GATA6 in pancreatic cancer initiation and progression

被引:1
|
作者
Ma, Muyuan [1 ]
An, Jianhong [1 ]
Jiang, Tingting [1 ]
Xie, Keping [1 ]
机构
[1] South China Univ Technol, Ctr Pancreat Canc Res, Sch Med, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
GATA6; Inflammation; Molecular diagnosis; Pancreas; Targeted therapy; Tumorigenesis; TRANSCRIPTION FACTOR GATA-6; GENE; ADENOCARCINOMA; DIFFERENTIATION; CLASSIFICATION; EXPRESSION; REGULATOR; SUBTYPES; AMPLIFICATION; DEPENDENCY;
D O I
10.1016/j.gendis.2024.101353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic ductal adenocarcinoma (PDA) is a lethal malignancy characterized by insidious onset and lack of effective therapy. The molecular pathogenesis of PDA remains to be understood fully. Transcriptional factor GATA6 is an important transcriptional regulator in normal pancreas development, particularly in the initial specification and differentiation of the pancreas. Recent studies have linked pancreatic malignancy closely to GATA6. Increased levels of GATA6 expression enhance pancreatic cancer cell growth. GATA6 emerges as a lineage-specific oncogenic factor in PDA, augmenting the oncogenic phenotypes of PDA cells upon its overexpression. However, elevated GATA6 levels are correlated with well-differentiated tumors and a more favorable patient prognosis. Experimental evidence in genetic mouse models has revealed a tumor-suppressive role for GATA6. The circumstantial roles of GATA6 in pancreatic tumorigenesis remain to be defined. This review aims to elucidate recent advances in comprehending GATA6, emphasizing its crucial roles in both pancreas physiology and pathology. Special attention will be given to its involvement in PDA pathogenesis, exploring its potential as a novel biomarker and a promising therapeutic target for PDA. (c) 2024 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY license (http://creativecommons.org/
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页数:10
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