Second Department of Surgery, Wakayama Medical University, Wakayama, Japan.
Department of Human Pathology, Wakayama Medical University, Wakayama, Japan.
PLoS One. 2022 Mar 24;17(3):e0265908. doi: 10.1371/journal.pone.0265908. eCollection 2022.
The interaction of CD155 with its ligand, the T cell immunoreceptor with Ig and ITIM domains (TIGIT), is being studied owing to its potential to act as a target in the treatment of various solid tumors. However, the relationship between CD155 and TIGIT in colorectal cancer (CRC) prognosis is not known. We hypothesized that the TIGIT-CD155 pathway suppresses the attack of T cells on tumors, thereby affecting CRC prognosis.
We examined the expression of CD155 and TIGIT using immunohistochemical staining in 100 consecutive patients with CRC who underwent complete resection of ≤Stage III tumors at Wakayama Medical University Hospital between January and December 2013. We assessed the correlation between CD155 and TIGIT expressions and prognosis as well as the clinicopathological background of CD155 and TIGIT.
Patients with high CD155 and TIGIT expressions showed worse prognosis than those with other levels of expression (p = 0.026). In multivariate analysis that also included the existing prognostic markers, high CD155 and TIGIT expressions were identified as independent poor prognostic factors.
The interaction between CD155 and TIGIT possibly plays an important role in the immunological mechanism of CRC. Therefore, it may be possible to effectively predict the postoperative prognosis of CRC by evaluating the combined expression of CD155 and TIGIT. The study findings suggest that CD155 and TIGIT can predict clinical outcomes, thereby contributing to the personalized care of CRC.
由于 CD155 与其配体 T 细胞免疫受体含免疫球蛋白和 ITIM 结构域(TIGIT)相互作用,因此正在对其进行研究,因为它可能成为治疗各种实体瘤的靶点。然而,CD155 和 TIGIT 在结直肠癌(CRC)预后中的关系尚不清楚。我们假设 TIGIT-CD155 途径抑制 T 细胞对肿瘤的攻击,从而影响 CRC 的预后。
我们使用免疫组织化学染色法检测了 2013 年 1 月至 12 月在和歌山医科大学医院接受≤III 期肿瘤完全切除术的 100 例连续 CRC 患者的 CD155 和 TIGIT 表达。我们评估了 CD155 和 TIGIT 表达与预后之间的相关性,以及 CD155 和 TIGIT 的临床病理背景。
高 CD155 和 TIGIT 表达的患者比其他表达水平的患者预后更差(p = 0.026)。在包括现有预后标志物的多变量分析中,高 CD155 和 TIGIT 表达被确定为独立的不良预后因素。
CD155 和 TIGIT 之间的相互作用可能在 CRC 的免疫机制中发挥重要作用。因此,通过评估 CD155 和 TIGIT 的联合表达,可能可以有效地预测 CRC 的术后预后。研究结果表明,CD155 和 TIGIT 可以预测临床结局,从而有助于 CRC 的个体化治疗。