Butt Danial Qasim, Harun Masitah Hayati, Che Jalil Nur Asyilla, Shamsuddin Shazana Hilda, Jaafar Saidi, Ahmad Basaruddin
Oral Medicine and Oral Pathology Unit, School of Dental Sciences, Universiti Sains Malaysia, Kubang Kerian, MYS.
Pathology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, MYS.
Cureus. 2024 Jun 26;16(6):e63216. doi: 10.7759/cureus.63216. eCollection 2024 Jun.
Interferon-stimulated genes (ISGs), whose production is triggered by interferons, are known to defend the host from pathogenic and cancer-specific antigens, one of which is by inducing apoptosis in infected or mutated cells. It has been reported recently that specific ISGs aid cancer cells in evading immunosurveillance and inflammatory cells by inhibiting the apoptosis process. This report reviewed four apoptosis-regulating ISG proteins: interferon-stimulated gene 15 (ISG15), interferon alpha-inducible protein 27 (IFI27), interferon alpha-inducible protein 6 (IFI6), and radical S-adenosyl methionine domain containing 2 (RSAD2), demonstrating anti-apoptosis function, and considered them protumorigenic.
干扰素刺激基因(ISGs)的产生由干扰素触发,已知其可保护宿主免受致病性和癌症特异性抗原的侵害,其中一种方式是诱导感染或突变细胞凋亡。最近有报道称,特定的ISGs通过抑制凋亡过程帮助癌细胞逃避免疫监视和炎性细胞。本报告综述了四种调节凋亡的ISG蛋白:干扰素刺激基因15(ISG15)、干扰素α诱导蛋白27(IFI27)、干扰素α诱导蛋白6(IFI6)和含2的自由基S-腺苷甲硫氨酸结构域(RSAD2),这些蛋白具有抗凋亡功能,并被认为具有促肿瘤作用。