Key Laboratory of Early Prevention and Treatment for Regional High Frequency Tumor (Guangxi Medical University), Ministry ofEducation, Nanning, 530000, China.
Life Sciences Institute, Guangxi Medical University, Nanning, 530000, China.
Oncol Res. 2024 Nov 13;32(12):1935-1948. doi: 10.32604/or.2024.052244. eCollection 2024.
Head and neck squamous cell carcinoma (HNSCC) is a prevalent form of cancer globally, with chemoresistance posing a major challenge in treatment outcomes. The efficacy of the commonly used chemotherapeutic agent, cisplatin, is diminished in patients with poor prognoses.
Various bioinformatics databases were utilized to examine Carboxylesterase 1 (CES1) gene expression, clinicopathologic features, patient survival analysis, and gene function. An organoid model of HNSCC was established, along with the induction of drug-resistant HNSCC in the organoid model. CES1 expression was assessed using qRT-PCR and Western Blot, and differential markers were identified through transcriptome sequencing. Knockdown and overexpression models of CES1 were created in SCC-9 and patient-derived organoid (PDO) cells using shRNA and lentivirus to investigate the tumor biology and cisplatin resistance associated with CES1.
Research in bioinformatics has uncovered a strong correlation between the expression level of CES1 and the prognosis of HNSCC. The data suggests a significant link between CES1 expression and tobacco smoking. RNA-sequencing revealed a notable increase in CES1 expression in HNSCC-PDO cells compared to the parental PDO cells. Subsequently, we performed studies by HNSCC-PDO and SCC-9 and found that CES1-overexpressing cells exhibited reduced sensitivity to cisplatin and stronger tumor malignant biological behavior compared with CES1-knockdown cells.
The observed association between CES1 expression and tobacco smoking implies a potential influence of smoking on the efficacy of cisplatin-based chemotherapy in HNSCC through the regulation of CES1 expression.
头颈部鳞状细胞癌(HNSCC)是一种全球普遍存在的癌症,化疗耐药性是治疗效果的主要挑战。常用化疗药物顺铂在预后不良的患者中疗效降低。
利用各种生物信息学数据库研究羧酸酯酶 1(CES1)基因表达、临床病理特征、患者生存分析和基因功能。建立 HNSCC 类器官模型,并在类器官模型中诱导化疗耐药性 HNSCC。使用 qRT-PCR 和 Western Blot 评估 CES1 表达,并通过转录组测序鉴定差异标记物。使用 shRNA 和慢病毒在 SCC-9 和患者来源的类器官(PDO)细胞中创建 CES1 的敲低和过表达模型,以研究与 CES1 相关的肿瘤生物学和顺铂耐药性。
生物信息学研究发现 CES1 表达水平与 HNSCC 预后之间存在很强的相关性。数据表明 CES1 表达与吸烟之间存在显著关联。RNA-seq 显示 HNSCC-PDO 细胞中 CES1 表达明显高于亲本 PDO 细胞。随后,我们通过 HNSCC-PDO 和 SCC-9 进行了研究,发现与 CES1 敲低细胞相比,CES1 过表达细胞对顺铂的敏感性降低,肿瘤恶性生物学行为增强。
观察到 CES1 表达与吸烟之间的关联表明,吸烟可能通过调节 CES1 表达影响 HNSCC 中基于顺铂的化疗的疗效。