D'Auria Francesca, Centurione Lucia, Centurione Maria Antonietta, Angelini Antonio, Di Pietro Roberta
Department of Cardiac and Vascular Surgery, Campus Bio-Medico University of Rome, Rome, Italy.
Department of Medicine and Ageing Sciences, G. d'Annunzio University, Chieti, Italy.
Front Oncol. 2017 May 5;7:76. doi: 10.3389/fonc.2017.00076. eCollection 2017.
Cyclic AMP response element binding (CREB) protein is a member of the CREB/activating transcription factor (ATF) family of transcription factors that play an important role in the cell response to different environmental stimuli leading to proliferation, differentiation, apoptosis, and survival. A number of studies highlight the involvement of CREB in the resistance to ionizing radiation (IR) therapy, demonstrating a relationship between IR-induced CREB family members' activation and cell survival. Consistent with these observations, we have recently demonstrated that CREB and ATF-1 are expressed in leukemia cell lines and that low-dose radiation treatment can trigger CREB activation, leading to survival of erythro-leukemia cells (K562). On the other hand, a number of evidences highlight a proapoptotic role of CREB following IR treatment of cancer cells. Since the development of multiple mechanisms of resistance is one key problem of most malignancies, including those of hematological origin, it is highly desirable to identify biological markers of responsiveness/unresponsiveness useful to follow-up the individual response and to adjust anticancer treatments. Taking into account all these considerations, this mini-review will be focused on the involvement of CREB/ATF family members in response to IR therapy, to deepen our knowledge of this topic, and to pave the way to translation into a therapeutic context.
环磷酸腺苷反应元件结合(CREB)蛋白是CREB/激活转录因子(ATF)转录因子家族的成员,该家族在细胞对导致增殖、分化、凋亡和存活的不同环境刺激的反应中起重要作用。许多研究强调了CREB在抗电离辐射(IR)治疗中的作用,证明了IR诱导的CREB家族成员激活与细胞存活之间的关系。与这些观察结果一致,我们最近证明CREB和ATF-1在白血病细胞系中表达,低剂量辐射治疗可触发CREB激活,从而导致红白血病细胞(K562)存活。另一方面,大量证据表明,IR治疗癌细胞后,CREB具有促凋亡作用。由于多种耐药机制的形成是大多数恶性肿瘤(包括血液系统恶性肿瘤)的一个关键问题,因此非常需要确定有助于跟踪个体反应和调整抗癌治疗的反应性/无反应性生物标志物。考虑到所有这些因素,本综述将聚焦于CREB/ATF家族成员在IR治疗反应中的作用,以加深我们对该主题的了解,并为转化为治疗背景铺平道路。