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Immediate early response gene 5 protein (IER5) is a 327-amino-acid transcription factor predominantly localized to the nucleus, quickly induced by stressors such as radiation, oncogenic signals, and heat shock[5][1][2][3]. IER5 regulates the cell cycle, inhibits cell proliferation by downregulating CDC25B, and mediates survival and stress responses via interaction with phosphatase PP2A and the heat shock factor HSF1[5][7]. It facilitates repair of DNA double-strand breaks through non-homologous end joining, and interacts with key DNA repair proteins PARP1 and Ku70[1]. IER5 is frequently upregulated in cancer types, modulating treatment responses and serving as a biomarker for radiation exposure and cancer prognosis[4][6][1]. Modulation of IER5 levels can influence therapeutic effects in cancer and its inhibition may present new therapeutic strategies[1][4].
Drugs targeting PARP1 (e.g., olaparib) may affect IER5-mediated DNA damage repair, potentially enhancing therapeutic effects/response in cancer
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