Author
Listed:
- Wei Song
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Wenjie Liu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Hong Zhao
(Cancer Hospital & Institute, Chinese Academy of Medical Sciences)
- Shangze Li
(College of Life Sciences, Wuhan University)
- Xin Guan
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Jianming Ying
(Cancer Hospital & Institute, Chinese Academy of Medical Sciences)
- Yefan Zhang
(Cancer Hospital & Institute, Chinese Academy of Medical Sciences)
- Fei Miao
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Mengmeng Zhang
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Xiaoxia Ren
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Xiaolu Li
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Fan Wu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Yuechao Zhao
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Yuanyuan Tian
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Wenming Wu
(Peking Union Medical College Hospital, Chinese Academy of Medical Sciences)
- Jun Fu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Junbo Liang
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Wei Wu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Changzheng Liu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Jia Yu
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Shudong Zong
(National Research Institute for Family Planning, WHO Collaboration Center of Human Reproduction)
- Shiying Miao
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
- Xiaodong Zhang
(College of Life Sciences, Wuhan University)
- Linfang Wang
(State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, Peking Union Medical College)
Abstract
Rhomboid proteins perform a wide range of important functions in a variety of organisms. Recent studies have revealed that rhomboid proteins are involved in human cancer progression; however, the underlying molecular mechanism remains largely unclear. Here we show that RHBDD1, a rhomboid intramembrane serine protease, is highly expressed and closely associated with survival in patients with colorectal cancer. We observe that inactivation of RHBDD1 decreases tumor cell growth. Further studies show that RHBDD1 interacts with proTGFα and induces the ADAM-independent cleavage and secretion of proTGFα. The secreted TGFα further triggers the activation of the EGFR/Raf/MEK/ERK signalling pathway. Finally, the positive correlation of RHBDD1 expression with the EGFR/Raf/MEK/ERK signalling pathway is further corroborated in a murine model of colitis-associated colorectal cancer. These findings provide evidence of a growth-promoting role for RHBDD1 in colorectal cancer and may aid the development of tumor biomarkers or antitumor therapeutics.
Suggested Citation
Wei Song & Wenjie Liu & Hong Zhao & Shangze Li & Xin Guan & Jianming Ying & Yefan Zhang & Fei Miao & Mengmeng Zhang & Xiaoxia Ren & Xiaolu Li & Fan Wu & Yuechao Zhao & Yuanyuan Tian & Wenming Wu & Jun, 2015.
"Rhomboid domain containing 1 promotes colorectal cancer growth through activation of the EGFR signalling pathway,"
Nature Communications, Nature, vol. 6(1), pages 1-13, November.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9022
DOI: 10.1038/ncomms9022
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