原发性肝癌中筋膜蛋白-1的靶向治疗前景

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Lydia Dif , Grégoire Manaud , Violaine Moreau
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引用次数: 0

摘要

原发性肝癌是全球癌症相关死亡的第三大原因。尽管有了化疗、免疫疗法和抗血管生成药物,但生存率并没有提高。更糟糕的是,大多数患者对最有效的治疗没有反应。患者分层是必要的,以增加有效治疗的可能性。我们确实需要更有针对性的治疗方法。在这里,我们概述了一种f -肌动蛋白捆绑蛋白fastin -1在细胞迁移和侵袭中的作用。我们关注其在肝脏肿瘤发生中的影响和临床意义。我们建议fasin -1作为原发性肝癌(包括肝细胞癌、胆管癌和肝母细胞瘤)预后不良的标志物。在所有这些癌症中发现了fasin -1的过度表达,并且通常与未分化的肿瘤和更糟糕的结果相关。然后,我们回顾了目前针对原发性肝癌靶向fasin -1的方法。最后,我们提供了可能促进癌症研究的观点,并为肝癌及其他癌症的筋膜蛋白靶向治疗开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fascin-1 in primary liver cancers, perspectives for targeted therapy
Primary liver cancers are the third leading cause of cancer-related deaths worldwide. Despite the availability of chemotherapeutics, immunotherapies and anti-angiogenic drugs, survival rates have not improved. Worse, most patients do not respond to the most effective therapies. Patient stratification is necessary to increase the likelihood of effective treatment. More targeted therapies are definitely needed. Here, we provide an overview of the role of Fascin-1, an F-actin-bundling protein, in cell migration and invasion. We focus on its impact and clinical relevance in liver tumorigenesis. We propose Fascin-1 as a marker of poor prognosis for primary liver cancers including hepatocellular carcinoma, cholangiocarcinoma and hepatoblastoma. Fascin-1 is found to be overexpressed in all these cancers and is usually associated with undifferentiated tumors and worse outcomes. We then review current approaches to targeting Fascin-1 in primary liver cancers. Finally, we offer perspectives that may foster cancer research and open new avenues for Fascin-targeted therapies in liver cancers and beyond.
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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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