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MC1R contributes to ferroptosis resistance and tumor aggressiveness in colorectal cancer by activating Notch signaling

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成果类型:
期刊论文
作者:
Zeng, Xiangwei;Jiang, Lujian;Li, Huili;Wang, Jiamou;He, Xuan
通讯作者:
He, X
作者机构:
[Zeng, Xiangwei; Wang, Jiamou] Wuhan Polytech Univ, Coll Med & Hlth Sci, Wuhan 430000, Hubei, Peoples R China.
[Jiang, Lujian] Tianjin Acad Tradit Chinese Med, Affiliated Hosp, Tianjin 300120, Peoples R China.
[Li, Huili] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Thorac Surg, Wuhan 430022, Hubei, Peoples R China.
[He, Xuan] Wuhan Univ, Renmin Hosp, Wuhan 430000, Hubei, Peoples R China.
通讯机构:
[He, X ] W
Wuhan Univ, Renmin Hosp, Wuhan 430000, Hubei, Peoples R China.
语种:
英文
期刊:
Cancer Gene Therapy
ISSN:
0929-1903
年:
2025
页码:
1-13
基金类别:
This research was funded by the Natural Science Foundation of Hubei Province, grant number 2022CFB138 to Huili Li; by the Hubei Key Laboratory of Regenerative Medicine and Multi-disciplinary Translational Research, grant number 2023zsyx003 to Huili Li; by the Hubei Key Laboratory of Biological Targeted Therapy, Union Hospital, Tongji Medical College,Huazhong University of Science and Technology, grant number 202415 to Huili Li; by the Natural Science Foundation of Hubei Province, grant number 2025AFB304 to Xiangwei Zeng.
机构署名:
本校为第一机构
院系归属:
医学与健康学院
摘要:
Ferroptosis, a form of iron-dependent cell death, is emerging as a potential therapeutic target due to its ability to inhibit tumor growth and enhance immune responses. However, the mechanisms regulating ferroptosis and tumor metastasis, particularly in colorectal cancer (CRC), remain poorly understood. In this study, bioinformatics analysis identified MC1R as a key regulator of ferroptosis-related genes. In vitro experiments showed MC1R overexpression in CRC cell lines promotes cell proliferation and migration while inhibiting ferroptosis via downregulating ACSL4 expression, with opposite eff...

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