RIPK1 Binds MCU to Mediate Induction of Mitochondrial Ca2+ Uptake and Promotes Colorectal Oncogenesis

The receptor-interacting protein kinase 1 (RIPK1) is an essential signaling molecule in pathways for cell survival, apoptosis, and necroptosis. We report here that RIPK1 is upregulated in human colorectal cancer and promotes cell proliferation when overexpressed in a colon cancer cell line. RIPK1 in...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2018-06, Vol.78 (11), p.2876-2885
Hauptverfasser: Zeng, Fanxin, Chen, Xiao, Cui, Weiyi, Wen, Wei, Lu, Fujian, Sun, Xueting, Ma, Dongwei, Yuan, Ye, Li, Zezhong, Hou, Ning, Zhao, Hong, Bi, Xinyu, Zhao, Jianjun, Zhou, Jianguo, Zhang, Yan, Xiao, Rui-Ping, Cai, Jianqiang, Zhang, Xiuqin
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Sprache:eng
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Zusammenfassung:The receptor-interacting protein kinase 1 (RIPK1) is an essential signaling molecule in pathways for cell survival, apoptosis, and necroptosis. We report here that RIPK1 is upregulated in human colorectal cancer and promotes cell proliferation when overexpressed in a colon cancer cell line. RIPK1 interacts with mitochondrial Ca2+ uniporter (MCU) to promote proliferation by increasing mitochondrial Ca2+ uptake and energy metabolism. The ubiquitination site of RIPK1 (RIPK1-K377) was critical for this interaction with MCU and function in promoting cell proliferation. These findings identify the RIPK1-MCU pathway as a promising target to treat colorectal cancer. Significance: RIPK1-mediated cell proliferation through MCU is a central mechanism underlying colorectal cancer progression and may prove to be an important therapeutic target for colorectal cancer treatment. Cancer Res; 78(11); 2876–85. ©2018 AACR.
ISSN:0008-5472
1538-7445
DOI:10.1158/0008-5472.CAN-17-3082