Mortalin is a prognostic factor of gastric cancer with normal p53 function

被引:61
作者
Ando, Koji [1 ]
Oki, Eiji [1 ]
Zhao, Yan [1 ]
Ikawa-Yoshida, Ayae [1 ]
Kitao, Hiroyuki [2 ]
Saeki, Hiroshi [1 ]
Kimura, Yasue [1 ]
Ida, Satoshi [1 ]
Morita, Masaru [1 ]
Kusumoto, Tetsuya [1 ]
Maehara, Yoshihiko [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Sci, Higashi Ku, Fukuoka 8218582, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Mol Oncol, Higashi Ku, Fukuoka 8218582, Japan
关键词
Mortalin; p53; Prognostic factor; TUMOR-SUPPRESSOR P53; HSP70; FAMILY-MEMBER; COLORECTAL-CANCER; PROTEIN; CELLS; MOT-2; OVEREXPRESSION; ACCUMULATION; IDENTIFICATION; SENESCENCE;
D O I
10.1007/s10120-013-0279-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Mortalin is a heat-non-inducible member of the heat shock protein 70 family. Mortalin binds to p53 and prevents p53 from entering the nucleus. To understand the significance of mortalin in gastric cancer, we investigated the expression of mortalin and p53. Expression of mortalin and p53 was examined by immunohistochemical staining of 182 clinical samples of gastric cancer. Mortalin-positive and aberrant p53-positive tumors were found in 75.2 and 49.5 % of cases, respectively. Mortalin-positive tumors were deeper in invasion and had more lymph node and liver metastases compared with mortalin-negative tumors (P < 0.01, P < 0.05, respectively). Mortalin-positive tumors had worse prognosis compared with mortalin-negative tumors (P = 0.035). Moreover, in tumors with normal p53 function, mortalin-positive tumors had worse prognosis compared with mortalin-negative tumors (P = 0.017). Mortalin has a great impact on gastric cancer with normal p53. Therefore, mortalin is a target molecule for treatment of gastric cancer, as well as a promising prognostic factor, especially in tumors with normal p53.
引用
收藏
页码:255 / 262
页数:8
相关论文
共 33 条
[1]
Aikou T, 2001, Nihon Rinsho, V59 Suppl 4, P159
[2]
The UMD-p53 database:: New mutations and analysis tools [J].
Béroud, C ;
Soussi, T .
HUMAN MUTATION, 2003, 21 (03) :176-181
[3]
Mortalin sensitizes human cancer cells to MKT-077-induced senescence [J].
Deocaris, Custer C. ;
Widodo, Nashi ;
Shrestha, Bhupal G. ;
Kaur, Kamaljit ;
Ohtaka, Manami ;
Yamasaki, Kazuhiko ;
Kaul, Sunil C. ;
Wadhwa, Renu .
CANCER LETTERS, 2007, 252 (02) :259-269
[4]
Mortalin is over-expressed by colorectal adenocarcinomas and correlates with poor survival [J].
Dundas, SR ;
Lawrie, LC ;
Rooney, PH ;
Murray, GI .
JOURNAL OF PATHOLOGY, 2005, 205 (01) :74-81
[5]
DEFINITION OF A CONSENSUS BINDING-SITE FOR P53 [J].
ELDEIRY, WS ;
KERN, SE ;
PIETENPOL, JA ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE GENETICS, 1992, 1 (01) :45-49
[6]
ELLEDGE RM, 1994, CANCER RES, V54, P3752
[7]
Hussain SP, 1998, CANCER RES, V58, P4023
[8]
Kaserer K, 2000, J PATHOL, V190, P450
[9]
Structurally and functionally distinct mouse hsp70 family members Mot-1 and Mot-2 proteins are encoded by two alleles [J].
Kaul, SC ;
Duncan, E ;
Sugihara, T ;
Reddel, RR ;
Mitsui, Y ;
Wadhwa, R .
DNA RESEARCH, 2000, 7 (03) :229-231
[10]
Malignant transformation of NIH3T3 cells by overexpression of mot-2 protein [J].
Kaul, SC ;
Duncan, EL ;
Englezou, A ;
Takano, S ;
Reddel, RR ;
Mitsui, Y ;
Wadhwa, R .
ONCOGENE, 1998, 17 (07) :907-911