血管生成及其生物标志物在开发肿瘤靶向治疗中的作用

IF 3.8 3区 医学 Q2 CELL & TISSUE ENGINEERING Stem Cells International Pub Date : 2024-01-04 DOI:10.1155/2024/9077926
Anchal Pathak, Ajay Kumar Pal, Subhadeep Roy, Mukesh Nandave, Keerti Jain
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引用次数: 0

摘要

血管生成在人体中扮演着重要角色,从伤口愈合到肿瘤进展都是如此。"血管生成转换 "指的是一个有时间限制的事件,在这个事件中,促血管生成因子和抗血管生成因子之间的不平衡导致从血管前增生过渡到血管化肿瘤的生长,最终导致恶性肿瘤的进展。在过去十年中,人们对参与肿瘤发生的分子角色,即血管生成生物标志物和潜在的分子通路进行了深入研究。通过靶向这些生物标志物和分子通路来破坏血管生成的启动和阻止其进展,已被认为是治疗肿瘤血管生成的一种潜在方法。本综述讨论了目前已知的生物标记物和可用的抗血管生成疗法,即单克隆抗体、适配体、小分子抑制剂、miRNAs、siRNAs、血管生长抑素、内生长抑素和褪黑激素类似物,这些药物或已获得美国食品药品管理局批准,或目前正在进行临床和临床前研究。
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Role of Angiogenesis and Its Biomarkers in Development of Targeted Tumor Therapies
Angiogenesis plays a significant role in the human body, from wound healing to tumor progression. “Angiogenic switch” indicates a time-restricted event where the imbalance between pro- and antiangiogenic factors results in the transition from prevascular hyperplasia to outgrowing vascularized tumor, which eventually leads to the malignant cancer progression. In the last decade, molecular players, i.e., angiogenic biomarkers and underlying molecular pathways involved in tumorigenesis, have been intensely investigated. Disrupting the initiation and halting the progression of angiogenesis by targeting these biomarkers and molecular pathways has been considered as a potential treatment approach for tumor angiogenesis. This review discusses the currently known biomarkers and available antiangiogenic therapies in cancer, i.e., monoclonal antibodies, aptamers, small molecular inhibitors, miRNAs, siRNAs, angiostatin, endostatin, and melatonin analogues, either approved by the U.S. Food and Drug Administration or currently under clinical and preclinical investigations.
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来源期刊
Stem Cells International
Stem Cells International CELL & TISSUE ENGINEERING-
CiteScore
8.10
自引率
2.30%
发文量
188
审稿时长
18 weeks
期刊介绍: Stem Cells International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of stem cell biology and applications. The journal will consider basic, translational, and clinical research, including animal models and clinical trials. Topics covered include, but are not limited to: embryonic stem cells; induced pluripotent stem cells; tissue-specific stem cells; stem cell differentiation; genetics and epigenetics; cancer stem cells; stem cell technologies; ethical, legal, and social issues.
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