AI Article Synopsis

  • CREB is a transcription factor involved in cell responses to environmental stimuli, impacting processes like proliferation and survival, particularly in leukemia.
  • Studies suggest that CREB activation can enhance resistance to ionizing radiation (IR) therapy in cancer cells, promoting their survival under low-dose radiation.
  • The mini-review aims to explore the dual roles of CREB - both as a promoter of cell survival and a potential pro-apoptotic factor - in order to identify biomarkers for personalized cancer treatment following IR therapy.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418225PMC
http://dx.doi.org/10.3389/fonc.2017.00076DOI Listing

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