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埃兹蛋白在骨肉瘤转移中的作用。

Role of ezrin in osteosarcoma metastasis.

机构信息

Molecular Oncology Section - Metastasis Biology Group, Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 37 Convent Dr., Rm 2144, Bethesda, MD, 20892, USA,

出版信息

Adv Exp Med Biol. 2014;804:181-201. doi: 10.1007/978-3-319-04843-7_10.

Abstract

The cause of death for the vast majority of cancer patients is the development of metastases at sites distant from that of the primary tumor. For most pediatric sarcoma patients such as those with osteosarcoma (OS), despite successful management of the primary tumor through multimodality approaches, the development of metastases, commonly to the lungs, is the cause of death. Significant improvements in long-term outcome for these patients have not been seen in more than 30 years. Furthermore, the long-term outcome for patients who present with metastatic disease is grave [1-5]. New treatment options are needed.Opportunities to improve outcomes for patients who present with metastases and those at-risk for progression and metastasis require an improved understanding of cancer progression and metastasis. With this goal in mind we and others have identified ezrin as a metastasis-associated protein that associated with OS and other cancers. Ezrin is the prototypical ERM (Ezrin/Radixin/Moesin) protein family member. ERMs function as linker proteins connecting the actin cytoskeleton and the plasma membrane. Since our initial identification of ezrin in pediatric sarcoma, an increasing understanding the role of ezrin in metastasis has emerged. Briefly, ezrin appears to allow metastatic cells to overcome a number of stresses experienced during the metastatic cascade, most notably the stress experienced as cells interact with the microenvironment of the secondary site. Cells must rapidly adapt to this environment in order to survive. Evidence now suggests a connection between ezrin expression and a variety of mechanisms linked to this important cellular adaptation including the ability of metastatic cells to initiate the translation of new proteins and to allow the efficient generation of ATP through a variety of sources. This understanding of the role of ezrin in the biology of metastasis is now sufficient to consider ezrin as an important therapeutic target in osteosarcoma patients. This chapter reviews our understanding of ezrin and the related ERM proteins in normal tissues and physiology, summarizes the expression of ezrin in human cancers and associations with clinical parameters of disease progression, reviews reports that detail a biological understanding of ezrin's role in metastatic progression, and concludes with a rationale that may be considered to target ezrin and ezrin biology in osteosarcoma.

摘要

绝大多数癌症患者的死亡原因是原发肿瘤远处转移的发展。对于大多数儿科肉瘤患者,如骨肉瘤(OS)患者,尽管通过多模式方法成功治疗了原发肿瘤,但转移的发展,通常是肺部转移,仍是导致死亡的原因。30 多年来,这些患者的长期预后并未得到显著改善。此外,患有转移性疾病的患者的长期预后是严峻的[1-5]。需要新的治疗选择。

为了改善出现转移和有进展和转移风险的患者的预后,需要更好地了解癌症的进展和转移。考虑到这一目标,我们和其他人已经确定 ezrin 是一种与骨肉瘤和其他癌症相关的转移相关蛋白。Ezrin 是典型的 ERM(Ezrin/Radixin/Moesin)蛋白家族成员。ERM 作为连接肌动蛋白细胞骨架和质膜的连接蛋白发挥作用。自我们最初在儿科肉瘤中鉴定出 ezrin 以来,人们对 ezrin 在转移中的作用的认识逐渐加深。简而言之,ezrin 似乎使转移性细胞能够克服转移级联过程中经历的许多应激,特别是当细胞与次级部位的微环境相互作用时所经历的应激。细胞必须迅速适应这种环境才能存活。现在的证据表明 ezrin 表达与多种与这种重要细胞适应相关的机制之间存在联系,包括转移性细胞启动新蛋白质翻译的能力以及通过多种来源允许有效生成 ATP 的能力。对 ezrin 在转移生物学中的作用的这种理解足以将其视为骨肉瘤患者的重要治疗靶点。本章回顾了我们对 ezrin 及其在正常组织和生理学中的相关 ERM 蛋白的理解,总结了 ezrin 在人类癌症中的表达及其与疾病进展临床参数的关联,回顾了详细描述 ezrin 在转移进展中的生物学作用的报告,并得出了一个合理的结论,即可能考虑针对 ezrin 及其在骨肉瘤中的生物学作用进行靶向治疗。

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