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:Podocalyxin protects high grade serous ovarian cancer spheroids from NK cell infiltration and spheroid destruction.
Podocalyxin protects high grade serous ovarian cancer spheroids from NK cell infiltration and spheroid destruction.
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这些数据表明 PODXL 可能在 HGSC 中协助免疫逃逸方面发挥重要作用,至少部分是通过赋予对 NK 细胞浸润及相关细胞毒性的抵抗性。
高级别浆液性癌(HGSC)是卵巢癌中最常见且最致命的亚型,然而其预后在过去30年中一直未得到改善。已知HGSC会演化出免疫逃逸策略以促进生存,但这些机制尚未被充分理解。Podocalyxin(PODXL)是一种与CD34相关的唾液黏蛋白,常在预后不良的HGSC患者中表达。我们最近报道,PODXL促进致密且耐化疗的HGSC球体形成,从而增强其生存能力。
在本研究中,我们探讨了PODXL是否也可能影响HGSC球体对NK细胞浸润和细胞毒性的易感性。我们将HGSC球体与从外周血单核细胞(PBMCs)中分离的原代人NK细胞共培养,并检测了共培养24、48和72小时后对这些球体的影响。我们首先使用了Kuramochi细胞的HGSC球体细胞系模型,该细胞在已知HGSC细胞系中PODXL表达水平最高。为了研究PODXL水平的影响,我们比较了对照组和我们之前构建的PODXL敲除(PODXL-KO)细胞的球体。随后,我们在来源于HGSC患者腹水、表达高水平和低水平PODXL的原代癌症球体中验证了这些数据。
在细胞系和原代HGSC球体模型中,表达较低水平PODXL的球体共培养导致更多的NK细胞浸润和细胞毒性,而表达较高水平PODXL的球体则抵抗破坏并显示出更多的增殖。
High grade serous carcinoma (HGSC) is the most common and lethal subtype of ovarian cancer, yet its prognosis has remained unchanged in the past 3 decades. HGSC is known to have evolved immune evasion strategies to promote survival, but these mechanisms are not well understood. Podocalyxin (PODXL), a CD34-related sialomucin, is often expressed in HGSC patients with poor prognosis. We have recently reported that PODXL promotes the formation of compact and chemoresistant HGSC spheroids to boost their survival.
In this current study, we investigated whether PODXL may also influence HGSC spheroid susceptibility to NK cell infiltration and cytotoxicity. We co-cultured HGSC spheroids with primary human NK cells isolated from peripheral blood mononuclear cells (PBMCs) and examined the impact on these spheroids following 24, 48 and 72 h of co-culture. We first used a cell line model of HGSC spheroids employing Kuramochi cells, which express the highest level of PODXL among known HGSC cell lines. To study the impact of PODXL levels, we compared spheroids of control and PODXL knockout (PODXL-KO) cells that we have previously engineered. We then validated the data in primary cancer spheroids derived from ascites of HGSC patients that express high and low levels of PODXL.
In both the cell line and primary HGSC spheroid models, co-culture of spheroids expressing lower levels of PODXL resulted in more NK cell infiltration and cytotoxicity, while spheroids expressing higher levels of PODXL were resistant to destruction and showed more proliferation.
Collectively, these data suggest that PODXL may play an important role in aiding immune evasion in HGSC, at least partly by conferring resistance to NK cell infiltration and the related cytotoxicity.
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