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OTUD7B表达降低通过非经典核因子κB信号通路与外周T细胞淋巴瘤预后不良相关。

Reduced OTUD7B expression correlates with poor prognosis in PTCL via non-canonical NF-κB.

作者信息

Chen Feng, Qiu Shi, Gui Ailing, Jiang Shiyu, Yan Yichen, Wu Jichuan, Chen Guangliang, Zhu Shun, Liu Yizhen, Xia Zuguang, Yu Baohua, Sun Xiaojian, Gu Juan Jennifer, Wang Lan, Liu Wen, Yang Ling, Zhang Qunling, Zuo Ji

机构信息

Department of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.

Department of Lymphoma, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.

出版信息

Int J Hematol. 2025 Feb;121(2):194-205. doi: 10.1007/s12185-024-03877-y. Epub 2024 Dec 5.

Abstract

Peripheral T cell lymphoma (PTCL) is an aggressive and highly heterogeneous lymphoma with a bleak prognosis, highlighting the urgent need for an effective biomarker to guide therapeutic strategies. Ovarian tumor domain-containing 7B (OTUD7B) has been shown to have a critical function in the progression of cancers. However, the prognostic significance of OTUD7B in PTCL remains unexplored. In this study, we demonstrated for the first time that PTCL patients with low expression of OTUD7B had shorter progression-free survival (PFS) and overall survival (OS). In addition, OTUD7B knockdown promoted chemoresistance to doxorubicin in PTCL cell lines, and led to increased translocation of p52 from the cytoplasm to the nucleus. Inhibition of non-canonical NF-κB partially restored the sensitivity of PTCL cells to doxorubicin. Remarkably, 5-azacytidine and cytarabine upregulated the expression of OTUD7B and exhibited a synergistic anti-lymphoma effect in PTCL. In summary, our study confirmed the prognostic role of OTUD7B in PTCL and the promising therapeutic potential of combining 5-azacytidine or cytarabine and doxorubicin for PTCL treatment.

摘要

外周T细胞淋巴瘤(PTCL)是一种侵袭性强且高度异质性的淋巴瘤,预后不佳,这凸显了迫切需要一种有效的生物标志物来指导治疗策略。含卵巢肿瘤结构域7B(OTUD7B)已被证明在癌症进展中具有关键作用。然而,OTUD7B在PTCL中的预后意义仍未得到探索。在本研究中,我们首次证明OTUD7B低表达的PTCL患者无进展生存期(PFS)和总生存期(OS)较短。此外,敲低OTUD7B可促进PTCL细胞系对阿霉素的化疗耐药性,并导致p52从细胞质向细胞核的转位增加。抑制非经典NF-κB可部分恢复PTCL细胞对阿霉素的敏感性。值得注意的是,5-氮杂胞苷和阿糖胞苷上调了OTUD7B的表达,并在PTCL中表现出协同抗淋巴瘤作用。总之,我们的研究证实了OTUD7B在PTCL中的预后作用,以及联合使用5-氮杂胞苷或阿糖胞苷与阿霉素治疗PTCL的潜在治疗前景。

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