Center of Hepato-Pancreato-Biliary Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China; Department of Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China; Institute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Department of Oncology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
J Hepatol. 2024 Aug;81(2):265-277. doi: 10.1016/j.jhep.2024.03.016. Epub 2024 Mar 19.
BACKGROUND & AIMS: Intrahepatic cholangiocarcinoma (iCCA) is the second most common primary liver cancer and is highly lethal. Clonorchis sinensis (C. sinensis) infection is an important risk factor for iCCA. Here we investigated the clinical impact and underlying molecular characteristics of C. sinensis infection-related iCCA.
We performed single-cell RNA sequencing, whole-exome sequencing, RNA sequencing, metabolomics and spatial transcriptomics in 251 patients with iCCA from three medical centers. Alterations in metabolism and the immune microenvironment of C. sinensis-related iCCAs were validated through an in vitro co-culture system and in a mouse model of iCCA.
We revealed that C. sinensis infection was significantly associated with iCCA patients' overall survival and response to immunotherapy. Fatty acid biosynthesis and the expression of fatty acid synthase (FASN), a key enzyme catalyzing long-chain fatty acid synthesis, were significantly enriched in C. sinensis-related iCCAs. iCCA cell lines treated with excretory/secretory products of C. sinensis displayed elevated FASN and free fatty acids. The metabolic alteration of tumor cells was closely correlated with the enrichment of tumor-associated macrophage (TAM)-like macrophages and the impaired function of T cells, which led to formation of an immunosuppressive microenvironment and tumor progression. Spatial transcriptomics analysis revealed that malignant cells were in closer juxtaposition with TAM-like macrophages in C. sinensis-related iCCAs than non-C. sinensis-related iCCAs. Importantly, treatment with a FASN inhibitor significantly reversed the immunosuppressive microenvironment and enhanced anti-PD-1 efficacy in iCCA mouse models treated with excretory/secretory products from C. sinensis.
We provide novel insights into metabolic alterations and the immune microenvironment in C. sinensis infection-related iCCAs. We also demonstrate that the combination of a FASN inhibitor with immunotherapy could be a promising strategy for the treatment of C. sinensis-related iCCAs.
Clonorchis sinensis (C. sinensis)-infected patients with intrahepatic cholangiocarcinoma (iCCA) have a worse prognosis and response to immunotherapy than non-C. sinensis-infected patients with iCCA. The underlying molecular characteristics of C. sinensis infection-related iCCAs remain unclear. Herein, we demonstrate that upregulation of FASN (fatty acid synthase) and free fatty acids in C. sinensis-related iCCAs leads to formation of an immunosuppressive microenvironment and tumor progression. Thus, administration of FASN inhibitors could significantly reverse the immunosuppressive microenvironment and further enhance the efficacy of anti-PD-1 against C. sinensis-related iCCAs.
肝内胆管癌(iCCA)是第二常见的原发性肝癌,具有高度致死性。华支睾吸虫(C. sinensis)感染是 iCCA 的一个重要危险因素。本研究旨在探讨华支睾吸虫感染相关 iCCA 的临床影响和潜在的分子特征。
我们对来自三个医疗中心的 251 例 iCCA 患者进行了单细胞 RNA 测序、全外显子组测序、RNA 测序、代谢组学和空间转录组学分析。通过体外共培养系统和 iCCA 小鼠模型验证了华支睾吸虫相关 iCCA 中代谢和免疫微环境的改变。
我们发现,华支睾吸虫感染与 iCCA 患者的总生存期和免疫治疗反应显著相关。脂肪酸生物合成和关键酶长链脂肪酸合成酶(FASN)的表达在华支睾吸虫相关 iCCA 中明显富集。用华支睾吸虫的分泌/排泄产物处理的 iCCA 细胞系显示 FASN 和游离脂肪酸水平升高。肿瘤细胞的代谢改变与肿瘤相关巨噬细胞(TAM)样巨噬细胞的富集以及 T 细胞功能受损密切相关,导致免疫抑制微环境的形成和肿瘤进展。空间转录组学分析显示,在华支睾吸虫相关 iCCA 中,恶性细胞与 TAM 样巨噬细胞的毗邻程度高于非华支睾吸虫相关 iCCA。重要的是,用 FASN 抑制剂治疗可显著逆转免疫抑制微环境,并增强华支睾吸虫分泌/排泄产物处理的 iCCA 小鼠模型中抗 PD-1 的疗效。
本研究提供了华支睾吸虫感染相关 iCCA 代谢改变和免疫微环境的新见解。还证明了 FASN 抑制剂与免疫疗法联合应用可能是治疗华支睾吸虫相关 iCCA 的一种有前途的策略。
与非华支睾吸虫感染的 iCCA 患者相比,感染华支睾吸虫的 iCCA 患者预后更差,对免疫治疗的反应更差。华支睾吸虫感染相关 iCCA 的潜在分子特征尚不清楚。本研究表明,华支睾吸虫相关 iCCA 中 FASN(脂肪酸合酶)和游离脂肪酸的上调导致免疫抑制微环境的形成和肿瘤进展。因此,FASN 抑制剂的给药可显著逆转免疫抑制微环境,并进一步增强抗 PD-1 对华支睾吸虫相关 iCCA 的疗效。