Activation of CDCA1-KNTC2, members of centromere protein complex, involved in pulmonary carcinogenesis

被引:124
作者
Hayama, Satoshi
Daigo, Yataro
Kato, Tatsuya
Ishikawa, Nobuhisa
Yamabuki, Takumi
Miyamoto, Masaki
Ito, Tomoo
Tsuchiya, Eiju
Kondo, Satoshi
Nakamura, Yusuke
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Mol Med,Minato Ku, Tokyo 1088639, Japan
[2] Hokkaido Univ, Grad Sch Med, Dept Surg Oncol, Sapporo, Hokkaido 060, Japan
[3] Hokkaido Univ, Grad Sch Med, Dept Surg Pathol, Sapporo, Hokkaido 060, Japan
[4] Kanagawa Canc Ctr, Res Inst, Kanagawa, Japan
关键词
CELL LUNG-CANCER; AURORA-KINASE INHIBITORS; EXPRESSION PROFILES; CHROMOSOME SEGREGATION; THERAPEUTIC TARGET; ANTICANCER DRUGS; GENE-EXPRESSION; CDNA MICROARRAY; BREAST-CANCER; KINETOCHORE;
D O I
10.1158/0008-5472.CAN-06-2137
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We found cotransactivation of cell division associated 1 (CDCA1) and kinetochore associated 2 (KNTC2), members of the evolutionarily conserved centromere protein complex, in non-small cell lung carcinomas (NSCLC). Immunobistochemical analysis using lung cancer tissue microarray confirmed high levels of CDCA1 and KNTC2 proteins in the great majority of lung cancers of various histologic types. Their elevated expressions were associated with poorer prognosis of NSCLC patients. Knockdown of either CDCA1 or KNTC2 expression with small interfering RNA significantly suppressed growth of NSCLC cells. Furthermore, inhibition of their binding by a cell-permeable peptide carrying the CDCA1-derived 19-amino-acid peptide (11R-CDCA1(398-416)) that correspond to the binding domain to KNTC2 effectively suppressed growth of NSCLC cells. As our data imply that human CDCA1 and KNTC2 seem to fall in the category of cancer-testis antigens, and that their simultaneous up-regulation is a frequent and important feature of cell growth/survival of lung cancer, selective suppression of CDCA1 or KNTC2 activity and/or inhibition of the CDCA1-KNTC2 complex formation could be a promising therapeutic target for treatment of lung cancers.
引用
收藏
页码:10339 / 10348
页数:10
相关论文
共 41 条
[1]   Cell-permeable peptide inhibitors of JNK novel blockers of β-cell death [J].
Bonny, C ;
Oberson, A ;
Negri, S ;
Sauser, C ;
Schorderet, DF .
DIABETES, 2001, 50 (01) :77-82
[2]   Identification and validation of prognostic markers in breast cancer with the complementary use of array-CGH and tissue microarrays [J].
Callagy, G ;
Pharoah, P ;
Chin, SF ;
Sangan, T ;
Daigo, Y ;
Jackson, L ;
Caldas, C .
JOURNAL OF PATHOLOGY, 2005, 205 (03) :388-396
[3]   HEC, a novel nuclear protein rich in leucine heptad repeats specifically involved in mitosis [J].
Chen, YM ;
Riley, DJ ;
Chen, PL ;
Lee, WH .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (10) :6049-6056
[4]   Selective killing of transformed cells by cyclin/cyclin-dependent kinase 2 antagonists [J].
Chen, YNP ;
Sharma, SK ;
Ramsey, TM ;
Jiang, L ;
Martin, MS ;
Baker, K ;
Adams, PD ;
Bair, KW ;
Kaelin, WG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4325-4329
[5]   A simple and reliable pretreatment protocol facilitates fluorescent in situ hybridisation on tissue microarrays of paraffin wax embedded tumour samples [J].
Chin, SF ;
Daigo, Y ;
Huang, HE ;
Iyer, NG ;
Callagy, G ;
Kranjac, T ;
Gonzalez, M ;
Sangan, T ;
Earl, H ;
Caldas, C .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2003, 56 (05) :275-279
[6]   Architecture of the human Ndc80-Hec1 complex, a critical constituent of the outer kinetochore [J].
Ciferri, C ;
De Luca, J ;
Monzani, S ;
Ferrari, KJ ;
Ristic, D ;
Wyman, C ;
Stark, H ;
Kilmartin, J ;
Salmon, ED ;
Musacchio, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (32) :29088-29095
[7]   Nuf2 and Hec1 are required for retention of the checkpoint proteins Mad1 and Mad2 to kinetochores [J].
DeLuca, JG ;
Howell, BJ ;
Canman, JC ;
Hickey, JM ;
Fang, GW ;
Salmon, ED .
CURRENT BIOLOGY, 2003, 13 (23) :2103-2109
[8]   KNL-1 directs assembly of the microtubule-binding interface of the kinetochore in C. elegans [J].
Desai, A ;
Rybina, S ;
Müller-Reichert, T ;
Shevchenko, A ;
Shevchenko, A ;
Hyman, A ;
Oegema, K .
GENES & DEVELOPMENT, 2003, 17 (19) :2421-2435
[9]   Dawn of Aurora kinase inhibitors as anticancer drugs [J].
Doggrell, SA .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2004, 13 (09) :1199-1201
[10]   Depression of MAD2 inhibits apoptosis of gastric cancer cells by upregulating Bcl-2 and interfering mitochondrion pathway [J].
Du, Yulei ;
Yin, Fang ;
Liu, Changj'iang ;
Hu, Shengjuan ;
Wang, Jun ;
Xie, Huahong ;
Hong, Liu ;
Fan, Daiming .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 345 (03) :1092-1098