The roles and regulation of TBX3 in development and disease

被引:63
作者
Khan, Saif F. [1 ]
Damerell, Victoria [1 ]
Omar, Rehana [1 ]
Du Toit, Michelle [1 ]
Khan, Mohsin [1 ]
Maranyane, Hapiloe Mabaruti [1 ]
Mlaza, Mihlali [1 ]
Bleloch, Jenna [1 ]
Bellis, Claire [1 ]
Sahm, Bianca D. B. [1 ,2 ]
Peres, Jade [1 ]
ArulJothi, K. N. [1 ]
Prince, Sharon [1 ]
机构
[1] Univ Cape Town, Dept Human Biol, Fac Hlth Sci, Div Cell Biol, ZA-7925 Cape Town, South Africa
[2] Univ Sao Paulo, Dept Pharmacol, Inst Biomed Sci, BR-11030400 Sao Paulo, SP, Brazil
基金
新加坡国家研究基金会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
Transcription factor; T-box factors; TBX3; Heart development; Limb development; Mammary gland development; Lung development; Ulnar mammary syndrome; Obesity; Rheumatoid arthritis; Cancer; Signalling; Target genes; Co-factors; Stem cells; ULNAR-MAMMARY SYNDROME; BOX TRANSCRIPTION FACTOR; CELL SELF-RENEWAL; BREAST-CANCER; E-CADHERIN; SIGNALING PATHWAY; DOWNSTREAM TARGET; TUMOR-SUPPRESSOR; SONIC HEDGEHOG; RETINOIC ACID;
D O I
10.1016/j.gene.2019.144223
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
TBX3, a member of the ancient and evolutionary conserved T-box transcription factor family, is a critical developmental regulator of several structures including the heart, mammary glands, limbs and lungs. Indeed, mutations in the human TBX3 lead to ulnar mammary syndrome which is characterized by several clinical malformations including hypoplasia of the mammary and apocrine glands, defects of the upper limb, areola, dental structures, heart and genitalia. In contrast, TBX3 has no known function in adult tissues but is frequently overexpressed in a wide range of epithelial and mesenchymal derived cancers. This overexpression greatly impacts several hallmarks of cancer including bypass of senescence, apoptosis and anoikis, promotion of proliferation, tumour formation, angiogenesis, invasion and metastatic capabilities as well as cancer stem cell expansion. The debilitating consequences of having too little or too much TBX3 suggest that its expression levels need to be tightly regulated. While we have a reasonable understanding of the mutations that result in low levels of functional TBX3 during development, very little is known about the factors responsible for the overexpression of TBX3 in cancer. Furthermore, given the plethora of oncogenic processes that TBX3 impacts, it must be regulating several target genes but to date only a few have been identified and characterised. Interestingly, while there is compelling evidence to support oncogenic roles for TBX3, a few studies have indicated that it may also have tumour suppressor functions in certain contexts. Together, the diverse functional elasticity of TBX3 in development and cancer is thought to involve, in part, the protein partners that it interacts with and this area of research has recently received some attention. This review provides an insight into the significance of TBX3 in development and cancer and identifies research gaps that need to be explored to shed more light on this transcription factor.
引用
收藏
页数:17
相关论文
共 196 条
[11]   Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome [J].
Bamshad, M ;
Lin, RC ;
Law, DJ ;
Watkins, WS ;
Krakowiak, PA ;
Moore, ME ;
Franceschini, P ;
Lala, R ;
Holmes, LB ;
Gebuhr, TC ;
Bruneau, BG ;
Schinzel, A ;
Seidman, JG ;
Seidman, CE ;
Jorde, LB .
NATURE GENETICS, 1997, 16 (03) :311-315
[12]   New Insights into the Mechanisms of Embryonic Stem Cell Self-Renewal under Hypoxia: A Multifactorial Analysis Approach [J].
Barbosa, Helder S. C. ;
Fernandes, Tiago G. ;
Dias, Tiago P. ;
Diogo, Maria Margarida ;
Cabral, Joaquim M. S. .
PLOS ONE, 2012, 7 (06)
[13]  
Barnum KJ, 2014, METHODS MOL BIOL, V1170, P29, DOI 10.1007/978-1-4939-0888-2_2
[14]   CYTOLOGICAL DEMONSTRATION OF CLONAL NATURE OF SPLEEN COLONIES DERIVED FROM TRANSPLANTED MOUSE MARROW CELLS [J].
BECKER, AJ ;
TILL, JE ;
MCCULLOCH, EA .
NATURE, 1963, 197 (486) :452-&
[15]   Dynamic expression of Tbx2 and Tbx3 in developing mouse pancreas [J].
Begum, Salma ;
Papaioannou, Virginia E. .
GENE EXPRESSION PATTERNS, 2011, 11 (08) :476-483
[16]   E2F and Ras Synergize in Transcriptionally Activating p14ARF Expression [J].
Berkovich, Eli ;
Lamed, Yocheved ;
Ginsberg, Doron .
CELL CYCLE, 2003, 2 (02) :127-133
[17]   Stratification based on methylation of TBX2 and TBX3 into three molecular grades predicts progression in patients with pTa-bladder cancer [J].
Beukers, Willemien ;
Kandimalla, Raju ;
Masius, Roy G. ;
Vermeij, Marcel ;
Kranse, Ries ;
van Leenders, Geert J. L. H. ;
Zwarthoff, Ellen C. .
MODERN PATHOLOGY, 2015, 28 (04) :515-522
[18]   Sox4 mediates Tbx3 transcriptional regulation of the gap junction protein Cx43 [J].
Boogerd, C. J. J. ;
Wong, L. Y. E. ;
van den Boogaard, M. ;
Bakker, M. L. ;
Tessadori, F. ;
Bakkers, J. ;
't Hoen, P. A. C. ;
Moorman, A. F. ;
Christoffels, V. M. ;
Barnett, P. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (23) :3949-3961
[19]   Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43 [J].
Boogerd, Kees-Jan ;
Wong, L. Y. Elaine ;
Christoffels, Vincent M. ;
Klarenbeek, Meinke ;
Ruijter, Jan M. ;
Moorman, Antoon F. M. ;
Barnett, Phil .
CARDIOVASCULAR RESEARCH, 2008, 78 (03) :485-493
[20]   Oncogenic B-RAFV600E Signaling Induces the T-Box3 Transcriptional Repressor to Repress E-Cadherin and Enhance Melanoma Cell Invasion [J].
Boyd, Suzanah C. ;
Mijatov, Branka ;
Pupo, Gulietta M. ;
Tran, Sieu L. ;
Gowrishankar, Kavitha ;
Shaw, Heather M. ;
Goding, Colin R. ;
Scolyer, Richard A. ;
Mann, Graham J. ;
Kefford, Richard F. ;
Rizos, Helen ;
Becker, Therese M. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2013, 133 (05) :1269-1277