Centromere protein H is a novel prognostic marker for nasopharyngeal carcinoma progression and overall patient survival

被引:45
作者
Liao, Wen-Ting
Song, Li-Bing
Zhang, Hui-Zhong
Zhang, Xing
Zhang, Ling
Liu, Wan-Li
Feng, Yan
Guo, Bao-Hong
Mai, Hai-Qiang
Cao, Su-Mei
Li, Man-Zhi
Qin, Hai-De
Zeng, Yi-Xin
Zeng, Mu-Sheng
机构
[1] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol So China, Guangzhou 510060, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Dept Expt Res, Guangzhou 510060, Peoples R China
[3] Sun Yat Sen Univ, Ctr Canc, Dept Nasopharyngeal Carcinoma, Guangzhou 510060, Peoples R China
[4] Sun Yat Sen Univ, Ctr Canc, Dept Pathol, Guangzhou 510060, Peoples R China
关键词
D O I
10.1158/1078-0432.CCR-06-1512
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of the present study was to analyze the expression of Centromere protein H (CENP-H), one of the fundamental components of the human active kinetochore, in nasopharyngeal carcinoma (NPC) and to correlate it with clinicopathologic data, including patient survival, Experimental Design: Using reverse transcription-PCR and Western blot, we detected the expression of CENP-H in normal nasopharyngeal epithelial cells, immortalized nasopharyngeal epithelial cell lines, and NPC cell lines. Using immunohistochemistry, we analyzed CENP-H protein expression in 160 clinicopathologically characterized NPC cases. Statistical analyses were applied to test for prognostic and diagnostic associations. Results: Reverse transcription-PCR and Western blot showed that the expression level of CENP-H was higher in NPC cell lines and in immortalized nasopharyngeal epithelial cells than in the normal nasopharyngeal epithelial cell line at both transcriptional and translational levels. By immunohistochemical analysis, we found that 76 of 160 (47.5%) paraffin-embedded archival NPC biopsies showed high expression of CENP-H. Statistical analysis showed that there was a significant difference of CENP-H expression in patients categorized according to clinical stage (P = 0.024) and T classification (P = 0.027). Patients with higher CENP-H expression had shorter overall survival time, whereas patients with lower CENP-H expression had better survival. A prognostic value of CENP-H was also found of the subgroup of N-0-N-1 tumor classification. Multivariate analysis showed that CENP-H expression was an independent prognostic indicator for patient's survival. Conclusions: Our results suggest that CENP-H protein is a valuable marker of NPC progression. High CENP-H expression is associated with poor overall survival in NPC patients.
引用
收藏
页码:508 / 514
页数:7
相关论文
共 48 条
  • [1] Human INCENP colocalizes with the Aurora-B/AIRK2 kinase on chromosomes and is overexpressed in tumour cells
    Adams, RR
    Eckley, DM
    Vagnarelli, P
    Wheatley, SP
    Gerloff, DL
    Mackay, AM
    Svingen, PA
    Kaufmann, SH
    Earnshaw, WC
    [J]. CHROMOSOMA, 2001, 110 (02) : 65 - 74
  • [2] ASSOCIATION OF P53 PROTEIN EXPRESSION WITH TUMOR-CELL PROLIFERATION RATE AND CLINICAL OUTCOME IN NODE-NEGATIVE BREAST-CANCER
    ALLRED, DC
    CLARK, GM
    ELLEDGE, R
    FUQUA, SAW
    BROWN, RW
    CHAMNESS, GC
    OSBORNE, CK
    MCGUIRE, WL
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (03) : 200 - 206
  • [3] A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers
    Bischoff, JR
    Anderson, L
    Zhu, YF
    Mossie, K
    Ng, L
    Souza, B
    Schryver, B
    Flanagan, P
    Clairvoyant, F
    Ginther, C
    Chan, CSM
    Novotny, M
    Slamon, DJ
    Plowman, GD
    [J]. EMBO JOURNAL, 1998, 17 (11) : 3052 - 3065
  • [4] MIF2 IS REQUIRED FOR MITOTIC SPINDLE INTEGRITY DURING ANAPHASE SPINDLE ELONGATION IN SACCHAROMYCES-CEREVISIAE
    BROWN, MT
    GOETSCH, L
    HARTWELL, LH
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 123 (02) : 387 - 403
  • [5] Mutations of mitotic checkpoint genes in human cancers
    Cahill, DP
    Lengauer, C
    Yu, J
    Riggins, GJ
    Willson, JKV
    Markowitz, SD
    Kinzler, KW
    Vogelstein, B
    [J]. NATURE, 1998, 392 (6673) : 300 - 303
  • [6] AUTOIMMUNITY TO THE CELL CYCLE-DEPENDENT CENTROMERE PROTEIN P330(D)/CENP-F IN DISORDERS ASSOCIATED WITH CELL-PROLIFERATION
    CASIANO, CA
    HUMBEL, RL
    PEEBLES, C
    COVINI, G
    TAN, EM
    [J]. JOURNAL OF AUTOIMMUNITY, 1995, 8 (04) : 575 - 586
  • [7] CASIANO CA, 1993, J CELL SCI, V106, P1045
  • [8] Chen YJ, 1999, GENE CHROMOSOME CANC, V25, P169, DOI 10.1002/(SICI)1098-2264(199906)25:2<169::AID-GCC13>3.3.CO
  • [9] 2-9
  • [10] Clark GM, 1997, CANCER RES, V57, P5505