable rol  ...[more]

Similar Datasets

| S-EPMC11626163 | biostudies-literature
| S-EPMC6094449 | biostudies-literature
| S-EPMC6459409 | biostudies-literature
| S-EPMC10204200 | biostudies-literature
| S-EPMC10629814 | biostudies-literature
2021-07-24 | GSE167688 | GEO
| S-EPMC4653219 | biostudies-literature
| S-EPMC3354055 | biostudies-literature
| S-EPMC3094110 | biostudies-literature
| S-EPMC11234256 | biostudies-literature