ZDHHC9介导的Bip/GRP78 S-棕榈酰化抑制折叠蛋白反应并促进膀胱癌的进展。

IF 9.1 1区 医学 Q1 ONCOLOGY
Weiquan Li , Jingchong Liu , Tiexi Yu , Feiyi Lu , Qi Miao , Xiangui Meng , Wen Xiao , Hongmei Yang , Xiaoping Zhang
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引用次数: 0

摘要

最近的研究突出表明,棕榈酰化这种新型蛋白质翻译后修饰是导致肿瘤发生和耐药性的各种信号通路中的关键角色。尽管如此,人们对棕榈酰化在膀胱癌(BCa)发展中的作用仍然了解不足。在这项研究中,ZDHHC9成为膀胱癌中显著上调的癌基因。在功能上,ZDHHC9敲除可明显抑制肿瘤增殖,促进肿瘤细胞凋亡,并增强吉西他滨(GEM)和顺铂(CDDP)的疗效。研究发现,SP1能转录激活ZDHHC9的表达。ZDHHC9 随后与 Bip 蛋白结合,并在半胱氨酸 420(Cys420)处对其进行棕榈酰化,从而抑制了未折叠蛋白反应(UPR)。Cys420处的棕榈酰化增强了Bip蛋白的稳定性,并保持了其在内质网(ER)中的定位。ZDHHC9可能成为BCa的一个新的治疗靶点,也可能有助于GEM和CDDP的联合治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ZDHHC9-mediated Bip/GRP78 S-palmitoylation inhibits unfolded protein response and promotes bladder cancer progression

ZDHHC9-mediated Bip/GRP78 S-palmitoylation inhibits unfolded protein response and promotes bladder cancer progression

Recent studies have highlighted palmitoylation, a novel protein post-translational modification, as a key player in various signaling pathways that contribute to tumorigenesis and drug resistance. Despite this, its role in bladder cancer (BCa) development remains inadequately understood. In this study, ZDHHC9 emerged as a significantly upregulated oncogene in BCa. Functionally, ZDHHC9 knockdown markedly inhibited tumor proliferation, promoted tumor cell apoptosis, and enhanced the efficacy of gemcitabine (GEM) and cisplatin (CDDP). Mechanistically, SP1 was found to transcriptionally activate ZDHHC9 expression. ZDHHC9 subsequently bound to and palmitoylated the Bip protein at cysteine 420 (Cys420), thereby inhibiting the unfolded protein response (UPR). This palmitoylation at Cys420 enhanced Bip's protein stability and preserved its localization within the endoplasmic reticulum (ER). ZDHHC9 might become a novel therapeutic target for BCa and could also contribute to combination therapy with GEM and CDDP.

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来源期刊
Cancer letters
Cancer letters 医学-肿瘤学
CiteScore
17.70
自引率
2.10%
发文量
427
审稿时长
15 days
期刊介绍: Cancer Letters is a reputable international journal that serves as a platform for significant and original contributions in cancer research. The journal welcomes both full-length articles and Mini Reviews in the wide-ranging field of basic and translational oncology. Furthermore, it frequently presents Special Issues that shed light on current and topical areas in cancer research. Cancer Letters is highly interested in various fundamental aspects that can cater to a diverse readership. These areas include the molecular genetics and cell biology of cancer, radiation biology, molecular pathology, hormones and cancer, viral oncology, metastasis, and chemoprevention. The journal actively focuses on experimental therapeutics, particularly the advancement of targeted therapies for personalized cancer medicine, such as metronomic chemotherapy. By publishing groundbreaking research and promoting advancements in cancer treatments, Cancer Letters aims to actively contribute to the fight against cancer and the improvement of patient outcomes.
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