RUNX1: A Regulator of NF-κB Signaling in Pulmonary Diseases

被引:67
作者
Tang, Xiaoju [1 ]
Sun, Ling [2 ]
Wang, Gang [1 ]
Chen, Bojiang [1 ]
Luo, Fengming [1 ]
机构
[1] Sichuan Univ, West China Hosp, Res Ctr Regenerat Med, Dept Pulm & Crit Care Med, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Res Ctr Regenerat Med, Lab Cardiovasc Dis, Chengdu, Sichuan, Peoples R China
关键词
RUNX1; NF-kappa B; IKK; P50; lung; pulmonary inflammation; ACUTE MYELOID-LEUKEMIA; STEM-CELL BIOLOGY; GRANULOCYTIC DIFFERENTIATION; BETA-SUBUNIT; GENE AML1; EXPRESSION; TRANSCRIPTION; DOMAIN; HEMATOPOIESIS; PROMOTER;
D O I
10.2174/1389203718666171009111835
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
Runt-related transcription factor 1 (RUNX1), a member of the RUNX family, is one of the key regulatory proteins in vertebrates. RUNX1 is involved in embryonic development, hematopoiesis, angiogenesis, tumorigenesis and immune response. In the past few decades, studies mainly focused on the effect of RUNX1 on acute leukemia and cancer. Only few studies about the function of RUNX1 in the pathological process of pulmonary diseases have been reported. Recent studies have demonstrated that RUNX1 is highly expressed in both mesenchymal and epithelial compartments of the developing and postnatal lung and that it plays a critical role in the lipopolysaccharide induced lung inflammation by regulating the NF-kappa B pathway. RUNX1 participates in the regulation of the NF-.B signaling pathway through interaction with IkB kinase complex in the cytoplasm or interaction with the NF-kappa B subunit P50. NF-kappa B is well-known signaling pathway necessary for inflammatory response in the lung. This review is to highlight the RUNX1 structure, isoforms and to present the mechanism that RUNX1 regulates NF-kappa B. This will illustrate the great potential role of RUNX1 in the inflammation signaling pathway in pulmonary diseases.
引用
收藏
页码:172 / 178
页数:7
相关论文
共 63 条
[1]   Negative regulation of granulocytic differentiation in the myeloid precursor cell line 32Dcl3 by ear-2, a mammalian homolog of Drosophila seven-up, and a chimeric leukemogenic gene, AML1/ETO(MTG8) [J].
Ahn, MY ;
Huang, G ;
Bae, SC ;
Wee, HJ ;
Kim, WY ;
Ito, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1812-1817
[2]   TGF-β-induced repression of CBFA1 by Smad3 decreases cbfa1 and osteocalcin expression and inhibits osteoblast differentiation [J].
Alliston, T ;
Choy, L ;
Ducy, P ;
Karsenty, G ;
Derynck, R .
EMBO JOURNAL, 2001, 20 (09) :2254-2272
[3]   RUNX Genes Find a Niche in Stem Cell Biology [J].
Appleford, Peter J. ;
Woollard, Alison .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 108 (01) :14-21
[4]   CLONING, MAPPING AND EXPRESSION OF PEBP2-ALPHA-C, A 3RD GENE ENCODING THE MAMMALIAN RUNT DOMAIN [J].
BAE, SC ;
TAKAHASHI, E ;
ZHANG, YW ;
OGAWA, E ;
SHIGESADA, K ;
NAMBA, Y ;
SATAKE, M ;
ITO, Y .
GENE, 1995, 159 (02) :245-248
[5]   PEBP2-ALPHA-B/MOUSE AML1 CONSISTS OF MULTIPLE ISOFORMS THAT POSSESS DIFFERENTIAL TRANSACTIVATION POTENTIALS [J].
BAE, SC ;
OGAWA, E ;
MARUYAMA, M ;
OKA, H ;
SATAKE, M ;
SHIGESADA, K ;
JENKINS, NA ;
GILBERT, DJ ;
COPELAND, NG ;
ITO, Y .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :3242-3252
[6]   cDNA cloning of run, a Caenorhabditis elegans Runt domain encoding gene [J].
Bae, SC ;
Lee, J .
GENE, 2000, 241 (02) :255-258
[7]   The RUNX3 gene -: sequence, structure and regulated expression [J].
Bangsow, C ;
Rubins, N ;
Glusman, G ;
Bernstein, Y ;
Negreanu, V ;
Goldenberg, D ;
Lotem, J ;
Ben-Asher, E ;
Lancet, D ;
Levanon, D ;
Groner, Y .
GENE, 2001, 279 (02) :221-232
[8]   AML1 stimulates G1 to S progression via its transactivation domain [J].
Bernardin, F ;
Friedman, AD .
ONCOGENE, 2002, 21 (20) :3247-3252
[9]   The RUNX genes: Gain or loss of function in cancer [J].
Blyth, K ;
Cameron, ER ;
Neil, JC .
NATURE REVIEWS CANCER, 2005, 5 (05) :376-387
[10]  
De Braekeleer E, 2011, FUTURE ONCOL, V7, P77, DOI [10.2217/fon.10.158, 10.2217/FON.10.158]