2. Academic Validation
  3. Lysosomal EGFR acts as a Rheb-GEF independent of its kinase activity to activate mTORC1

Lysosomal EGFR acts as a Rheb-GEF independent of its kinase activity to activate mTORC1

  • Cell Res. 2025 Jul;35(7):497-509. doi: 10.1038/s41422-025-01110-x.
Xiaobo He # 1,  Qiu-Xia Wang # 1,  Denghui Wei # 2,  Yujie Lin # 1,  Xia Zhang # 1,  Yuanzhong Wu 1,  Xuexia Qian 3,  Zhihao Lin 3,  Beibei Xiao 1,  Qinxue Wu 4,  Zhen Wang 4,  Fengtao Zhou 5,  Zhihao Wei 1 6,  Jingxuan Wang 1,  Run Gong 1,  Ruhua Zhang 1,  Qingling Zhang 7,  Ke Ding 8 9,  Song Gao 10 11,  Tiebang Kang 12
Affiliations

Affiliations

  • 1 Sun Yat-sen University Cancer Center, Guangdong Provincial Clinical Research Center for Cancer, State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China.
  • 2 Sun Yat-sen University Cancer Center, Guangdong Provincial Clinical Research Center for Cancer, State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China. weidh@sysucc.org.cn.
  • 3 Department of Pathology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
  • 4 State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.
  • 5 International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development, Ministry of Education (MoE) of People's Republic of China, College of Pharmacy, Jinan University, Guangzhou, Guangdong, China.
  • 6 Department of Oncology Radiotherapy, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, China.
  • 7 Department of Pathology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China. zhangqingling@gdph.org.cn.
  • 8 State Key Laboratory of Chemical Biology, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China. dingk@sioc.ac.cn.
  • 9 International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development, Ministry of Education (MoE) of People's Republic of China, College of Pharmacy, Jinan University, Guangzhou, Guangdong, China. dingk@sioc.ac.cn.
  • 10 Sun Yat-sen University Cancer Center, Guangdong Provincial Clinical Research Center for Cancer, State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China. gaosong@sysucc.org.cn.
  • 11 Integrated Traditional Chinese and Western Medicine Research Center, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China. gaosong@sysucc.org.cn.
  • 12 Sun Yat-sen University Cancer Center, Guangdong Provincial Clinical Research Center for Cancer, State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China. kangtb@sysucc.org.cn.
  • # Contributed equally.
PMID: 40259053 DOI: 10.1038/s41422-025-01110-x
Abstract

Oncogenic mutations in EGFR often result in EGF-independent constitutive activation and aberrant trafficking and are associated with several human malignancies, including non-small cell lung Cancer. A major consequence of EGFR mutations is the activation of the mechanistic target of rapamycin complex 1 (mTORC1), which requires EGFR kinase activity and downstream PI3K/Akt signaling, resulting in increased cell proliferation. However, recent studies have elucidated kinase-independent roles of EGFR in cell survival and Cancer progression. Here, we report a cis mTORC1 activation function of EGFR that is independent of its kinase activity. Our results reveal that lysosomal localization of EGFR is critical to mTORC1 activation, where EGFR physically binds Rheb, acting as a guanine exchange factor (GEF) for Rheb, with its Glu804 serving as a potential glutamic finger. Genetic knock-in of EGFR-E804K in cells reduces the level of GTP-bound Rheb, and significantly suppresses mTORC1 activation, cell proliferation and tumor growth. Different tyrosine kinase inhibitors exhibit distinct effects on EGFR-induced mTORC1 activation, with afatinib, which additionally blocks EGFR's GEF activity, causing a much greater suppression of mTORC1 activation and cell growth, and erlotinib, which targets only kinase activity, resulting in only a slight decrease. Moreover, a novel small molecule, BIEGi-1, was designed to target both the Rheb-GEF and kinase activities of EGFR, and shows a strong inhibitory effect on the viability of cells harboring EGFR mutants. These findings unveil a fundamental event in cell growth and suggest a promising strategy against cancers with EGFR mutations.

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