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胆管癌相关炎症分子机制的研究进展 被引量:2

Advances in the molecular mechanisms of inflammation associated with cholangiocarcinoma
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摘要 胆管系统的炎性疾病可能是胆管癌的危险因素。迄今为止,与慢性炎症相关的疾病,诸如肝内胆管结石、原发性硬化性胆管炎、Caroli病和吸虫感染等胆管癌(CCA)的前驱疾病研究较多,并且与CCA发生发展密切相关,也因此慢性炎症被认为是胆道良性疾病恶变的关键。因而,研究胆管炎症疾病的分子机制,有助于探索炎性因素导致胆管上皮细胞恶变向CCA的原因,为治疗CCA提供新的方向。本文结合近年来炎性因素导致胆道良性疾病向CCA恶变的研究进展,基于炎症相关分子机制在CCA发生发展中发挥的作用作一综述。 Inflammatory diseases of the biliary system may be a risk factor for cholangiocarcinoma(CCA).Thus far,research on precursor diseases related to chronic inflammation,such as intrahepatic bile duct stones,primary sclerosing cholangitis,Caroli’s disease,and parasitic infections,has been more prevalent and closely associated with the occurrence and development of CCA.Therefore,chronic inflammation is considered a key factor in the malignant transformation of benign biliary diseases.Studying the molecular mechanisms of biliary inflammatory diseases can help explore the reasons why inflammatory factors lead to the malignant transformation of biliary epithelial cells into CCA,and provide new directions for the treatment of CCA.This article provides a review of recent research on the malignant transformation of benign biliary diseases into CCA caused by inflammatory factors,based on the role played by inflammation-related molecular mechanisms in the occurrence and development of CCA.
作者 张硕 毛谅 陈骏 朱琳熙 陈超波 仇毓东 Zhang Shuo;Mao Liang;Chen jun;Zhu Linxi;Chen Chaobo;Qiu Yudong(Department of Hepatopancreatobiliary Surgery,Nanjing Drum Tower Hospital,the Affiliated Hospital of Nanjing University Medical School,Nanjing 210008,China;Department of Pathology,Nanjing Drum Tower Hospital,the Affiliated Hospital of Nanjing University Medical School,Nanjing 210008,China;Department of General Surgery,Wuxi Branch of Zhongda Hospital,Southeast University,Wuxi 214105,China)
出处 《中华实验外科杂志》 CAS 北大核心 2023年第10期2145-2150,共6页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金(31971518) 江苏省卫生与健康委员会重点项目(ZD2021017) 无锡市卫生与健康委员会面上项目(M202160)。
关键词 胆管癌 胆管良性疾病 炎症信号 分子机制 靶向治疗 Cholangiocarcinoma Benign diseases of the bile duct Inflammatory signals Molecular mechanisms Targeted therapy
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