选择性糖皮质激素受体激活辅助治疗在癌症治疗中的应用

N. Sundahl, Dorien Clarisse, M. Bracke, F. Offner, W. V. Berghe, I. Beck
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引用次数: 28

摘要

尽管糖皮质激素的副作用和耐药性削弱了其长期使用,但糖皮质激素是急性和慢性炎症性疾病的主要治疗方法,在淋巴细胞恶性肿瘤的治疗方案中发挥重要作用,并作为辅助剂刺激各种实体肿瘤的治疗耐受性。糖皮质激素与指定的糖皮质激素受体(GR)结合,引发了大量的细胞特异性事件,包括治疗所需的效果,如细胞死亡,以及不希望的效果,包括化疗耐药,全身副作用和糖皮质激素耐药。在这种背景下,选择性GR激动剂和调节剂(SEGRAMs)已经开发出来,具有更有限的GR活性谱,有望进一步在抗炎和癌症治疗方面进行临床开发。迄今为止,对选择性GR调节剂在癌症治疗中的潜在益处的研究进展缓慢。我们的综述讨论了选择性GR激动剂和调节剂如何改善淋巴细胞恶性肿瘤、前列腺癌或乳腺癌的治疗方案。我们总结了我们目前的知识,并展望了该领域未来的发展方向。总之,我们的综述阐明了通过选择性GR靶向调节癌症的新治疗前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective glucocorticoid receptor-activating adjuvant therapy in cancer treatments
Although adverse effects and glucocorticoid resistance cripple their chronic use, glucocorticoids form the mainstay therapy for acute and chronic inflammatory disorders, and play an important role in treatment protocols of both lymphoid malignancies and as adjuvant to stimulate therapy tolerability in various solid tumors. Glucocorticoid binding to their designate glucocorticoid receptor (GR), sets off a plethora of cell-specific events including therapeutically desirable effects, such as cell death, as well as undesirable effects, including chemotherapy resistance, systemic side effects and glucocorticoid resistance. In this context, selective GR agonists and modulators (SEGRAMs) with a more restricted GR activity profile have been developed, holding promise for further clinical development in anti-inflammatory and potentially in cancer therapies. Thus far, the research into the prospective benefits of selective GR modulators in cancer therapy limped behind. Our review discusses how selective GR agonists and modulators could improve the therapy regimens for lymphoid malignancies, prostate or breast cancer. We summarize our current knowledge and look forward to where the field should move to in the future. Altogether, our review clarifies novel therapeutic perspectives in cancer modulation via selective GR targeting.
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