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了解 Notch 在骨肉瘤中的作用。

Understanding the role of Notch in osteosarcoma.

机构信息

The Children's Cancer Hospital at MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Adv Exp Med Biol. 2014;804:67-92. doi: 10.1007/978-3-319-04843-7_4.

Abstract

The Notch pathway has been described as an oncogene in osteosarcoma, but the myriad functions of all the members of this complex signaling pathway, both in malignant cells and nonmalignant components of tumors, make it more difficult to define Notch as simply an oncogene or a tumor suppressor. The cell-autonomous behaviors caused by Notch pathway manipulation may vary between cell lines but can include changes in proliferation, migration, invasiveness, oxidative stress resistance, and expression of markers associated with stemness or tumor-initiating cells. Beyond these roles, Notch signaling also plays a vital role in regulating tumor angiogenesis and vasculogenesis, which are vital aspects of osteosarcoma growth and behavior in vivo. Further, osteosarcoma cells themselves express relatively low levels of Notch ligand, making it likely that nonmalignant cells, especially endothelial cells and pericytes, are the major source of Notch activation in osteosarcoma tumors in vivo and in patients. As a result, Notch pathway expression is not expected to be uniform across a tumor but likely to be highest in those areas immediately adjacent to blood vessels. Therapeutic targeting of the Notch pathway is likewise expected to be complicated. Most pharmacologic approaches thus far have focused on inhibition of gamma secretase, a protease of the presenilin complex. This enzyme, however, has numerous other target proteins that would be expected to affect osteosarcoma behavior, including CD44, the WNT/β-catenin pathway, and Her-4. In addition, Notch plays a vital role in tissue and organ homeostasis in numerous systems, and toxicities, especially GI intolerance, have limited the effectiveness of gamma secretase inhibitors. New approaches are in development, and the downstream targets of Notch pathway signaling also may turn out to be good targets for therapy. In summary, a full understanding of the complex functions of Notch in osteosarcoma is only now unfolding, and this deeper knowledge will help position the field to better utilize novel therapies as they are developed.

摘要

Notch 通路已被描述为成骨肉瘤中的癌基因,但由于该复杂信号通路的所有成员在恶性细胞和肿瘤的非恶性成分中具有多种功能,因此将 Notch 简单地定义为癌基因或肿瘤抑制基因变得更加困难。Notch 通路操作引起的细胞自主行为可能因细胞系而异,但可包括增殖、迁移、侵袭、氧化应激抗性和与干性或肿瘤起始细胞相关标志物的表达变化。除了这些作用之外,Notch 信号还在调节肿瘤血管生成和血管发生中发挥重要作用,这是成骨肉瘤在体内生长和行为的重要方面。此外,成骨肉瘤细胞本身表达相对较低水平的 Notch 配体,因此,非恶性细胞,特别是内皮细胞和成纤维细胞,很可能是体内和患者中成骨肉瘤肿瘤中 Notch 激活的主要来源。因此,Notch 通路的表达预计不会在整个肿瘤中均匀,而可能在紧邻血管的区域最高。Notch 通路的治疗靶向同样预计会很复杂。迄今为止,大多数药物方法都集中在抑制 presenilin 复合物的蛋白酶γ-分泌酶上。然而,该酶具有许多其他预期会影响成骨肉瘤行为的靶蛋白,包括 CD44、WNT/β-连环蛋白通路和 Her-4。此外,Notch 在许多系统的组织和器官稳态中发挥着至关重要的作用,并且毒性,特别是胃肠道不耐受,限制了γ-分泌酶抑制剂的有效性。新的方法正在开发中,Notch 通路信号的下游靶标也可能成为治疗的良好靶标。总之,目前仅开始全面了解 Notch 在成骨肉瘤中的复杂功能,而这种更深入的了解将有助于为更好地利用新疗法做好准备,因为这些疗法正在开发中。

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