Department of Chest Surgery, Fukushima Medical University, Fukushima, Japan.
Advanced Clinical Research Center, Fukushima Medical University, Fukushima, Japan.
Lung Cancer. 2021 Mar;153:134-142. doi: 10.1016/j.lungcan.2021.01.014. Epub 2021 Jan 14.
Delta-like 1 homolog (DLK1) is a non-canonical Notch ligand known to be expressed in several cancers but whose role in lung cancer is not yet fully understood. We sought to confirm DLK1 expression in small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC), and to examine DLK1's clinical significance. Furthermore, we examined the possible utility of DLK1 as a novel target in radioimmunotherapy (RIT).
We retrospectively assessed the correlation between clinical features and DLK1 expression by immunohistochemistry in resected specimens from 112 patients with SCLC and 101 patients with NSCLC. Moreover, we performed cell and animal experiments, and examined the possibility of RIT targeting DLK1 in SCLC using iodine-125 (I) -labeled anti-DLK1 antibody, knowing that I can be replaced with the alpha-particle-emitter astatine-211 (At).
In SCLC and NSCLC, 20.5 % (23/112) and 16.8 % (17/101) of patients (respectively) had DLK1-positive tumors. In NSCLC, DLK1 expression was associated with recurrence-free survival (P < 0.01) but not with overall survival. In SCLC, there was no association between DLK1 expression and survival. In addition, I-labeled anti-DLK1 antibody specifically targeted DLK1 on human SCLC tumor cell lines. Furthermore, I-labeled anti-DLK1 antibody was incorporated into tumor tissue in a mouse model.
A proportion of SCLC and NSCLC exhibits DLK1 expression. As a clinical feature, DLK1 expression could be a promising prognostic factor for recurrence in patients with resected NSCLC. In addition, DLK1 could serve as a new therapeutic target, including RIT, as suggested by our pilot study using a radiolabeled anti-DLK1 antibody in SCLC.
Delta-like 1 同源物(DLK1)是一种非经典的 Notch 配体,已知在几种癌症中表达,但在肺癌中的作用尚不完全清楚。我们试图确认 DLK1 在小细胞肺癌(SCLC)和非小细胞肺癌(NSCLC)中的表达,并研究 DLK1 的临床意义。此外,我们还研究了将 DLK1 作为放射性免疫治疗(RIT)的新靶点的可能性。
我们通过免疫组织化学方法,对 112 例 SCLC 和 101 例 NSCLC 患者的手术标本进行回顾性评估,分析临床特征与 DLK1 表达的相关性。此外,我们进行了细胞和动物实验,研究了用碘-125(I)标记的抗-DLK1 抗体靶向 SCLC 中的 DLK1 的可能性,因为我们知道 I 可以被发射α粒子的放射性核素锕-211(At)取代。
在 SCLC 和 NSCLC 中,分别有 20.5%(23/112)和 16.8%(17/101)的患者肿瘤存在 DLK1 阳性表达。在 NSCLC 中,DLK1 表达与无复发生存率相关(P<0.01),但与总生存率无关。在 SCLC 中,DLK1 表达与生存无相关性。此外,I 标记的抗-DLK1 抗体特异性靶向人 SCLC 肿瘤细胞系上的 DLK1。此外,I 标记的抗-DLK1 抗体在小鼠模型中被整合到肿瘤组织中。
一部分 SCLC 和 NSCLC 存在 DLK1 表达。作为一种临床特征,DLK1 表达可能是预测 NSCLC 患者切除后复发的一个很有前途的预后因素。此外,正如我们用放射性标记的抗-DLK1 抗体在 SCLC 中进行的初步研究所示,DLK1 可以作为一种新的治疗靶点,包括 RIT。