The aminophospholipid transporter, ATP8B3, as a potential biomarker and target for enhancing the therapeutic effect of PD-L1 blockade in colon adenocarcinoma

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-27 DOI:10.1016/j.ygeno.2024.110907
Weihao Zhang , Yongjie Xie , Ziyun Liu , Jie Zhang , Bo Ni , Wei Gao , Wenge Xing , Yaoyao Zhou , Tongguo Si
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Abstract

Background

Colon adenocarcinoma (COAD) is a prevalent malignant tumor globally, contributing significantly to cancer-related mortality. COAD guidelines label MSI (Microsatellite instability) and MSS (Microsatellite stability) subtypes as global classification criteria and treatment strategy selection criteria for COAD. Various combination therapies involving PD-L1 inhibitors and adjuvant therapy to enhance anti-tumor efficacy.

Methods

Datasets from single-cell RNA sequencing and bulk RNA sequencing in the TCGA and GEO databases were utilized to identify differentially expressed genes (DEGs). Furthermore, the correlation between ATP8B3 and PD-L1 was validated using siRNA, shRNA, and western blot analysis. Additionally, the association between ATP8B3 and immune checkpoint blockade (ICB) therapy was investigated through immune infiltration analysis and flow cytometry in both in vivo and in vitro assays.

Results

In the COAD patient group, ATP8B3 significantly contributed to the establishment of an immunosuppressive microenvironment. Inhibiting ATP8B3 led to a reduction in PD-L1 expression in colon cancer cell lines. Additionally, ATP8B3 expression levels could serve as a potential guide for PD-L1 treatment in MSI-H COAD patients, with higher ATP8B3 expression associated with increased sensitivity to PD-L1 therapy. However, due to the lack of immuno-killer cells in the microenvironment of MSS subtypes, elevated ATP8B3 expression couldn't increase the sensitivity of MSS COAD patients to PD-L1 inhibitors.

Conclusion

Our research results support that Inhibiting ATP8B3 could enhance TIL (tumor-infiltrating lymphocyte) infiltration by reducing PD-L1 expression in MSI-H COAD, thereby serving as an effective strategy to improve PD-L1 blocker efficacy. The treatment strategy of combining ATP8B3 inhibitors and immunotherapy for MSI/MSS COAD patients will be the best choice.

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氨基磷脂转运体 ATP8B3 作为一种潜在的生物标记物和靶点,可增强 PD-L1 阻断剂对结肠腺癌的治疗效果。
背景:结肠腺癌(COAD)是一种全球流行的恶性肿瘤,是导致癌症相关死亡率的重要因素。COAD指南将MSI(微卫星不稳定性)和MSS(微卫星稳定性)亚型作为COAD的全球分类标准和治疗策略选择标准。PD-L1抑制剂和辅助治疗等多种联合疗法可提高抗肿瘤疗效:方法:利用TCGA和GEO数据库中的单细胞RNA测序数据集和大容量RNA测序数据集来鉴定差异表达基因(DEGs)。此外,还利用 siRNA、shRNA 和 Western 印迹分析验证了 ATP8B3 与 PD-L1 之间的相关性。此外,还通过体内和体外试验中的免疫浸润分析和流式细胞术研究了ATP8B3与免疫检查点阻断(ICB)疗法之间的关联:结果:在COAD患者组中,ATP8B3对免疫抑制微环境的建立起了重要作用。抑制 ATP8B3 可减少结肠癌细胞系中 PD-L1 的表达。此外,ATP8B3表达水平可作为MSI-H COAD患者PD-L1治疗的潜在指导,ATP8B3表达越高,对PD-L1治疗的敏感性越高。然而,由于MSS亚型的微环境中缺乏免疫杀伤细胞,ATP8B3表达的升高并不能增加MSS COAD患者对PD-L1抑制剂的敏感性:我们的研究结果表明,抑制ATP8B3可以通过降低PD-L1在MSI-H COAD中的表达来增强TIL(肿瘤浸润淋巴细胞)的浸润,从而成为提高PD-L1阻滞剂疗效的有效策略。对于MSI/MSS COAD患者,ATP8B3抑制剂与免疫疗法相结合的治疗策略将是最佳选择。
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CiteScore
7.20
自引率
4.30%
发文量
567
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