End Binding Proteins: Drivers of Cancer Progression.

Dhakshmi Sasankan, Renu Mohan
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Abstract

Cancer, a complex and heterogeneous disease, continues to be a major global health concern. Despite advancements in diagnostics and therapeutics, the aggressive nature of certain cancers remain a significant challenge, necessitating a deeper understanding of the underlying molecular mechanisms driving their severity and progression. Cancer severity and progression depend on cellular properties such as cell migration, cell division, cell shape changes, and intracellular transport, all of which are driven by dynamic cellular microtubules. Dynamic properties of microtubules, in turn, are regulated by an array of proteins that influence their stability and growth. Among these regulators, End Binding (EB) proteins stand out as critical orchestrators of microtubule dynamics at their growing plus ends. Beyond their fundamental role in normal cellular functions, recent research has uncovered compelling evidence linking EB proteins to the pathogenesis of various diseases, including cancer progression. As the field of cancer research advances, the clinical implication of EB proteins role in cancer severity and aggressiveness become increasingly evident. This review aims to comprehensively explore the role of microtubule-associated EB proteins in influencing the severity and aggressiveness of cancer. We also discuss the potential significance of EB as a clinical biomarker for cancer diagnosis and prognosis and as a target for therapeutic intervention.

末端结合蛋白:癌症进展的驱动因素。
癌症是一种复杂的异质性疾病,仍然是一个主要的全球健康问题。尽管在诊断和治疗方面取得了进步,但某些癌症的侵袭性仍然是一个重大挑战,需要更深入地了解驱动其严重程度和进展的潜在分子机制。癌症的严重程度和进展取决于细胞特性,如细胞迁移、细胞分裂、细胞形状变化和细胞内运输,所有这些都是由动态细胞微管驱动的。微管的动态特性反过来又受到一系列影响其稳定性和生长的蛋白质的调节。在这些调节因子中,末端结合(EB)蛋白在其生长的正端作为微管动力学的关键协调者而脱颖而出。除了它们在正常细胞功能中的基本作用外,最近的研究还发现了将EB蛋白与包括癌症进展在内的各种疾病的发病机制联系起来的令人信服的证据。随着癌症研究领域的进步,EB蛋白在癌症严重程度和侵袭性中的临床意义越来越明显。本文旨在全面探讨微管相关EB蛋白在影响癌症严重程度和侵袭性中的作用。我们还讨论了EB作为癌症诊断和预后的临床生物标志物以及作为治疗干预目标的潜在意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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