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一个将 BCR 与 NAD 生物合成酶 NAMPT 联系起来的分子回路是 Richter 综合征中的一个可行靶点。

A molecular circuit linking the BCR to the NAD biosynthetic enzyme NAMPT is an actionable target in Richter syndrome.

机构信息

Laboratory of Functional Genomics, Department of Medical Sciences, University of Turin, Turin, Italy.

Department of Molecular Biotechnologies and Health Science, University of Turin, Turin, Italy.

出版信息

Blood Adv. 2024 Apr 23;8(8):1920-1933. doi: 10.1182/bloodadvances.2023011690.

Abstract

This works defines, to the best of our knowledge, for the first time a molecular circuit connecting nicotinamide mononucleoside phosphoribosyl transferase (NAMPT) activity to the B-cell receptor (BCR) pathway. Using 4 distinct xenograft models derived from patients with Richter syndrome (RS-PDX), we show that BCR cross-linking results in transcriptional activation of the nicotinamide adenine dinucleotide (NAD) biosynthetic enzyme NAMPT, with increased protein expression, in turn, positively affecting global cellular NAD levels and sirtuins activity. NAMPT blockade, by using the novel OT-82 inhibitor in combination with either BTK or PI3K inhibitors (BTKi or PI3Ki), induces rapid and potent apoptotic responses in all 4 models, independently of their mutational profile and the expression of the other NAD biosynthetic enzymes, including nicotinate phosphoribosyltransferase. The connecting link in the circuit is represented by AKT that is both tyrosine- and serine-phosphorylated by PI3K and deacetylated by sirtuin 1 and 2 to obtain full kinase activation. Acetylation (ie, inhibition) of AKT after OT-82 administration was shown by 2-dimensional gel electrophoresis and immunoprecipitation. Consistently, pharmacological inhibition or silencing of sirtuin 1 and 2 impairs AKT activation and induces apoptosis of RS cells in combination with PI3Ki or BTKi. Lastly, treatment of RS-PDX mice with the combination of PI3Ki and OT-82 results in significant inhibition of tumor growth, with evidence of in vivo activation of apoptosis. Collectively, these data highlight a novel application for NAMPT inhibitors in combination with BTKi or PI3Ki in aggressive lymphomas.

摘要

本研究首次定义了一个将烟酰胺单核苷酸磷酸核糖转移酶(NAMPT)活性与 B 细胞受体(BCR)途径连接起来的分子通路。使用源自 Richter 综合征(RS)患者的 4 种不同的异种移植模型,我们发现 BCR 交联导致烟酰胺腺嘌呤二核苷酸(NAD)生物合成酶 NAMPT 的转录激活,随之而来的是蛋白表达增加,进而正向影响细胞内 NAD 水平和去乙酰化酶(Sirtuins)活性。新型 OT-82 抑制剂联合 BTK 或 PI3K 抑制剂(BTKi 或 PI3Ki)抑制 NAMPT,可在所有 4 种模型中诱导迅速而有效的凋亡反应,而与它们的突变状态和其他 NAD 生物合成酶的表达无关,包括烟酸磷酸核糖基转移酶。该通路中的连接环节是 AKT,它被 PI3K 酪氨酸和丝氨酸磷酸化,并被 Sirtuin 1 和 2 去乙酰化以获得完全的激酶激活。OT-82 给药后 AKT 的乙酰化(即抑制)通过二维凝胶电泳和免疫沉淀得到证实。一致地,Sirtuin 1 和 2 的药理学抑制或沉默会损害 AKT 激活,并与 PI3Ki 或 BTKi 联合诱导 RS 细胞凋亡。最后,PI3Ki 和 OT-82 的联合治疗可显著抑制 RS-PDX 小鼠的肿瘤生长,并在体内证实了凋亡的激活。综上所述,这些数据突出了 NAMPT 抑制剂联合 BTKi 或 PI3Ki 在侵袭性淋巴瘤中的新应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f24/11021907/59beaf4ca435/BLOODA_ADV-2023-011690-ga1.jpg

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