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CDK5RAP3 Participates in Autophagy Regulation and Is Downregulated in Renal Cancer

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单位: [1]Department of Urology, Beijing Friendship Hospital, Capital Medical University, Beijing, China [2]Department of Clinical Laboratory, Peking University People’s Hospital, Beijing, China
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Renal cancer is one of the most common malignant urological tumors; however, its diagnosis and treatment are not well established. In the present study, we identified that CDK5 regulatory subunit-associated protein 3 (CDK5RAP3), a putative tumor suppressor in many cancers, was downregulated in renal cancer tissues. Through loss- and gain-of-function experiments, we observed that the action of CDK5RAP3 in renal cancer cells was different in Caki-1 and 769-P cell lines. Knockdown of endogenous CDK5RAP3 in Caki-1 slightly increased cell viability, whereas overexpression of CDK5RAP3 in 769-P cells inhibited cell viability. In addition, we observed that CDK5RAP3 participated in the regulation of autophagy in renal cancer. Knockdown of CDK5RAP3 induced significant inhibition of autophagy in Caki-1 cells but not in 769-P cells. In contrast, overexpression of CDK5RAP3 significantly activated autophagy in 769-P cells, as evidenced by increased LC3-II levels. However, the LC3-II could not be altered by CDK5RAP3 overexpression in Caki-1 cells. These findings demonstrated that CDK5RAP3 is downregulated in renal cancer and may be associated with autophagy.

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出版当年[2018]版:
大类 | 3 区 医学
小类 | 3 区 生物工程与应用微生物 3 区 病理学 4 区 遗传学 4 区 医学:研究与实验
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Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Q2 GENETICS & HEREDITY Q2 MEDICINE, RESEARCH & EXPERIMENTAL Q2 PATHOLOGY
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第一作者单位: [1]Department of Urology, Beijing Friendship Hospital, Capital Medical University, Beijing, China
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