RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Targeting SNRPE to Induce Pyroptosis Enhances Antitumor Immunity in Breast Cancer.
Targeting SNRPE to Induce Pyroptosis Enhances Antitumor Immunity in Breast Cancer.
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尽管 SNRPE 是引导真核细胞 pre-mRNA 剪接的核心剪接体组分,但其对乳腺癌预后和免疫微环境的影响仍不清楚。细胞焦亡是一种炎症性细胞死亡,具有抑瘤功能并引发抗肿瘤免疫。理解控制细胞焦亡的通路将有助于开发特异性抗肿瘤策略,而 SNRPE 与细胞焦亡之间的关系尚未被研究。
为确定 SNRPE 对肿瘤预后的影响,对乳腺癌患者的临床样本进行了生存分析和免疫浸润评估。通过异种移植小鼠模型和细胞生物学实验,研究了靶向 SNRPE 的抗肿瘤作用及其进一步机制。
在此,我们发现 SNRPE 表达上调与不良肿瘤预后和低水平免疫浸润相关。我们的数据表明,靶向 SNRPE 通过在体内触发肿瘤细胞焦亡,激活了乳腺癌中自然杀伤(NK)细胞介导的抗肿瘤免疫。靶向 SNRPE 以 ROS 依赖性方式调节肿瘤细胞的焦亡。
本研究为剪接体靶向肿瘤与宿主免疫之间的相互作用提供了新见解,突出表明靶向剪接体以触发细胞焦亡是一种增强乳腺癌抗肿瘤免疫的综合治疗策略。
Background: Although SNRPE is a core spliceosomal component that guides pre-mRNA splicing in eukaryotic cells, its impact on mammary carcinoma prognosis and the immune microenvironment remains unclear. Pyroptosis, an inflammatory cell death, exerts tumor-suppressive functions and elicits antitumor immunity. Understanding the pathways that control pyroptosis will aid in developing specific antitumor strategies, while the relationship between SNRPE and pyroptosis has not been studied.
Methods: To determine the impact of SNRPE on tumor prognosis, survival analysis and immune infiltration assessment were performed on clinical samples from patients with breast cancer. The antitumor effects and further mechanisms of SNRPE targeting were investigated via the xenograft murine model and cell biology experiments. Results: Here, we found that upregulation of SNRPE expression was associated with unfavorable tumor prognosis and low levels of immune infiltration.
Our data identified SNRPE targeting activated natural killer (NK) cell-mediated antitumor immunity in breast cancer by triggering pyroptosis of tumor cells in vivo . SNRPE targeting modulated pyroptosis of tumor cells in a ROS-dependent manner. Conclusion: This study contributes to new insights into the interaction between spliceosome-targeted tumors and host immunity, highlighting the targeting of spliceosome to trigger pyroptosis as a comprehensive therapeutic strategy for enhanced antitumor immunity in breast cancer.
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