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Exploring Novel Molecular Targets for the Treatment of High-Grade Astrocytomas Using Peptide Therapeutics: An Overview

机译:探索新的分子靶标治疗高级别星形细胞瘤的肽疗法:概述。

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摘要

Diffuse astrocytomas are the most aggressive and lethal glial tumors of the central nervous system (CNS). Their high cellular heterogeneity and the presence of specific barriers, i.e., blood–brain barrier (BBB) and tumor barrier, make these cancers poorly responsive to all kinds of currently available therapies. Standard therapeutic approaches developed to prevent astrocytoma progression, such as chemotherapy and radiotherapy, do not improve the average survival of patients. However, the recent identification of key genetic alterations and molecular signatures specific for astrocytomas has allowed the advent of novel targeted therapies, potentially more efficient and characterized by fewer side effects. Among others, peptides have emerged as promising therapeutic agents, due to their numerous advantages when compared to standard chemotherapeutics. They can be employed as (i) pharmacologically active agents, which promote the reduction of tumor growth; or (ii) carriers, either to facilitate the translocation of drugs through brain, tumor, and cellular barriers, or to target tumor-specific receptors. Since several pathways are normally altered in malignant gliomas, better outcomes may result from combining multi-target strategies rather than targeting a single effector. In the last years, several preclinical studies with different types of peptides moved in this direction, providing promising results in murine models of disease and opening new perspectives for peptide applications in the treatment of high-grade brain tumors.
机译:弥漫性星形细胞瘤是中枢神经系统(CNS)最具侵袭性和致死性的神经胶质瘤。它们的高细胞异质性和特定屏障的存在,即血脑屏障(BBB)和肿瘤屏障,使这些癌症对目前所有可用疗法的反应较差。为防止星形细胞瘤进展而开发的标准治疗方法,例如化学疗法和放射疗法,并不能提高患者的平均存活率。然而,最近对星形细胞瘤特异的关键遗传改变和分子标记的鉴定使得新的靶向疗法出现了,它可能更有效并且具有较少的副作用。其中,由于与标准化学疗法相比具有众多优势,因此肽已成为有前途的治疗剂。它们可用作(i)促进肿瘤生长减少的药理活性剂; (ii)载体,以促进药物通过脑,肿瘤和细胞屏障的转运,或靶向肿瘤特异性受体。由于在恶性神经胶质瘤中通常会改变几种途径,因此结合多靶点策略而非靶向单一效应子可能会产生更好的结果。在过去的几年中,一些针对不同类型肽的临床前研究朝着这一方向发展,在鼠类疾病模型中提供了令人鼓舞的结果,并为治疗高级脑肿瘤的肽应用开辟了新的前景。

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