Targeting deubiquitinase USP28 for cancer therapy

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作者
Xiaofang Wang
Zhiyi Liu
Li Zhang
Zhaozhi Yang
Xingxing Chen
Jurui Luo
Zhirui Zhou
Xin Mei
Xiaoli Yu
Zhimin Shao
Yan Feng
Shen Fu
Zhen Zhang
Dongping Wei
Lijun Jia
Jinli Ma
Xiaomao Guo
机构
[1] Fudan University Shanghai Cancer Center,Department of Radiation Oncology
[2] Fudan University,Department of Oncology, Shanghai Medical College
[3] The University of Texas MD Anderson Cancer Center,Department of Head and Neck Surgery
[4] Fudan University Shanghai Cancer Center,Department of Breast Surgery
[5] The First Hospital of Nanjing,Department of Oncology
[6] Shanghai University of Traditional Chinese Medicine,Cancer Institute, Longhua Hospital
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摘要
As one of the most important post-translational modifications, ubiquitination plays versatile roles in cancer-related pathways, and is involved in protein metabolism, cell-cycle progression, apoptosis, and transcription. Counteracting the activities of the E3 ligases, the deubiquitylating enzymes have been suggested as another important mechanism to modulate the ubiquitination process, and are implicated in cancer as well. In this article, we review the emerging roles of USP28 in cancer pathways as revealed by recent studies. We discuss the major mechanisms by which USP28 is involved in the cancer-related pathways, whereby USP28 regulates physiological homeostasis of ubiquitination process, DNA-damage response, and cell cycle during genotoxic stress. We further review the studies where USP28 was targeted for treating multiples cancers including non-small cell lung cancer, breast cancer, intestinal cancers, gliomas, and bladder cancer. As a result, the clinical significance of targeting USP28 for cancer therapy merits further exploration and demonstration.
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