The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, China.
Department of Oral Maxillofacial-Head Neck Oncology, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, China.
Biomolecules. 2023 Jun 19;13(6):1014. doi: 10.3390/biom13061014.
Integrin β4 (ITGB4) is a member of the integrin family, which plays a crucial role in mediating cell adhesion to the extracellular matrix. Recent studies have demonstrated that ITGB4 is involved in tumorigenesis and metastasis during the development of cancer. However, the role of ITGB4 in oral squamous cell carcinoma (OSCC) remains unclear. A Multiplex immunohistochemistry (OPAL™, mIHC) assay was employed to stain ITGB4, ALDH1, PD-L1, cytokeratin (CK), CD8 and PD-1 in a human OSCC tissue microarray, containing 26 normal oral epithelium samples, 21 oral epithelium dysplasia samples and 76 OSCC samples. The expression pattern and clinicopathological characteristics of ITGB4 were analyzed and compared with those of PD-1, PD-L1, ALDH1 and CD8. The correlation between subgroups of tumor cells, including ITGB4PD-L1 and ITGB4ALDH1, and subgroups of T cells, including CD8 and CD8PD-1, was evaluated using two-tailed Pearson's statistics. A Kaplan-Meier curve was built, and a log-rank test was performed to analyze the survival rate of different subgroups. The mIHC staining results show that ITGB4 was mostly expressed in the tumor cells, with a significant increase in the OSCC specimens compared with normal oral epithelium and oral epithelium dysplasia. The paired analysis, conducted between the OSCC tumor tissue and normal paracancer mucosa, confirmed the results. The study further revealed that ITGB4PD-L1 cancer cells, but not ITGB4ALDH1 cancer cells, were significantly associated with the infiltration of CD8 T cells (positivity = 0.005, positive number = 0.03). Additionally, ITGB4PD-L1 tumor cells were positively correlated with CD8PD-1 T cells (positivity = 0.02, positive number = 0.03). Most intriguingly, the subgroup of ITGB4/PD-L1 with CD8/PD-1 displayed the best prognosis compared with the other considered subgroups. The results show that the expression of ITGB4 was increased in OSCC compared with normal oral mucosa. Furthermore, a specific subgroup with high levels of expression of ITGB4/PD-L1 and CD8/PD-1 was found to have a relatively better prognosis compared with the other subgroups. Ultimately, this study sheds light on the potential role of ITGB4 in OSCC and provides a basis for further investigation.
整合素 β4 (ITGB4) 是整合素家族的一员,在介导细胞与细胞外基质的黏附中起着至关重要的作用。最近的研究表明,ITGB4 参与了癌症发展过程中的肿瘤发生和转移。然而,ITGB4 在口腔鳞状细胞癌 (OSCC) 中的作用仍不清楚。采用多重免疫组化 (OPAL ™, mIHC) 检测试剂盒对包含 26 例正常口腔上皮样本、21 例口腔上皮异型增生样本和 76 例 OSCC 样本的人类 OSCC 组织微阵列中的 ITGB4、ALDH1、PD-L1、细胞角蛋白 (CK)、CD8 和 PD-1 进行染色。分析 ITGB4 的表达模式和临床病理特征,并与 PD-1、PD-L1、ALDH1 和 CD8 进行比较。采用双尾 Pearson 统计学评估 ITGB4PD-L1 和 ITGB4ALDH1 肿瘤细胞亚群与 CD8 和 CD8PD-1 T 细胞亚群之间的相关性。构建 Kaplan-Meier 曲线,并进行对数秩检验分析不同亚组的生存率。mIHC 染色结果显示,ITGB4 主要在肿瘤细胞中表达,与正常口腔上皮和口腔上皮异型增生相比,OSCC 标本中的表达显著增加。对 OSCC 肿瘤组织与正常癌旁黏膜之间进行配对分析,证实了这一结果。研究进一步表明,ITGB4PD-L1 肿瘤细胞而非 ITGB4ALDH1 肿瘤细胞与 CD8 T 细胞浸润显著相关(阳性率 = 0.005,阳性细胞数 = 0.03)。此外,ITGB4PD-L1 肿瘤细胞与 CD8PD-1 T 细胞呈正相关(阳性率 = 0.02,阳性细胞数 = 0.03)。最有趣的是,与其他考虑的亚组相比,ITGB4/PD-L1 与 CD8/PD-1 的亚组具有最佳的预后。结果表明,与正常口腔黏膜相比,OSCC 中 ITGB4 的表达增加。此外,发现具有高表达 ITGB4/PD-L1 和 CD8/PD-1 的特定亚组与其他亚组相比,预后相对较好。最终,本研究揭示了 ITGB4 在 OSCC 中的潜在作用,并为进一步研究提供了依据。