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肝内与肝外胆管癌对 NK 细胞裂解的敏感性差异及通过共有与特异通路对 NK 细胞功能的调控

英文原题:Intra- and Extrahepatic Cholangiocarcinomas Display Differing Sensitivities to NK Cell Lysis and Modulate NK Cell Function through Shared and Distinct Pathways.

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Intra- and Extrahepatic Cholangiocarcinomas Display Differing Sensitivities to NK Cell Lysis and Modulate NK Cell Function through Shared and Distinct Pathways.

PubMed 2025/02/06(内容时间) Mol Cancer Res Q1 · IF 5.8(JCR 2025)

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中文摘要

胆管癌(CCA)是一种起源于胆管的罕见癌症,根据肿瘤位置大致分为肝内胆管癌(iCCA)或肝外胆管癌(eCCA)。免疫治疗已革新癌症治疗,但由于相较其他常见癌症,CCA 肿瘤微环境(TME)研究不足,免疫治疗在 CCA 中的应用有限。我们利用既往发表的转录组数据重新分析发现,与其他癌症相比,CCA 中强效细胞毒性免疫细胞 NK 细胞的相对水平处于最高之列。然而,尽管 iCCA 和 eCCA 的 NK 细胞浸润相对水平相近,只有 eCCA 患者中 NK 细胞浸润与生存相关。进一步研究显示,虽然 iCCA 和 eCCA 均显著改变 NK 活性,但 eCCA 对 NK 功能的影响显著较弱。iCCA 对长期 NK 共培养具有耐受性,而 eCCA 明显更敏感。此外,尽管 iCCA 和 eCCA 均使关键 NK 激活受体失调,eCCA 共培养并未影响 NKp30 或 NKp44 表达。对 NK 高浸润 CCA 样本的肿瘤转录组分析还显示,TME 中多种免疫和非免疫细胞类型发生调节。意义:本研究首次探讨 iCCA 和 eCCA 通过共同及不同机制影响 NK 细胞功能,并说明 NK 细胞浸润升高如何以亚型依赖方式塑造 CCA 肿瘤微环境。

展开英文摘要原文

Cholangiocarcinoma (CCA) is a rare cancer that arises from the bile duct and is broadly classified by the location of the tumor as either intrahepatic cholangiocarcinoma (iCCA) or extrahepatic cholangiocarcinoma (eCCA).

Immunotherapy has revolutionized cancer treatment, yet its utility in CCA has been limited as the tumor microenvironment (TME) in CCA is poorly understood compared with other common cancers. Utilizing previously published transcriptome data, our reanalysis has revealed that CCA has one of the highest relative levels of NK cells, a potent cytotoxic immune cell, compared with other cancers.

However, despite iCCA and eCCA having comparable relative levels of NK infiltration, NK cell infiltration only correlated with survival in patients with eCCA.

Our subsequent investigation revealed that although iCCA and eCCA profoundly altered NK activity, eCCA had a significantly reduced impact on NK functionality. Whereas iCCA was resistant to long-term NK coculture, eCCA was markedly more sensitive.

Moreover, although both iCCA and eCCA dysregulated key NK-activating receptors, eCCA coculture did not impact NKp30 nor NKp44 expression.

Furthermore, tumor transcriptome analysis of NKHigh CCA samples revealed a modulation of multiple immune and nonimmune cell types within the TME. Implications: These studies are the first to investigate how iCCA and eCCA impact NK cell functionality through shared and distinct mechanisms and how elevated NK cell infiltration could shape the CCA TME in a subtype-dependent manner.

论文信息

作者
Nguyen N、Henrich IC
单位
Department of Experimental Therapeutics, Baruch S. Blumberg Institute, Philadelphia, Pennsylvania.United States
文献类型
美国公共卫生署资助研究
期刊
Molecular cancer research : MCR2025 Feb 6
原文标识
PubMed 39436670 · DOI 10.1158/1541-7786.MCR-24-0299