SGLT-2抑制剂有效抑制惰性型成人t细胞白血病/淋巴瘤的侵袭性转化:对糖尿病相关血液恶性肿瘤治疗的独特见解

IF 1.2
EJHaem Pub Date : 2025-09-08 DOI:10.1002/jha2.70109
Kazuho Morichika, Keita Tamaki, Takuya Fukushima, Hiroaki Masuzaki
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引用次数: 0

摘要

我们之前报道过钠-葡萄糖共转运蛋白2 (SGLT-2)在成人t细胞白血病(ATL)细胞中异位过表达,尤其是侵袭型和惰性型,广泛使用的抗糖尿病SGLT-2抑制剂(SGLT-2i)显著降低白血病细胞的增殖。方法我们进行了10年的回顾性分析,以观察SGLT-2i是否能预防伴有糖尿病的惰性ATL患者的侵袭性转化。我们还评估了SGLT-2基因启动子区域的核小体占用情况,以探索表观遗传修饰在这种异位过表达中的可能参与。结果在伴有糖尿病的无痛ATL患者中,非SGLT-2i治疗组的累积进展率为71%,而SGLT-2i治疗组没有患者发生侵袭性转化。ATL细胞SGLT-2基因启动子区核小体占用率明显下降。结论SGLT-2i有利于预防惰性ATL的恶化转化。试验注册作者确认,本研究和本文未要求临床试验注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SGLT-2 Inhibitors Are Potent to Suppress Aggressive Transformation From Indolent Type of Adult T-Cell Leukemia/Lymphoma: Unique Insight Into Therapeutics for Diabetes-Related Hematological Malignancy

SGLT-2 Inhibitors Are Potent to Suppress Aggressive Transformation From Indolent Type of Adult T-Cell Leukemia/Lymphoma: Unique Insight Into Therapeutics for Diabetes-Related Hematological Malignancy

Introduction

We previously reported that sodium-glucose co-transporter 2 (SGLT-2) was ectopically overexpressed in adult T-cell leukemia (ATL) cells notably in aggressive type but in indolent type, and widely-used anti-diabetic SGLT-2 inhibitors (SGLT-2i) considerably attenuated proliferation of leukemic cells.

Methods

We performed retrospective analyses for 10 years to see whether SGLT-2i would prevent aggressive transformation in patients with indolent type ATL accompanied by diabetes. Nucleosome occupancy in the promotor region of the SGLT-2 gene was also assessed to explore the possible involvement of epigenetic modification in such an ectopic overexpression.

Results

In patients of indolent ATL with diabetes, the cumulative progression rate in the non-SGLT-2i-treated group was 71%, while no patients developed aggressive transformation in the SGLT-2i treated group. ATL cells showed an apparent trend to decrease nucleosome occupancy in the promotor region of the SGLT-2 gene.

Conclusion

Our data suggest that SGLT-2i is advantageous for preventing aggravative transformation in indolent ATL.

Trial Registration

Authors confirmed that clinical trial registration was not requested for the present study and this manuscript.

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