紫杉醇
头颈部鳞状细胞癌
下调和上调
癌症研究
微阵列分析技术
微阵列
活力测定
细胞周期
生物
癌症
基因
候选基因
细胞
基因表达
细胞凋亡
头颈部癌
遗传学
作者
Hasan Onur Çağlar,Abdulmelik Aytatli,Neslisah Barlak,Elanur Aydın Karataş,Arzu Tatar,Abdulkadir Şahin,Ömer Faruk Karataş
出处
期刊:Head & neck
[Wiley]
日期:2024-05-16
卷期号:46 (9): 2178-2196
摘要
Abstract Background This study aimed to identify a candidate gene associated with paclitaxel (PTX) resistance and to evaluate functionally its biological role in the PTX‐resistant head and neck squamous cell carcinoma (HNSCC) cell lines and clinical specimens. Methods Microarray data series containing samples of different types of cancers resistant to PTX were analyzed and then a candidate gene associated with PTX resistance was identified using various bioinformatics tools. After the suppression of the target gene expression, changes in cell viability and colony‐forming ability were evaluated in PTX‐resistant FaDu and SCC‐9 cell lines. Results Bioinformatics analyses of upregulated genes in PTX‐resistant cancer cells indicated that OAS3 was associated with PTX resistance. The downregulation of OAS3 expression significantly reduced the viability and colony‐forming capacity of PTX‐resistant SCC‐9 cells by inducing apoptosis and cell cycle arrest at G0/G1 phase. Conclusions The therapeutic targeting of OAS3 may resensitize PTX‐resistant HNSCC cells with high OAS3 expression to PTX treatment.
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