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Published on: December 26, 2016
Molecular networks of FOXP family: dual biologic functions, interplay with other molecules and clinical implications
Ju-Ha Kim1, Jisung Hwang1, Ji Hoon Jung1
1Cancer Molecular Target Herbal Research Lab, College of Korean Medicine, Kyung Hee university, 1 Hoegi-dong, Dongdaemun-gu, Seoul, 02447, Republic of Korea.
Abstract:
Though Forkhead box P (FOXP) transcription factors comprising of FOXP1, FOXP2, FOXP3 and FOXP4 are involved in the embryonic development, immune disorders and cancer progression, the underlying function of FOXP3 targeting CD4 + CD25+ regulatory T (Treg) cells and the dual roles of FOXP proteins as an oncogene or a tumor suppressor are unclear and controversial in cancers to date. Thus, the present review highlighted research history, dual roles of FOXP proteins as a tumor suppressor or an oncogene, their molecular networks with other proteins and noncoding RNAs, cellular immunotherapy targeting FOXP3, and clinical implications in cancer progression.
Insights
Forkhead box P (FOXP) proteins have dual roles in cancer, acting as oncogenes or tumor suppressors. This review clarifies FOXP3
Area of Science:
- Molecular Biology
- Immunology
- Oncology
Background:
- Forkhead box P (FOXP) transcription factors (FOXP1-4) are implicated in embryonic development, immune disorders, and cancer.
- The specific function of FOXP3 in CD4+CD25+ regulatory T (Treg) cells and the oncogenic or tumor-suppressive roles of FOXP proteins in cancer remain controversial.
Purpose of the Study:
- To review the historical research on FOXP proteins in cancer.
- To elucidate the dual roles of FOXP proteins as oncogenes or tumor suppressors.
- To explore their molecular interactions and clinical significance in cancer progression.
Main Methods:
- Literature review of research on FOXP transcription factors.
- Analysis of molecular networks involving FOXP proteins, other proteins, and noncoding RNAs.
- Examination of cellular immunotherapy targeting FOXP3.
- Review of clinical implications in cancer.
Main Results:
- FOXP proteins exhibit context-dependent functions, acting as either oncogenes or tumor suppressors in various cancers.
- FOXP3 plays a critical role in regulating CD4+CD25+ Treg cells, influencing the tumor microenvironment.
- Complex molecular networks involving FOXP proteins and noncoding RNAs modulate their functions.
Conclusions:
- Understanding the dual roles of FOXP proteins is crucial for cancer research and therapy.
- Targeting FOXP3 in cellular immunotherapy presents potential clinical applications for cancer treatment.
- Further research into FOXP protein networks can reveal novel therapeutic strategies for cancer progression.
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