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胰岛素样生长因子系统在软组织肉瘤中的作用:从生理病理学到靶向治疗方法

The role of insulin-like growth factor system in soft tissue sarcomas: from physiopathology to targeted therapeutic approaches.

作者信息

Zumkeller W

机构信息

Department of Hematology/Oncology Children's University Hospital Heidelberg Germany.

出版信息

Sarcoma. 1998;2(2):69-76. doi: 10.1080/13577149878028.

Abstract

Purpose/Results. Although surgical, chemo- and radiotherapeutic treatment regimens in patients with soft tissue sarcomas have constantly been refined over the past two decades, the survival rate for these patients is rather low.Discussion. There is a great need to investigate the mechanisms for oncogenesis and to identify the factors involved in malignant transformation in sarcomas. Among these factors, IGFs are thought to play a pivotal role as progression factors in various types of sarcomas. The dysregulation of the IGF-II synthesis, e.g. by loss of imprinting which occurs in most types of sarcomas, is a permissive effect through the suppression of cell death. In addition, cells that overexpress the type I IGF receptors are more susceptible to transformation by oncogenes. As TP53 suppresses the activity of IGF-II P3 and P4, as well as the type I IGF receptor promoter, mutations of TP53 in sarcomas may alternatively lead to the activation of these factors. Finally, the phenomenon of non-islet cell tumour hypoglycaemia that occurs in patients with sarcomas, and which is related to the secretion of IGF-II prohormones, is discussed. Future therapeutic strategies may be based upon the application of antibodies or antisense oligonucleotides directed against the type I IGF receptors, with the common goal of inducing apoptosis in sarcoma cells. Ultimately, these and other therapeutic approaches may lead to a better outcome in patients suffering from sarcoma.

摘要

目的/结果。尽管在过去二十年中软组织肉瘤患者的手术、化疗和放疗治疗方案不断完善,但这些患者的生存率仍然很低。讨论。迫切需要研究肿瘤发生机制并确定肉瘤恶性转化所涉及的因素。在这些因素中,胰岛素样生长因子(IGFs)被认为在各种类型的肉瘤中作为进展因子发挥关键作用。IGF-II合成的失调,例如通过大多数类型肉瘤中发生的印记丢失,是通过抑制细胞死亡产生的一种许可效应。此外,过度表达I型IGF受体的细胞更容易被癌基因转化。由于TP53抑制IGF-II P3和P4以及I型IGF受体启动子的活性,肉瘤中TP53的突变可能会导致这些因子的激活。最后,讨论了肉瘤患者中发生的与IGF-II前体激素分泌相关的非胰岛细胞瘤低血糖现象。未来的治疗策略可能基于应用针对I型IGF受体的抗体或反义寡核苷酸,共同目标是诱导肉瘤细胞凋亡。最终,这些及其他治疗方法可能会使肉瘤患者获得更好的治疗效果。

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