CES1 与头颈部鳞状细胞癌的顺铂耐药性和不良预后有关。

IF 2 4区 医学 Q3 ONCOLOGY Oncology Research Pub Date : 2024-11-13 eCollection Date: 2024-01-01 DOI:10.32604/or.2024.052244
Chuan Jiang, Chunlei Liu, X I Yao, Jingya Su, Wei Lu, Zhengbo Wei, Ying Xie
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引用次数: 0

摘要

背景:头颈部鳞状细胞癌(HNSCC)是一种全球流行的癌症,其化疗耐药性是治疗效果的一大挑战。常用化疗药物顺铂在预后不良的患者中疗效减弱:方法:利用各种生物信息学数据库研究羧基酯酶1(CES1)基因表达、临床病理特征、患者生存分析和基因功能。建立了HNSCC的类器官模型,并在类器官模型中诱导出耐药的HNSCC。利用 qRT-PCR 和 Western Blot 评估了 CES1 的表达,并通过转录组测序确定了差异标记。利用 shRNA 和慢病毒在 SCC-9 和患者衍生类器官(PDO)细胞中创建了 CES1 的敲除和过表达模型,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 的表达水平与 HNSCC 的预后密切相关。数据表明,CES1的表达与吸烟有重要关系。RNA测序显示,与亲本PDO细胞相比,HNSCC-PDOcis-R细胞中CES1的表达明显增加。随后,我们用 HNSCC-PDO 和 SCC-9 进行了体外研究,发现与 CES1 敲除的细胞相比,CES1 表达的细胞对顺铂的敏感性降低,肿瘤恶性生物学行为更强:结论:观察到的CES1表达与吸烟之间的关联意味着,吸烟可能会通过调控CES1的表达影响HNSCC中以顺铂为基础的化疗的疗效。
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CES1 is associated with cisplatin resistance and poor prognosis of head and neck squamous cell carcinoma.

Background: 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.

Methods: 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.

Results: 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-PDOcis-R cells compared to the parental PDO cells. Subsequently, we performed in vitro 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.

Conclusion: 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.

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来源期刊
Oncology Research
Oncology Research 医学-肿瘤学
CiteScore
4.40
自引率
0.00%
发文量
56
审稿时长
3 months
期刊介绍: Oncology Research Featuring Preclinical and Clincal Cancer Therapeutics publishes research of the highest quality that contributes to an understanding of cancer in areas of molecular biology, cell biology, biochemistry, biophysics, genetics, biology, endocrinology, and immunology, as well as studies on the mechanism of action of carcinogens and therapeutic agents, reports dealing with cancer prevention and epidemiology, and clinical trials delineating effective new therapeutic regimens.
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