RIO 激酶在癌症研究和治疗中的作用

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Reviews on cancer Pub Date : 2024-04-09 DOI:10.1016/j.bbcan.2024.189100
Morteza Ghandadi , Albert Dobi , Sanjay V. Malhotra
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引用次数: 0

摘要

包括 RIOK1、RIOK2 和 RIOK3 在内的 RIO(右侧开放阅读框)激酶家族因其在核糖体生物发生过程中的作用而闻名。RIO 激酶的功能障碍与恶性肿瘤有关,包括急性髓性白血病、胶质瘤、乳腺癌、结直肠癌、肺癌和前列腺癌,这表明 RIO 激酶是癌症的潜在靶点。体外、体内和临床研究表明,RIO 激酶在各种类型的癌症中过度表达,这表明它们在肿瘤发生尤其是转移过程中发挥着重要作用。在恶性肿瘤中,RIO 激酶参与了促癌通路,包括 AKT/mTOR、RAS、p53 和 NF-κB 以及细胞周期调控。在此,我们回顾了 RIO 激酶在癌症发展中的作用,强调其作为治疗靶点的潜力,并鼓励进一步开发和研究癌症抑制剂。
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A role for RIO kinases in the crosshair of cancer research and therapy

RIO (right open reading frame) family of kinases including RIOK1, RIOK2 and RIOK3 are known for their role in the ribosomal biogenesis. Dysfunction of RIO kinases have been implicated in malignancies, including acute myeloid leukemia, glioma, breast, colorectal, lung and prostatic adenocarcinoma suggesting RIO kinases as potential targets in cancer. In vitro, in vivo and clinical studies have demonstrated that RIO kinases are overexpressed in various types of cancers suggesting important roles in tumorigenesis, especially in metastasis. In the context of malignancies, RIO kinases are involved in cancer-promoting pathways including AKT/mTOR, RAS, p53 and NF-κB and cell cycle regulation. Here we review the role of RIO kinases in cancer development emphasizing their potential as therapeutic target and encouraging further development and investigation of inhibitors in the context of cancer.

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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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