Wogonin induces mitochondrial apoptosis and synergizes with venetoclax in diffuse large B-cell lymphoma

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ye Lin , Xia Jiang , Mengting Zhao , Youhong Li , Lili Jin , Sumeng Xiang , Renzhi Pei , Ying Lu , Lei Jiang
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Abstract

Diffuse large B-cell lymphoma (DLBCL) is among the most aggressive hematological malignancies and patients are commonly treated with combinatorial immunochemotherapies such as R-CHOP. Till now, the prognoses are still variable and unsatisfactory, depending on the molecular subtype and the treatment response. Developing effective and tolerable new agents is always urgently needed, and compounds from a natural source have gained increasing attentions. Wogonin is an active flavonoid extracted from the traditional Chinese herbal medicine Scutellaria baicalensis Georgi and has shown extensive antitumor potentials. However, the therapeutic effect of wogonin on DLBCL remains unknown. Here, we found that treatment with wogonin dose- and time-dependently reduced the viability in a panel of established DLBCL cell lines. The cytotoxicity of wogonin was mediated through apoptosis induction, along with the loss of mitochondrial membrane potential and the downregulation of BCL-2, MCL-1, and BCL-xL. In terms of the mechanism, wogonin inhibited the PI3K and MAPK pathways, as evidenced by the clear decline in the phosphorylation of AKT, GSK3β, S6, ERK, and P38. Furthermore, the combination of wogonin and the BCL-2 inhibitor venetoclax elicited synergistically enhanced killing effect on DLBCL cells regardless of their molecular subtypes. Finally, administration of wogonin significantly impeded the progression of the DLBCL tumor in a xenograft animal model without obvious side effects. Taken together, the present study suggests a promising potential of wogonin in the treatment of DLBCL patients either as monotherapy or an adjuvant for venetoclax-based combinations.

Abstract Image

Wogonin 可诱导弥漫大 B 细胞淋巴瘤线粒体凋亡并与 Venetoclax 协同作用
弥漫大B细胞淋巴瘤(DLBCL)是侵袭性最强的血液恶性肿瘤之一,患者通常接受R-CHOP等联合免疫疗法治疗。迄今为止,根据分子亚型和治疗反应的不同,预后仍不尽人意。开发有效且可耐受的新药一直是当务之急,而来自天然的化合物越来越受到人们的关注。五加皮苷是从传统中药黄芩中提取的一种活性黄酮类化合物,具有广泛的抗肿瘤潜力。然而,五加皮苷对DLBCL的治疗效果仍然未知。在这里,我们发现沃格宁在剂量和时间上依赖性地降低了一组已建立的 DLBCL 细胞系的存活率。沃戈宁的细胞毒性是通过诱导细胞凋亡、线粒体膜电位丧失以及下调 BCL-2、MCL-1 和 BCL-xL 来介导的。在机制方面,沃格宁抑制了 PI3K 和 MAPK 通路,这表现在 AKT、GSK3β、S6、ERK 和 P38 的磷酸化明显下降。此外,沃格宁与BCL-2抑制剂venetoclax联用可协同增强对DLBCL细胞的杀伤作用,而不论其分子亚型如何。最后,在无明显副作用的异种移植动物模型中,服用沃戈宁能显著阻碍DLBCL肿瘤的进展。综上所述,本研究表明沃戈宁具有治疗DLBCL患者的巨大潜力,既可以作为单一疗法,也可以作为基于venetoclax的联合疗法的辅助疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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