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Roles of transducin-like enhancer of split (TLE) family proteins in tumorigenesis and immune regulation.
Yu, Guiping; Chen, Yiqi; Hu, Yuwen; Zhou, Yan; Ding, Xiaoling; Zhou, Xiaorong.
Afiliación
  • Yu G; Department of Immunology, Nantong University, School of Medicine, Nantong, China.
  • Chen Y; Department of Cardiothoracic Surgery, The Affiliated Jiangyin Hospital of Nantong University, Jiangyin, China.
  • Hu Y; Department of Immunology, Nantong University, School of Medicine, Nantong, China.
  • Zhou Y; Department of Immunology, Nantong University, School of Medicine, Nantong, China.
  • Ding X; Department of Periodontology, The Affiliated Nantong Stomatological Hospital of Nantong University, Nantong, China.
  • Zhou X; Department of Gastroenterology, The Affiliated Hospital of Nantong University, Nantong, China.
Front Cell Dev Biol ; 10: 1010639, 2022.
Article en En | MEDLINE | ID: mdl-36438567
ABSTRACT
Mammalian transducin-like enhancer of split family proteins (TLEs) are homologous to Drosophila Groucho (Gro) and are essential transcriptional repressors. Seven TLE family members, TLE1-7, have been identified to date. These proteins do not bind DNA directly; instead, they bind a set of transcription factors and thereby inhibit target gene expression. Loss of TLEs in mice usually leads to defective early development; however, TLE functions in developmentally mature cells are unclear. Recent studies have revealed that TLEs are dysregulated in certain human cancer types and may function as oncogenes or tumor suppressors in different contexts. TLE levels also affect the efficacy of cancer treatments and the development of drug resistance. In addition, TLEs play critical roles in the development and function of immune cells, including macrophages and lymphocytes. In this review, we provide updates on the expression, function, and mechanism of TLEs; discuss the roles played by TLEs in tumorigenesis and the inflammatory response; and elaborate on several TLE-associated signaling pathways, including the Notch, Wnt, and MAPK pathways. Finally, we discuss potential strategies for targeting TLEs in cancer therapy.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Cell Dev Biol Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Cell Dev Biol Año: 2022 Tipo del documento: Article País de afiliación: China