Chatterjee Reshmi, Mitra Abhisek
E.S.I. Hospital, Belur, West Bengal, India.
University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Int Immunopharmacol. 2015 Feb;24(2):335-345. doi: 10.1016/j.intimp.2014.12.024. Epub 2015 Jan 3.
Chronic liver diseases (CLDs) such as hepatitis, alcoholic liver disease, nonalcoholic fatty liver, and their downstream effect cancer affect more than a billion of people around the world both symptomatically and asymptomatically. The major limitation for early detection and suitable medical management of CLDs and liver cancer is either the absent of symptoms or their similar manifestations as other diseases. This detection impediment has led to a steady increase in the number of people suffering from CLDs with an ultimate outcome of liver failure and undergoing transplantation. A better understanding of CLD pathogenesis has helped us to develop novel therapies for patients who are at greatest risk for CLD progression to the most serious disease cancer. With the discovery of aberrant molecular pathways in CLDs, it is now possible to delineate a road map for selecting targeted therapies for CLDs. Technological advances in imaging as well as the availability of several stable, sensitive, early, noninvasive biomarkers for distinguishing different stages of CLDs and cancer have greatly facilitated both drug target identification and real-time monitoring of response to therapy. Biomarkers are the most useful in clinical practice for liver diseases like hepatocellular carcinoma (HCC), which is associated with secretion of various tumor-related proteins or nucleotides in peripheral circulation. The need for the identification of CLD biomarkers remains high. This article reviews the etiologies of CLDs, the results of recent clinical trials of treatments for CLDs, and development of noninvasive methodologies for detecting CLDs and monitoring their progression toward HCC.
慢性肝病(CLD),如肝炎、酒精性肝病、非酒精性脂肪性肝病及其下游效应癌症,无论有无症状,都影响着全球超过10亿人。CLD和肝癌早期检测及适当医疗管理的主要限制在于要么无症状,要么症状与其他疾病相似。这种检测障碍导致患CLD的人数稳步增加,最终导致肝功能衰竭并接受移植。对CLD发病机制的更好理解有助于我们为最有可能从CLD进展为最严重疾病癌症的患者开发新疗法。随着CLD中异常分子途径的发现,现在有可能勾勒出一条为CLD选择靶向治疗的路线图。成像技术的进步以及几种用于区分CLD和癌症不同阶段的稳定、敏感、早期、非侵入性生物标志物的可用性,极大地促进了药物靶点的识别和治疗反应的实时监测。生物标志物在肝细胞癌(HCC)等肝病的临床实践中最有用,HCC与外周循环中各种肿瘤相关蛋白质或核苷酸的分泌有关。对CLD生物标志物的识别需求仍然很高。本文综述了CLD的病因、CLD治疗的近期临床试验结果以及检测CLD并监测其向HCC进展的非侵入性方法的发展。