생화학분자생물학회입니다.
MAP4K signaling pathways in cancer: roles, mechanisms and therapeutic opportunities
작성자
Gayoung Seo작성일자
2025-12-24조회수
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Name: Gayoung Seo ( gayoungs@sch.ac.kr ) | |
| 2024- | Assistant professor in Department of Integrated Medical Bioscience Soonchunhyang Institute of Medi-bio Science (SIMS), Soonchunhyang University, Republic of Korea | |
| 2023-2024 | Associate specialist in Department of developmental and cell biology University of California, Irvine, CA, United states | |
| 2018-2023 | Postdoctoral fellow in Department of developmental and cell biology University of California, Irvine, CA, United states | |
| -2018 | Ph.D. in Department of Medicine Jeju National University, Republic of Korea | |
MAP4K signaling pathways in cancer: roles, mechanisms and therapeutic opportunities
The MAP4K family, consisting of seven kinases (MAP4K1–7), plays crucial roles in regulating diverse cellular processes, including proliferation, differentiation, migration and apoptosis. Recent studies have highlighted their involvement in multiple signaling pathways such as mitogen-activated protein kinase, Jun N-terminal kinase and Hippo, implicating them in conditions such as cancer, autoimmune and metabolic disorders and neurodegenerative diseases. Notably, MAP4K proteins have demonstrated significant roles in cancer development and progression, including tumor growth, metastasis and immune modulation. Here we summarize current insights into the roles of individual MAP4K members in cancer and other diseases, emphasizing their distinct and overlapping functions within key signaling networks. Furthermore, we discuss the therapeutic potential of targeting MAP4K family members for cancer treatment. These kinases represent promising targets for developing novel therapies for cancer and related diseases. Future research is essential to clarify the specific molecular mechanisms of MAP4K proteins in cancer and to explore their broader relevance in health and disease.
Exp Mol Med. 2025 Oct;57(10):2148-2156. doi: 10.1038/s12276-025-01544-8.
https://pubmed.ncbi.nlm.nih.gov/41034525/