Connectivity-map unveils Gemcitabine's efficacy in overcoming nelarabine resistance in T-cell acute lymphoblastic leukemia

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ximei Wu , Chunxu Lin , Hui Wang , Jingjing Gao , Suchang chen , Zitao Zhou , Luyong Zhang , Bing Liu , Min Wei
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引用次数: 0

Abstract

Resistance to Nelarabine, the primary FDA-approved therapy for relapsed/refractory T-cell acute lymphoblastic leukemia (T-ALL), is a major obstacle in this high-risk pediatric malignancy. To identify alternative therapies, we have developed two nelarabine-resistant T-ALL cell models and utilized the Connectivity Map (CMap) database to screen for compounds reversing resistance-associated expression profiles., Among the inhibitors screened, gemcitabine emerged as a lead candidate by inhibiting cell proliferation, inducing apoptosis, and suppressing DNA replication in resistant T-ALL cells. RNA sequencing revealed global transcriptomic changes in cells treated with gemcitabine, which were further validated by qRT-PCR. Critically, gemcitabine effectively controlled bone marrow tumor growth in an NSG mouse model with good tolerability. These findings highlight the potential of gemcitabine as a promising therapeutic strategy to overcome nelarabine-resistance in T-ALL.
连接图揭示吉西他滨在t细胞急性淋巴细胞白血病中克服奈拉宾耐药的疗效
耐药奈拉滨是fda批准的治疗复发/难治性t细胞急性淋巴细胞白血病(T-ALL)的主要药物,是治疗这种高危儿童恶性肿瘤的主要障碍。为了确定替代疗法,我们开发了两种耐奈拉宾T-ALL细胞模型,并利用连接图(CMap)数据库筛选逆转耐药相关表达谱的化合物。在筛选的抑制剂中,吉西他滨通过抑制细胞增殖、诱导细胞凋亡和抑制耐药T-ALL细胞的DNA复制而成为主要候选药物。RNA测序揭示了吉西他滨处理细胞的全局转录组变化,并通过qRT-PCR进一步验证了这一点。关键是,吉西他滨在NSG小鼠模型中有效控制骨髓肿瘤生长,具有良好的耐受性。这些发现强调了吉西他滨作为一种有希望的治疗策略来克服T-ALL耐奈拉宾的潜力。
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来源期刊
Biochemical and biophysical research communications
Biochemical and biophysical research communications 生物-生化与分子生物学
CiteScore
6.10
自引率
0.00%
发文量
1400
审稿时长
14 days
期刊介绍: Biochemical and Biophysical Research Communications is the premier international journal devoted to the very rapid dissemination of timely and significant experimental results in diverse fields of biological research. The development of the "Breakthroughs and Views" section brings the minireview format to the journal, and issues often contain collections of special interest manuscripts. BBRC is published weekly (52 issues/year).Research Areas now include: Biochemistry; biophysics; cell biology; developmental biology; immunology ; molecular biology; neurobiology; plant biology and proteomics
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