Reversion-inducing cysteine-rich protein with Kazal motif (RECK) expression: an independent prognostic marker of survival in colorectal cancer

被引:14
作者
Stenzinger, Albrecht [2 ,3 ]
von Winterfeld, Moritz [1 ]
Rabien, Anja [4 ]
Warth, Arne [2 ,3 ]
Kamphues, Carsten [5 ]
Dietel, Manfred [1 ]
Weichert, Wilko [2 ,3 ]
Klauschen, Frederick [1 ]
Wittschieber, Daniel [6 ]
机构
[1] Charite Univ Med Berlin, Inst Pathol, D-10117 Berlin, Germany
[2] Heidelberg Univ, Inst Pathol, D-69120 Heidelberg, Germany
[3] Natl Ctr Tumor Dis, D-69120 Heidelberg, Germany
[4] Charite Univ Med Berlin, Dept Urol, D-10117 Berlin, Germany
[5] Charite Univ Med Berlin, Dept Gen Visceral & Transplantat Surg, D-13533 Berlin, Germany
[6] Univ Hosp Munster, Inst Legal Med, D-48149 Munster, Germany
关键词
RECK; Colorectal cancer; Matrix metalloproteinase; MATRIX METALLOPROTEINASES; DECREASED RECK; CARCINOMA; REGULATOR; INVASION; EMMPRIN; MMP-9;
D O I
10.1016/j.humpath.2011.10.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Patient prognosis in colorectal cancer is determined as in most solid cancers by the extent of local invasion and the presence of lymph node and distant metastases. The invasive potential of a tumor depends on the ability to degrade extracellular matrix proteins, for example, by matrix metalloproteinases. An important inhibitor of matrix metalloproteinases is reversion-inducing cysteine-rich protein with Kazal motifs (RECK), a membrane-anchored glycoprotein. This study investigated the prognostic relevance of RECK expression in colorectal cancer in a cohort of 283 patients. Analysis of immunohistochemical tissue microarray data showed that RECK protein levels did not seem to correlate with clinicopathologic parameters (Spearman rank correlation coefficients between -0.14 and -0.18) and that decreased RECK expression was an independent prognostic factor of poor survival, with a mean survival of 70 months in RECK-negative (146 cases) versus 97 months in RECK-positive patients (137 cases) (log-rank test, P = .002). (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1314 / 1321
页数:8
相关论文
共 40 条
  • [1] [Anonymous], PATHOLOG RES INT
  • [2] Epigenetic inactivation of the metastasis suppressor RECK enhances invasion of human colon cancer cells
    Cho, Chun-Yu
    Wang, Jui-Ho
    Chang, Hui-Chiu
    Chang, Chong-Keng
    Hung, Wen-Chun
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 213 (01) : 65 - 69
  • [3] The adenoma-carcinoma sequence and prospects for the prevention of colorectal neoplasia
    Cotton, S
    Sharp, L
    Little, J
    [J]. CRITICAL REVIEWS IN ONCOGENESIS, 1996, 7 (5-6): : 293 - 342
  • [4] Matrix metalloproteinases and the development of cancer
    Coussens, LM
    Werb, Z
    [J]. CHEMISTRY & BIOLOGY, 1996, 3 (11): : 895 - 904
  • [5] A Review of the Most Promising Biomarkers in Colorectal Cancer: One Step Closer to Targeted Therapy
    Deschoolmeester, Vanessa
    Baay, Marc
    Specenier, Pol
    Lardon, Filip
    Vermorken, Jan B.
    [J]. ONCOLOGIST, 2010, 15 (07) : 699 - 731
  • [6] New functions for the matrix metalloproteinases in cancer progression
    Egeblad, M
    Werb, Z
    [J]. NATURE REVIEWS CANCER, 2002, 2 (03) : 161 - 174
  • [7] RECK gene expression in hepatocellular carcinoma: Correlation with invasion-related clinicopathological factors and its clinical significance
    Furumoto, K
    Arii, S
    Mori, A
    Furuyama, H
    Rivas, MJG
    Nakao, T
    Isobe, N
    Murata, T
    Takahashi, C
    Noda, M
    Imamura, M
    [J]. HEPATOLOGY, 2001, 33 (01) : 189 - 195
  • [8] Roles of matrix metalloproteinases in cancer progression and their pharmacological targeting
    Gialeli, Chrisostomi
    Theocharis, Achilleas D.
    Karamanos, Nikos K.
    [J]. FEBS JOURNAL, 2011, 278 (01) : 16 - 27
  • [9] Haggar Fatima A, 2009, Clin Colon Rectal Surg, V22, P191, DOI 10.1055/s-0029-1242458
  • [10] Annual report to the nation on the status of cancer, 1975-2001, with a special feature regarding survival
    Jemal, A
    Clegg, LX
    Ward, E
    Ries, LAG
    Wu, XC
    Jamison, PM
    Wingo, PA
    Howe, HL
    Anderson, RN
    Edwards, BK
    [J]. CANCER, 2004, 101 (01) : 3 - 27