MMP13 is potentially a new tumor marker for breast cancer diagnosis

被引:71
作者
Chang, Hui-Jen
Yang, Ming-Je [2 ]
Yang, Yu-Hsiang
Hou, Ming-Feng [3 ,4 ]
Hsueh, Er-Jung [5 ,6 ]
Lin, Shiu-Ru [1 ]
机构
[1] Fooyin Univ, Biomed Technol Dev Ctr, Sch Med & Hlth Sci, Kaohsiung Cty 831, Taiwan
[2] Kaohsiung Univ, Grad Inst Med, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Fac Biomed Sci & Environm Biol, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ Hosp, Dept Surg, Div Gastrointestinal & Gen Surg, Kaohsiung, Taiwan
[5] Pingtung Christian Hosp, Dept Internal Med, Pingtung, Taiwan
[6] Pingtung Christian Hosp, Div Oncol & Hematol, Pingtung, Taiwan
关键词
MMP13; tumor marker; breast cancer; COLLAGENASE-3; MMP-13; EXPRESSION; MATRIX METALLOPROTEINASES; COLORECTAL-CANCER; MEMBRANE ARRAY; HEAD; CARCINOGENESIS; BIOINFORMATICS; INVASIVENESS; ASSOCIATION; STATISTICS;
D O I
10.3892/or_00000544
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Within the past decade, the incidence of breast cancer in Taiwan has been rising year after year. Breast cancer is the first most prevalent cancer and the fourth leading cause of cancer-related deaths among women in Taiwan. The early stage of breast cancer not only have a wider range of therapeutic options, but also obtain a higher success rate of therapy than those with advanced breast cancer. A test for tumor markers is the most convenient method to screen for breast cancer. However, the tumor markers currently available for breast cancer detection include carcinoembryonic antigen (CEA), carbohydrate antigen 15.3 (CA15.3), and carbohydrate antigen 27.29 (CA27.29) exhibited certain limitations. Poor sensitivity and specificity greatly limits the diagnostic accuracy of these markers. This study aims to identify potential tumor markers for breast cancer. At first, we analyzed genes expression in infiltrating lobular carcinoma, metaplastic carcinoma, and infiltrating ductal carcinoma of paired specimens (tumor and normal tissue) from breast cancer patients using microarray technology. We selected 371 overexpressed genes in all of the three cell type. In advanced breast cancer tissue, we detected four genes MMP13, CAMP, COL10A1 and FLJ25416 from 25 overexpressed genes which encoded secretion protein more specifically for breast cancer than other genes. After validation with 15 pairs of breast cancer tissue and paired to normal adjacent tissues by membrane array and quantitative RT-PCR, we found MMP13 was 100% overexpressed and confirmed to be a secreted protein by Western blot analysis of the cell culture medium. The expression level of MMP13 was also measured by immunohistochemical staining. We suggest that MMP13 is a highly overexpressed secretion protein in breast cancer tissue. It has potential to be a new tumor marker for breast cancer diagnosis.
引用
收藏
页码:1119 / 1127
页数:9
相关论文
共 49 条
[1]
Targeted inhibition of human collagenase-3 (MMP-13) expression inhibits squamous cell carcinoma growth in vivo [J].
Ala-aho, R ;
Ahonen, M ;
George, SJ ;
Heikkilä, J ;
Grènman, R ;
Kallajoki, M ;
Kähäri, VM .
ONCOGENE, 2004, 23 (30) :5111-5123
[2]
Proteomic analysis to identify breast cancer biomarkers in nipple aspirate fluid [J].
Alexander, H ;
Stegner, AL ;
Wagner-Mann, C ;
Du Bois, GC ;
Alexander, S ;
Sauter, ER .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7500-7510
[3]
[Anonymous], 2010, Culture of animal cells: a manual of basic technique and specialized applications
[4]
Bast RC, 1996, J CLIN ONCOL, V14, P2843
[5]
2000 update of recommendations for the use of tumor markers in breast and colorectal cancer: Clinical practice guidelines of the American Society of Clinical Oncology [J].
Bast, RC ;
Ravdin, P ;
Hayes, DF ;
Bates, S ;
Fritsche, H ;
Jessup, JM ;
Kemeny, N ;
Locker, GY ;
Mennel, RG ;
Somerfield, MR .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1865-1878
[6]
Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[7]
Use of Truquant BR radioimmunoassay for early detection of breast cancer recurrence in patients with stage II and stage III disease [J].
Chan, DW ;
Beveridge, RA ;
Muss, H ;
Fritsche, HA ;
Hortobagyi, G ;
Theriault, R ;
Kiang, D ;
Kennedy, BJ ;
Evelegh, M .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) :2322-2328
[8]
Chang MY, 2007, ONCOL REP, V18, P569
[9]
Combination of multiple mRNA markers (PTTG1, survivin, UbcH10 and TK1) in the diagnosis of Taiwanese patients with breast cancer by membrane array [J].
Chen, Chung-Chi ;
Chang, Tsai-Wang ;
Chen, Fang-Ming ;
Hou, Ming-Feng ;
Hung, Sung-Yu ;
Chong, Inn-Wen ;
Lee, Su-Chen ;
Zhou, Tian-Hong ;
Lin, Shiu-Ru .
ONCOLOGY, 2006, 70 (06) :438-446
[10]
Simultaneous detection of multiple mRNA markers CK19, CEA, c-Met, Her2/neu and hMAM with membrane array, an innovative technique with a great potential for breast cancer diagnosis [J].
Chen, Chung-Chi ;
Hou, Ming-Feng ;
Wang, Jaw-Yuan ;
Chang, Tsai-Wang ;
Lai, Dan-Yu ;
Chen, Yi-Fang ;
Hung, Sung-Yu ;
Lin, Shiu-Ru .
CANCER LETTERS, 2006, 240 (02) :279-288