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针对癌相关成纤维细胞诱导的白细胞介素-6治疗胃癌腹膜转移的新策略。

Novel treatment strategy targeting interleukin-6 induced by cancer associated fibroblasts for peritoneal metastasis of gastric cancer.

作者信息

Mitsui Ema, Kikuchi Satoru, Okura Tomohiro, Tazawa Hiroshi, Une Yuta, Nishiwaki Noriyuki, Kuroda Shinji, Noma Kazuhiro, Kagawa Shunsuke, Ohara Toshiaki, Ohtsuka Junko, Ohki Rieko, Fujiwara Toshiyoshi

机构信息

Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, 700-8558, Japan.

Center for Innovative Clinical Medicine, Okayama University Hospital, Okayama, 700-8558, Japan.

出版信息

Sci Rep. 2025 Jan 25;15(1):3267. doi: 10.1038/s41598-025-88033-0.


DOI:10.1038/s41598-025-88033-0
PMID:39863722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11762302/
Abstract

Cancer-associated fibroblasts (CAFs) are a crucial component in the tumor microenvironment (TME) of peritoneal metastasis (PM), where they contribute to tumor progression and metastasis via secretion of interleukin-6 (IL-6). Here, we investigated the role of IL-6 in PM of gastric cancer (GC) and assessed whether anti-IL-6 receptor antibody (anti-IL-6R Ab) could inhibit PM of GC. We conducted immunohistochemical analysis of IL-6 and α-smooth muscle (α-SMA) expressions in clinical samples of GC and PM, and investigated the interactions between CAFs and GC cells in vitro. Anti-tumor effects of anti-IL-6R Ab on PM of GC were investigated in an orthotopic murine PM model. IL-6 expression was significantly correlated with α-SMA expression in clinical samples of GC, and higher IL-6 expression in the primary tumor was associated with poor prognosis of GC. Higher IL-6 and α-SMA expressions were also observed in PM of GC. In vitro, differentiation of fibroblasts into CAFs and chemoresistance were observed in GC cells cocultured with fibroblasts. Anti-IL-6R Ab inhibited the progression of PM in GC cells cocultured with fibroblasts in the orthotopic mouse model but could not inhibit the progression of PM consisting of GC cells alone. IL-6 expression in the TME was associated with poor prognosis of GC, and CAFs were associated with establishment and progression of PM via IL-6. Anti-IL-6R Ab could inhibit PM of GC by the blockade of IL-6 secreted by CAFs, which suggests its therapeutic potential for PM of GC.

摘要

癌症相关成纤维细胞(CAFs)是腹膜转移(PM)肿瘤微环境(TME)的关键组成部分,它们通过分泌白细胞介素-6(IL-6)促进肿瘤进展和转移。在此,我们研究了IL-6在胃癌(GC)腹膜转移中的作用,并评估抗IL-6受体抗体(抗IL-6R Ab)是否能抑制GC的腹膜转移。我们对GC和PM临床样本中的IL-6和α-平滑肌(α-SMA)表达进行了免疫组化分析,并在体外研究了CAFs与GC细胞之间的相互作用。在原位小鼠腹膜转移模型中研究了抗IL-6R Ab对GC腹膜转移的抗肿瘤作用。在GC临床样本中,IL-6表达与α-SMA表达显著相关,原发肿瘤中较高的IL-6表达与GC的不良预后相关。在GC的PM中也观察到较高的IL-6和α-SMA表达。在体外,与成纤维细胞共培养的GC细胞中观察到成纤维细胞向CAFs的分化和化疗耐药性。抗IL-6R Ab在原位小鼠模型中抑制了与成纤维细胞共培养的GC细胞中腹膜转移的进展,但不能抑制仅由GC细胞组成的腹膜转移的进展。TME中的IL-6表达与GC的不良预后相关,CAFs通过IL-6与腹膜转移的建立和进展相关。抗IL-6R Ab可通过阻断CAFs分泌的IL-6来抑制GC的腹膜转移,这表明其对GC腹膜转移具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/5a78cf685e84/41598_2025_88033_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/0ffc593c4fa4/41598_2025_88033_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/7b4969a6bced/41598_2025_88033_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/27b1e6376e69/41598_2025_88033_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/5a78cf685e84/41598_2025_88033_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/0ffc593c4fa4/41598_2025_88033_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/7b4969a6bced/41598_2025_88033_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/27b1e6376e69/41598_2025_88033_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bba2/11762302/5a78cf685e84/41598_2025_88033_Fig4_HTML.jpg

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Novel treatment strategy targeting interleukin-6 induced by cancer associated fibroblasts for peritoneal metastasis of gastric cancer.

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本文引用的文献

[1]
Functional remodeling of intraperitoneal macrophages by oncolytic adenovirus restores anti-tumor immunity for peritoneal metastasis of gastric cancer.

Mol Ther Oncol. 2024-4-24

[2]
Therapeutic strategies for COVID-19: progress and lessons learned.

Nat Rev Drug Discov. 2023-6

[3]
How I treat refractory CRS and ICANS after CAR T-cell therapy.

Blood. 2023-5-18

[4]
Overcoming cancer-associated fibroblast-induced immunosuppression by anti-interleukin-6 receptor antibody.

Cancer Immunol Immunother. 2023-7

[5]
Japanese Gastric Cancer Treatment Guidelines 2021 (6th edition).

Gastric Cancer. 2023-1

[6]
Altered intraperitoneal immune microenvironment in patients with peritoneal metastases from gastric cancer.

Front Immunol. 2022

[7]
Modulation of expression in cancer-associated fibroblasts prevents peritoneal metastasis of gastric cancer.

Mol Ther Oncolytics. 2022-4-25

[8]
First-line nivolumab plus chemotherapy versus chemotherapy alone for advanced gastric, gastro-oesophageal junction, and oesophageal adenocarcinoma (CheckMate 649): a randomised, open-label, phase 3 trial.

Lancet. 2021-7-3

[9]
Inflammation-driven senescence-associated secretory phenotype in cancer-associated fibroblasts enhances peritoneal dissemination.

Cell Rep. 2021-2-23

[10]
Metastatic pattern in esophageal and gastric cancer: Influenced by site and histology.

World J Gastroenterol. 2020-10-21

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