SRY-related HMG-box 5 enhances chemosensitivity in esophageal squamous cell carcinoma through toll-like receptor 4/NOD-like receptor family pyrin domain containing 3-mediated pyroptosis.

IF 4.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Wenbin Hu, Jiaming Zhao, Qihao Wang, Mingming Deng, Binjun He, Xiaoyan Wang
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引用次数: 0

Abstract

Despite established roles in multiple cancers, the specific function and molecular mechanism of SRY-related HMG-box 5 (SOX5) remain elusive in esophageal squamous cell carcinoma (ESCC). SOX5 expression in ESCC tissues, its correlation with prognosis, and its relationship with toll-like receptor 4 (TLR4) and NOD-like receptor family pyrin domain containing 3 (NLRP3) were assessed with bioinformatic methods. Expression of SOX5 and TLR4 in ESCC cells was detected by quantitative reverse transcription polymerase chain reaction. In SOX5-overexpressing or TLR4-knockdown ESCC cells, cell death was evaluated by propidium iodide staining, migration and invasion were detected using Transwell assays, cell proliferation was assessed by colony formation assay, pyroptosis was observed using an optical microscope and confirmed using Annexin V/7-aminoactinomycin D staining, the binding of SOX5 to the TLR4 promoter was confirmed by chromatin immunoprecipitation assay, and the expression of key pyroptosis pathway proteins (Gasdermin D, Gasdermin D-N, cleaved Caspase-1 (c-CASP1), and NLRP3) was analyzed by Western blot. SOX5 downregulation in ESCC tissues and cells was observed and correlated with shorter survival in patients with ESCC. SOX5 expression positively correlated with the key pyroptosis pathway genes TLR4 and NLRP3. SOX5 overexpression promoted ESCC cell pyroptosis and enhanced sensitivity to cisplatin (DDP). Mechanistically, SOX5 interacted with the TLR4 promoter and upregulated key pyroptosis pathway proteins; TLR4 knockdown reduced the enhanced pyroptosis and DDP sensitivity observed in SOX5-overexpressing cells. SOX5 enhances DDP sensitivity in ESCC by mediating TLR4/NLRP3 expression to promote cell pyroptosis, providing novel insights for ESCC treatment. SIGNIFICANCE STATEMENT: SRY-related HMG-box 5 function in esophageal squamous cell carcinoma was uncovered. SRY-related HMG-box 5 regulated toll-like receptor 4/NOD-like receptor family pyrin domain containing 3 to mediate pyroptosis.

sry相关的HMG-box 5通过toll样受体4/ nod样受体家族pyrin结构域包含3介导的焦亡增强食管鳞状细胞癌的化疗敏感性。
尽管在多种癌症中有明确的作用,但sry相关的HMG-box 5 (SOX5)在食管鳞状细胞癌(ESCC)中的具体功能和分子机制尚不清楚。采用生物信息学方法评估SOX5在ESCC组织中的表达、与预后的相关性以及与toll样受体4 (TLR4)、nod样受体家族pyrin domain containing 3 (NLRP3)的关系。采用定量逆转录聚合酶链反应检测ESCC细胞中SOX5和TLR4的表达。在SOX5过表达或TLR4低表达的ESCC细胞中,碘化丙酸染色评估细胞死亡,Transwell法检测细胞迁移和侵袭,集落形成法评估细胞增殖,光学显微镜观察细胞焦亡,Annexin V/7-氨基放射线霉素D染色证实细胞焦亡,染色质免疫沉淀法证实SOX5与TLR4启动子结合。Western blot分析焦亡通路关键蛋白Gasdermin D、Gasdermin D- n、cleaved Caspase-1 (c-CASP1)、NLRP3的表达。在ESCC患者的组织和细胞中观察到SOX5下调,并与较短的生存期相关。SOX5的表达与焦亡通路关键基因TLR4、NLRP3呈正相关。SOX5过表达促进ESCC细胞焦亡,增强对顺铂的敏感性。机制上,SOX5与TLR4启动子相互作用,上调关键的焦亡途径蛋白;TLR4敲除降低了sox5过表达细胞中观察到的焦亡增强和DDP敏感性。SOX5通过介导TLR4/NLRP3表达促进ESCC细胞焦亡,从而增强DDP在ESCC中的敏感性,为ESCC的治疗提供了新的思路。意义声明:发现食管鳞状细胞癌中sry相关的HMG-box - 5功能。sry相关HMG-box 5调节toll样受体4/ nod样受体家族pyrin结构域3介导焦亡。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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