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Pharmacological targeting PIKfyve and tubulin as an effective treatment strategy for double-hit lymphoma.


ABSTRACT: Double-hit lymphoma is one of the most aggressive and refractory lymphoma subtypes with recurrent genetic abnormalities of MYC and BCL-2 or BCL6 rearrangement, leading to a poor prognosis in the present clinical practice. Therefore, new therapeutic strategies for eliminating double-hit lymphomas are urgently needed. Here, we reported that HZX-02-059, a novel PIKfyve and tubulin dual-target inhibitor, showed a highly cytotoxic activity against double-hit lymphoma cell lines in vitro and in vivo through a noncanonical caspase-independent cell death, methuosis. Mechanistically, the cytotoxicity triggered by HZX-02-059 was contributed to the PIKfyve/TFEB axis-induced cell death of methuosis, as well as the inhibition of tubulin and mTOR/Myc axis-induced cell cycle arrest. In summary, the present findings suggest that HZX-02-059 represents a good starting point for developing targeted therapeutics against double-hit lymphomas.

SUBMITTER: Feng L 

PROVIDER: S-EPMC8799717 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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Pharmacological targeting PIKfyve and tubulin as an effective treatment strategy for double-hit lymphoma.

Feng Liying L   Chen Kai K   Huang Wei W   Jiang Yuelong Y   Sun Xihuan X   Zhou Yong Y   Li Li L   Li Yin Y   Deng Xianming X   Xu Bing B  

Cell death discovery 20220128 1


Double-hit lymphoma is one of the most aggressive and refractory lymphoma subtypes with recurrent genetic abnormalities of MYC and BCL-2 or BCL6 rearrangement, leading to a poor prognosis in the present clinical practice. Therefore, new therapeutic strategies for eliminating double-hit lymphomas are urgently needed. Here, we reported that HZX-02-059, a novel PIKfyve and tubulin dual-target inhibitor, showed a highly cytotoxic activity against double-hit lymphoma cell lines in vitro and in vivo t  ...[more]

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