POU domain transcription factor BRN2 is crucial for expression of ASCL1, ND1 and neuroendocrine marker molecules and cell growth in small cell lung cancer

被引:46
作者
Ishii, Jun [1 ,2 ]
Sato, Hanako [3 ]
sakaeda, Masashi [1 ,2 ]
Shishido-Hara, Yukiko [2 ]
Hiramatsu, Chie [3 ]
Kamma, Hiroshi [2 ]
Shimoyamada, Hiroaki [2 ]
Fujiwara, Masachika [2 ]
Endo, Tetsuya [2 ,4 ]
Aoki, Ichiro [1 ]
Yazawa, Takuya [2 ]
机构
[1] Yokohama City Univ, Grad Sch Med, Dept Pathol, Yokohama, Kanagawa 232, Japan
[2] Kyorin Univ, Sch Med, Dept Pathol, Mitaka, Tokyo 1818611, Japan
[3] St Marianna Univ, Sch Med, Dept Anat, Kawasaki, Kanagawa, Japan
[4] Jichi Med Univ, Dept Gen Thorac Surg, Shimotsuke, Japan
关键词
ASCL1; BRN2; cell growth; NeuroD1; neuroendocrine marker; POU domain transcription factor; small cell lung cancer; FUNCTIONAL-NEURONS; DIRECT CONVERSION; MOUSE MODEL; DIFFERENTIATION; FIBROBLASTS; CARCINOMA; BINDING; GENE; HYPOTHALAMUS; MECHANISMS;
D O I
10.1111/pin.12042
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BRN2 is a developmental neural cell-specific POU domain transcription factor and is crucial for cell lineage determination. We investigated the importance of BRN2 in the expression of the lineage-specific transcription factors (achaete-scute homolog-like 1 (ASCL1) and NeuroD1 (ND1)) and neural/neuroendocrine marker molecules (neural cell adhesion molecule 1 (NCAM1), synaptophysin (SYP) and chromogranin A (CHGA)) in small cell lung cancer (SCLC) using cultured lung cancer cells. All examined SCLC cell lines expressed BRN2, as well as ASCL1, ND1, NCAM1, SYP and CHGA. The expression levels of ASCL1, ND1, NCAM1, SYP and CHGA considerably decreased when BRN2 was knocked down in SCLC cells, and the addition of a BRN2 transgene into non-SCLC (NSCLC) cells induced the expression of ASCL1, ND1, NCAM1, SYP and CHGA. However, the BRN2 gene was not activated by the forced expression of ASCL1 or ND1 in NSCLC cells. The knockdown of BRN2 caused significant growth retardation with decrease of S to G2 phase population and mitotic cell rates and unaltered Ki-67-labeled or apoptotic cell rates in SCLC cells, indicating increase of G1 phase population. These findings suggest that BRN2 is a higher level regulator than ASCL1 and ND1 and BRN2 might be involved in aggressiveness of SCLC.
引用
收藏
页码:158 / 168
页数:11
相关论文
共 48 条
[41]  
Travis William D, 2009, Eur J Cancer, V45 Suppl 1, P251, DOI 10.1016/S0959-8049(09)70040-1
[42]   Direct conversion of fibroblasts to functional neurons by defined factors [J].
Vierbuchen, Thomas ;
Ostermeier, Austin ;
Pang, Zhiping P. ;
Kokubu, Yuko ;
Suedhof, Thomas C. ;
Wernig, Marius .
NATURE, 2010, 463 (7284) :1035-U50
[43]   POU-domain proteins: structure and function developmental regulators [J].
Wegner, Michael ;
Drolet, Daniel W. ;
Rosenfeld, Michael G. .
CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (03) :488-498
[44]   Molecular genetics of small cell lung carcinoma [J].
Wistuba, II ;
Gazdar, AF ;
Minna, JD .
SEMINARS IN ONCOLOGY, 2001, 28 (02) :3-13
[45]   EXPRESSION OF A LARGE FAMILY OF POU-DOMAIN REGULATORY GENES IN MAMMALIAN BRAIN-DEVELOPMENT [J].
XI, H ;
TREACY, MN ;
SIMMONS, DM ;
INGRAHAM, HA ;
SWANSON, LW ;
ROSENFELD, MG .
NATURE, 1989, 340 (6228) :35-42
[46]   One hundred years after "Carcinoid": Epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States [J].
Yao, James C. ;
Hassan, Manal ;
Phan, Alexandria ;
Dagohoy, Cecile ;
Leary, Colleen ;
Mares, Jeannette E. ;
Abdalla, Eddie K. ;
Fleming, Jason B. ;
Vauthey, Jean-Nicolas ;
Rashid, Asif ;
Evans, Douglas B. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (18) :3063-3072
[47]   Complicated mechanisms of class II transactivator transcription deficiency in small cell lung cancer and neuroblastoma [J].
Yazawa, T ;
Ito, T ;
Kamma, H ;
Suzuki, T ;
Okudela, K ;
Hayashi, H ;
Horiguchi, H ;
Ogata, T ;
Mitsui, H ;
Ikeda, M ;
Kitamura, H .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (01) :291-300
[48]   Neuroendocrine Cancer-Specific Up-Regulating Mechanism of Insulin-Like Growth Factor Binding Protein-2 in Small Cell Lung Cancer [J].
Yazawa, Takuya ;
Sato, Hanako ;
Shimoyamada, Hiroaki ;
Okudela, Koji ;
Woo, Tetsukan ;
Tajiri, Michihiko ;
Ogura, Takashi ;
Ogawa, Nobuo ;
Suzuki, Takehisa ;
Mitsui, Hideaki ;
Ishii, Jun ;
Miyata, Chie ;
Sakaeda, Masashi ;
Goto, Kazuya ;
Kashiwagi, Korehito ;
Masuda, Munetaka ;
Takahashi, Takashi ;
Kitamura, Hitoshi .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 175 (03) :976-987