Atonal bHLH transcription factor 1 is an important factor for maintaining the balance of cell proliferation and differentiation in tumorigenesis

被引:10
|
作者
Fu, Ying [1 ]
Yuan, Sha-Sha [1 ]
Zhang, Li-Jie [1 ]
Ji, Zhi-Li [1 ]
Quan, Xiao-Jiang [1 ,2 ]
机构
[1] Capital Med Univ, Lu He Hosp, Endocrinol Ctr, Key Lab Diabet Prevent & Res, 82 XinHua South Rd, Beijing 101149, Peoples R China
[2] Hop La Pitie Salpetriere, Lab Brain Dev, Inst Cerveau & Moelle Epiniere, F-75013 Paris, France
关键词
tumorigenesis; atonal bHLH transcription factor 1; proliferation; differentiation; COLON-CANCER CELLS; PRONEURAL GENE; MERKEL CELLS; BETA-CATENIN; HOMOLOG; NEUROENDOCRINE DIFFERENTIATION; INHIBITS PROLIFERATION; SECRETASE INHIBITORS; COLORECTAL-CANCER; SIGNALING PATHWAY;
D O I
10.3892/ol.2020.11833
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Establishing the link between cellular processes and oncogenesis may aid the elucidation of targeted and effective therapies against tumor cell proliferation and metastasis. Previous studies have investigated the mechanisms involved in maintaining the balance between cell proliferation, differentiation and migration. There is increased interest in determining the conditions that allow cancer stem cells to differentiate as well as the identification of molecules that may serve as novel drug targets. Furthermore, the study of various genes, including transcription factors, which serve a crucial role in cellular processes, may present a promising direction for future therapy. The present review described the role of the transcription factor atonal bHLH transcription factor 1 (ATOH1) in signaling pathways in tumorigenesis, particularly in cerebellar tumor medulloblastoma and colorectal cancer, where ATOH1 serves as an oncogene or tumor suppressor, respectively. Additionally, the present review summarized the associated therapeutic interventions for these two types of tumors and discussed novel clinical targets and approaches.
引用
收藏
页码:2595 / 2605
页数:11
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