Cho Sang Yeon, Kang Nam Sook
Graduate School of New Drug Discovery and Development, Chungnam National University, Daejeon 34134, Republic of Korea.
CHOMEDICINE Inc., TIPS Town, Chungnam National University, Daejeon 34135, Republic of Korea.
Cancers (Basel). 2024 Sep 22;16(18):3226. doi: 10.3390/cancers16183226.
: Head and neck squamous cell carcinoma (HNSC) is the most prevalent cancer in the head and neck region, originating from the mucosal epithelium of the oral cavity, pharynx, and larynx. The solute carrier (SLC) transporter superfamily, consisting of over 400 proteins across 65 families, plays a crucial role in cellular functions and presents promising targets in precision oncology. This study aims to analyze the expression of SLC transporters in HNSC and their potential as biomarkers and therapeutic targets. : We leveraged mRNA and protein expression data from The Cancer Genome Atlas (TCGA) and The Human Protein Atlas (HPA) to examine SLC transporter expression in HNSC. Gene Set Enrichment Analysis (GSEA) was conducted to assess the involvement of SLC transporters in various oncogenic pathways. : Significant upregulation of SLC transporters was observed in tumor tissues compared to normal tissues, with notable increases in SLC16A3, SLC53A1, SLC25A32, and SLC2A3. This upregulation correlated with poorer overall survival (OS) and disease-specific survival (DSS). GSEA revealed that these transporters are significantly involved in critical oncogenic pathways, including epithelial-mesenchymal transition (EMT), angiogenesis, and hypoxia, which are vital for cancer progression and metastasis. : The study identifies SLC transporters as potential biomarkers and therapeutic targets in HNSC. Targeting these transporters with small molecule inhibitors could disrupt essential supply routes for cancer cells, enhancing treatment efficacy and improving patient outcomes. This study paves the way for developing SLC-based target therapies in precision oncology, with the goal of improving survival rates for patients with HNSC.
头颈部鳞状细胞癌(HNSC)是头颈部最常见的癌症,起源于口腔、咽和喉的黏膜上皮。溶质载体(SLC)转运蛋白超家族由65个家族的400多种蛋白质组成,在细胞功能中起关键作用,是精准肿瘤学中很有前景的靶点。本研究旨在分析SLC转运蛋白在HNSC中的表达及其作为生物标志物和治疗靶点的潜力。
我们利用来自癌症基因组图谱(TCGA)和人类蛋白质图谱(HPA)的mRNA和蛋白质表达数据来检测HNSC中SLC转运蛋白的表达。进行基因集富集分析(GSEA)以评估SLC转运蛋白在各种致癌途径中的参与情况。
与正常组织相比,在肿瘤组织中观察到SLC转运蛋白显著上调,其中SLC16A3、SLC53A1、SLC25A32和SLC2A3有明显增加。这种上调与较差的总生存期(OS)和疾病特异性生存期(DSS)相关。GSEA显示,这些转运蛋白显著参与关键的致癌途径,包括上皮-间质转化(EMT)、血管生成和缺氧,这些对癌症进展和转移至关重要。
该研究确定SLC转运蛋白是HNSC中潜在的生物标志物和治疗靶点。用小分子抑制剂靶向这些转运蛋白可能会破坏癌细胞的重要供应途径,提高治疗效果并改善患者预后。本研究为在精准肿瘤学中开发基于SLC的靶向治疗铺平了道路,目标是提高HNSC患者的生存率。