Combined expression of p53, cyclin D1 and epidermal growth factor receptor improves estimation of prognosis in curatively resected oral cancer

被引:45
作者
Shiraki, M
Odajima, T
Ikeda, T
Sasaki, A
Satoh, M
Yamaguchi, A
Noguchi, M
Nagai, I
Hiratsuka, H
机构
[1] Sapporo Med Univ Hosp, Dept Pathol, Chuo Ku, Sapporo, Hokkaido 0600061, Japan
[2] Sapporo Med Univ, Sch Med, Dept Oral Surg, Sapporo, Hokkaido, Japan
关键词
oral cancer; p53; cyclin D1; EGFR; coexpression; prognosis;
D O I
10.1038/modpathol.3800455
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
p53, cyclin D1 and epidermal growth factor receptor ( EGFR) are molecular markers that regulate the cell cycle or cell growth and play important roles in tumor development and progression. In this study, we examined the impact of immunohistochemical expression of these markers on tumor progression in 140 oral cancers. p53, cyclin D1 and EGFR were expressed in 64 cases ( 46%), 54 cases ( 39%) and 54 cases ( 39%), respectively, but there was no inter-relationship between any two of these markers. In the association of these markers with clinicopathological features, EGFR expression alone was significantly associated with poor differentiation ( P = 0.0008) and invasive growth pattern ( P = 0.0003). Any of these markers, including EGFR, had no significant impact on survival. Coexpression of all these markers, however, was significantly associated with invasive growth pattern ( P = 0.0149) and shortened survival ( P = 0.0181), and was a significant and independent unfavorable prognostic factor ( P = 0.0002), along with tumor size ( P = 0.0040), nodal metastasis ( P = 0.0137) and growth pattern ( P = 0.0017) in a multivariate analysis. Simultaneous coexpression of these markers in oral cancers might prove to be a useful indicator for identification of low-or high-risk patients.
引用
收藏
页码:1482 / 1489
页数:8
相关论文
共 51 条
  • [1] Ang KK, 2002, CANCER RES, V62, P7350
  • [2] The expression of cyclins D1 and E in predicting short-term survival in squamous cell carcinoma of the lung
    Anton, RC
    Coffey, DM
    Gondo, MM
    Stephenson, MA
    Brown, RW
    Cagle, PT
    [J]. MODERN PATHOLOGY, 2000, 13 (11) : 1167 - 1172
  • [3] Co-localization of multiple ErbB receptors in stratified epithelium of oral squamous cell carcinoma
    Bei, R
    Pompa, G
    Vitolo, D
    Moriconi, E
    Ciocci, L
    Quaranta, M
    Frati, L
    Kraus, MH
    Muraro, R
    [J]. JOURNAL OF PATHOLOGY, 2001, 195 (03) : 343 - 348
  • [4] Bova RJ, 1999, CLIN CANCER RES, V5, P2810
  • [5] DelSal G, 1996, ONCOGENE, V12, P177
  • [6] THE SUBCELLULAR-LOCALIZATION OF THE NEU PROTEIN IN HUMAN NORMAL AND NEOPLASTIC-CELLS
    DEPOTTER, CR
    QUATACKER, J
    MAERTENS, G
    VANDAELE, S
    PAUWELS, C
    VERHOFSTEDE, C
    EECHAUTE, W
    ROELS, H
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1989, 44 (06) : 969 - 974
  • [7] ACTIVATING MUTATIONS FOR TRANSFORMATION BY P53 PRODUCE A GENE-PRODUCT THAT FORMS AN HSC70-P53 COMPLEX WITH AN ALTERED HALF-LIFE
    FINLAY, CA
    HINDS, PW
    TAN, TH
    ELIYAHU, D
    OREN, M
    LEVINE, AJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (02) : 531 - 539
  • [8] Fracchiolla NS, 1997, CANCER-AM CANCER SOC, V79, P1114, DOI 10.1002/(SICI)1097-0142(19970315)79:6<1114::AID-CNCR9>3.3.CO
  • [9] 2-I
  • [10] Gansauge S, 1997, CANCER RES, V57, P1634