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肝细胞癌-胆管细胞癌源于肝祖细胞,并依赖衰老和 IL-6 转导信号。

Combined hepatocellular-cholangiocarcinoma derives from liver progenitor cells and depends on senescence and IL-6 trans-signaling.

机构信息

Goldyne Savad Institute of Gene and Cell Therapy, Hadassah Hebrew University Hospital, Jerusalem, Israel.

Department of Imaging and Pathology, Translational Cell and Tissue Research, KU Leuven and University Hospitals Leuven, Leuven, Belgium; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, the Netherlands.

出版信息

J Hepatol. 2022 Dec;77(6):1631-1641. doi: 10.1016/j.jhep.2022.07.029. Epub 2022 Aug 18.

Abstract

BACKGROUND & AIMS: Primary liver cancers include hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (CCA) and combined HCC-CCA tumors (cHCC-CCA). It has been suggested, but not unequivocally proven, that hepatic progenitor cells (HPCs) can contribute to hepatocarcinogenesis. We aimed to determine whether HPCs contribute to HCC, cHCC-CCA or both types of tumors.

METHODS

To trace progenitor cells during hepatocarcinogenesis, we generated Mdr2-KO mice that harbor a yellow fluorescent protein (YFP) reporter gene driven by the Foxl1 promoter which is expressed specifically in progenitor cells. These mice (Mdr2-KO) develop chronic inflammation and HCCs by the age of 14-16 months, followed by cHCC-CCA tumors at the age of 18 months.

RESULTS

In this Mdr2-KO mouse model, liver progenitor cells are the source of cHCC-CCA tumors, but not the source of HCC. Ablating the progenitors, caused reduction of cHCC-CCA tumors but did not affect HCCs. RNA-sequencing revealed enrichment of the IL-6 signaling pathway in cHCC-CCA tumors compared to HCC tumors. Single-cell RNA-sequencing (scRNA-seq) analysis revealed that IL-6 is expressed by immune and parenchymal cells during senescence, and that IL-6 is part of the senescence-associated secretory phenotype. Administration of an anti-IL-6 antibody to Mdr2-KO mice inhibited the development of cHCC-CCA tumors. Blocking IL-6 trans-signaling led to a decrease in the number and size of cHCC-CCA tumors, indicating their dependence on this pathway. Furthermore, the administration of a senolytic agent inhibited IL-6 and the development of cHCC-CCA tumors.

CONCLUSION

Our results demonstrate that cHCC-CCA, but not HCC tumors, originate from HPCs, and that IL-6, which derives in part from cells in senescence, plays an important role in this process via IL-6 trans-signaling. These findings could be applied to develop new therapeutic approaches for cHCC-CCA tumors.

LAY SUMMARY

Combined hepatocellular carcinoma-cholangiocarcinoma is the third most prevalent type of primary liver cancer (i.e. a cancer that originates in the liver). Herein, we show that this type of cancer originates in stem cells in the liver and that it depends on inflammatory signaling. Specifically, we identify a cytokine called IL-6 that appears to be important in the development of these tumors. Our results could be used for the development of novel treatments for these aggressive tumors.

摘要

背景与目的

原发性肝癌包括肝细胞癌(HCC)、肝内胆管癌(CCA)和 HCC-CCA 混合型肿瘤(cHCC-CCA)。虽然有研究表明肝祖细胞(HPCs)可能参与肝癌的发生,但这一结论尚未得到明确证实。本研究旨在确定 HPCs 是否参与 HCC、cHCC-CCA 或这两种类型的肿瘤形成。

方法

为了在肝癌发生过程中追踪祖细胞,我们构建了 Mdr2-KO 小鼠模型,该模型的 Foxl1 启动子驱动的黄色荧光蛋白(YFP)报告基因可特异性表达于祖细胞。这些 Mdr2-KO 小鼠在 14-16 月龄时会发展为慢性炎症和 HCC,在 18 月龄时则会发展为 cHCC-CCA 肿瘤。

结果

在 Mdr2-KO 小鼠模型中,肝祖细胞是 cHCC-CCA 肿瘤的来源,而不是 HCC 的来源。祖细胞缺失会导致 cHCC-CCA 肿瘤减少,但不会影响 HCC。RNA 测序显示,与 HCC 肿瘤相比,cHCC-CCA 肿瘤中 IL-6 信号通路富集。单细胞 RNA 测序(scRNA-seq)分析显示,IL-6 在衰老的免疫细胞和实质细胞中表达,并且是衰老相关分泌表型的一部分。给 Mdr2-KO 小鼠注射抗 IL-6 抗体可抑制 cHCC-CCA 肿瘤的发展。阻断 IL-6 转导信号会导致 cHCC-CCA 肿瘤的数量和大小减少,表明其对该途径的依赖性。此外,使用 senolytic 药物可抑制 IL-6 的表达并减少 cHCC-CCA 肿瘤的发生。

结论

本研究结果表明,cHCC-CCA 肿瘤而非 HCC 肿瘤起源于 HPCs,部分来源于衰老细胞的细胞因子 IL-6 通过 IL-6 转导信号在该过程中发挥重要作用。这些发现可用于开发治疗 cHCC-CCA 肿瘤的新方法。

以上译文仅供参考,具体内容可根据实际情况进行调整。

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