Assessment of SMAD4, p53, and Ki-67 alterations as a predictor of liver metastasis in human colorectal cancer

被引:12
作者
Kawakami, Masayo [1 ,3 ]
Yamaguchi, Tatsuro [1 ]
Takahashi, Keiichi [1 ]
Matsumoto, Hiroshi [1 ]
Yasutome, Michiya [1 ]
Horiguchi, Shinichiro [2 ]
Hayashi, Yukiko [2 ]
Funata, Nobuaki [2 ]
Mori, Takeo [1 ]
机构
[1] Tokyo Metropolitan Komagome Hosp, Dept Surg, Bunkyo Ku, Tokyo 1138677, Japan
[2] Tokyo Metropolitan Komagome Hosp, Dept Pathol, Bunkyo Ku, Tokyo 1138677, Japan
[3] Tokyo Metropolitan Hiroo Gen Hosp, Dept Surg, Tokyo, Japan
关键词
Colorectal cancer; Liver metastasis; SMAD4; Ki-67; NUCLEAR OVEREXPRESSION; PROGNOSTIC-FACTORS; COLON-CANCER; EXPRESSION; CARCINOMA; GENE; PROTEIN; PROLIFERATION; ADENOCARCINOMAS; IDENTIFICATION;
D O I
10.1007/s00595-009-4028-3
中图分类号
R61 [外科手术学];
学科分类号
摘要
The liver is the most common site of metastasis in patients with colorectal cancer (CRC), and this is a determinant of the prognosis. However, no reliable molecular predictors of liver metastasis have yet been identified. Sixty-two surgical specimens of colorectal cancer were studied. The first group included 25 patients who achieved a disease-free survival period of at least 6 years (CRC-M0), and the second group included 37 patients with synchronous (n = 22) or metachronous (n = 15) liver metastasis (CRC-M1). SMAD4, p53, and Ki-67 expression levels were assessed immunohistochemically. The loss of SMAD4 expression and elevated Ki-67 expression were found significantly more frequently in CRC-M1 patients than in CRC-M0 patients (P = 0.0047 and P = 0.013, respectively). Statistically significant differences were also observed between the CRC-M0 group and the metachronous metastasis group. No difference was seen in the overexpression of p53 between the groups. A combination analysis of SMAD4 and Ki-67 revealed no cases with maintained levels of SMAD4 and a low Ki-67 expression had or developed liver metastasis. The loss of SMAD4 expression and elevated Ki-67 expression was therefore found to significantly correlate with liver metastasis, regardless of the time of occurrence, thus indicating these factors to be predictive markers for liver metastasis in patients with CRC.
引用
收藏
页码:245 / 250
页数:6
相关论文
共 34 条
[1]   SMAD4 as a prognostic marker in colorectal cancer [J].
Alazzouzi, H ;
Alhopuro, P ;
Salovaara, R ;
Sammalkorpi, H ;
Järvinen, H ;
Mecklin, JP ;
Hemminki, A ;
Schwartz, S ;
Aaltonen, LA ;
Arango, D .
CLINICAL CANCER RESEARCH, 2005, 11 (07) :2606-2611
[2]   Prognostic value of thymidylate synthase, Ki-67, and p53 in patients with Dukes' B and C colon cancer:: A national cancer institute-national surgical adjuvant breast and bowel project collaborative study [J].
Allegra, CJ ;
Paik, S ;
Colangelo, LH ;
Parr, AL ;
Kirsch, I ;
Kim, G ;
Klein, P ;
Johnston, PG ;
Wolmark, N ;
Wieand, HS .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (02) :241-250
[3]  
Arends JW, 2000, J PATHOL, V190, P412
[4]   EVALUATION OF 6 ANTIBODIES FOR IMMUNOHISTOCHEMISTRY OF MUTANT P53 GENE-PRODUCT IN ARCHIVAL COLORECTAL NEOPLASMS [J].
BAAS, IO ;
MULDER, JWR ;
OFFERHAUS, GJA ;
VOGELSTEIN, B ;
HAMILTON, SR .
JOURNAL OF PATHOLOGY, 1994, 172 (01) :5-12
[5]   p53 and Ki-ras as prognostic factors for Dukes' stage B colorectal cancer [J].
Bouzourene, H ;
Gervaz, P ;
Cerottini, JP ;
Benhattar, J ;
Chaubert, P ;
Saraga, E ;
Pampallona, S ;
Bosman, FT ;
Givel, JC .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (08) :1008-1015
[6]   Ki67 protein: the immaculate deception? [J].
Brown, DC ;
Gatter, KC .
HISTOPATHOLOGY, 2002, 40 (01) :2-11
[7]   Colorectal cancer in the adjuvant setting: perspectives on treatment and the role of prognostic factors [J].
Cascinu, S ;
Georgoulias, V ;
Kerr, D ;
Maughna, T ;
Labianca, R ;
Ychou, M .
ANNALS OF ONCOLOGY, 2003, 14 :25-29
[8]  
Dziegiel P, 2003, HISTOL HISTOPATHOL, V18, P401, DOI 10.14670/HH-18.401
[9]  
*ED BOARD CANC STA, CANC STAT JAP 2007
[10]   MADR2 maps to 18q21 and encodes a TGF beta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma [J].
Eppert, K ;
Scherer, SW ;
Ozcelik, H ;
Pirone, R ;
Hoodless, P ;
Kim, H ;
Tsui, LC ;
Bapat, B ;
Gallinger, S ;
Andrulis, IL ;
Thomsen, GH ;
Wrana, JL ;
Attisano, L .
CELL, 1996, 86 (04) :543-552