RADIOSENSITIZATION OF CANCER STEM CELLS: TARGETING TGFβ, NOTCH OR TELOMERASE TO IMPROVE TUMOR RESPONSE O RADIOTHERAPY

I. Fernandez-Garcia
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Abstract

Radiation resistant cancer stem cells are the main reason for treatment failure and tumor recurrence after cancer radiotherapy. Increasing biological evidences demonstrate that these cells possess the capacity to repair radiation induced DNA damage, protect themselves from radiation derived reactive oxygen species, survive and proliferate after several fractions of radiotherapy and finally, repopulate the heterogeneity of the tumor. Thus, targeting and eliminating these cells should be necessary to achieve cancer cure in radiotherapy. Three major approaches that specifically target radioresistant cancer stem cells have been recently investigated. First, inhibition of TGFβ, a major mediator of the tissue response to radiation, has been shown to induce radiosensitization of cancer stem cells by targeting the DNA damage response mechanism. Second, by preventing Notch activation during fractionated radiotherapy, cancer stem cells were depleted from their ability to repopulate the tumor after radiation. Finally, telomerase activity inhibitors have shown to specifically decrease the cancer stem cell population after radiotherapy. In the present review, we evaluate these radiosentitizing approaches and their possible effects when combined with fractionated radiotherapy as they promise to be a powerful tool in the battle against this cancer.
肿瘤干细胞的放射增敏:靶向tgfβ、缺口或端粒酶以改善肿瘤对放疗的反应
耐辐射肿瘤干细胞是癌症放疗后治疗失败和肿瘤复发的主要原因。越来越多的生物学证据表明,这些细胞具有修复辐射诱导的DNA损伤的能力,保护自己免受辐射衍生的活性氧的伤害,在几次放射治疗后存活和增殖,并最终重新填充肿瘤的异质性。因此,靶向和消除这些细胞对于实现放射治疗中的癌症治愈是必要的。最近研究了三种专门针对放射耐药癌症干细胞的主要方法。首先,TGFβ(组织对辐射反应的主要介质)的抑制已被证明可以通过靶向DNA损伤反应机制诱导癌症干细胞的放射致敏。其次,通过在分割放疗期间阻止Notch激活,癌症干细胞在放疗后失去了重新填充肿瘤的能力。最后,端粒酶活性抑制剂已经显示出特异性地减少放射治疗后的癌症干细胞数量。在目前的回顾中,我们评估了这些放射致敏方法及其与分步放射治疗相结合时可能产生的效果,因为它们有望成为对抗这种癌症的有力工具。
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