- Research article
- Open Access
- Open Peer Review
MMP28 (epilysin) as a novel promoter of invasion and metastasis in gastric cancer
© Jian et al; licensee BioMed Central Ltd. 2011
- Received: 13 October 2010
- Accepted: 26 May 2011
- Published: 26 May 2011
The purpose of this study was to investigate invasion and metastasis related genes in gastric cancer.
The transwell migration assay was used to select a highly invasive sub-line from minimally invasive parent gastric cancer cells, and gene expression was compared using a microarray. MMP28 upregulation was confirmed using qRT-PCR. MMP28 immunohistochemistry was performed in normal and gastric cancer specimens. Invasiveness and tumor formation of stable cells overexpressing MMP28 were tested in vitro and in vivo.
MMP28 was overexpressed in the highly invasive sub-cell line. Immunohistochemistry revealed MMP28 expression was markedly increased in gastric carcinoma relative to normal epithelia, and was significantly associated with depth of tumor invasion, lymph node metastasis and poorer overall survival. Ectopic expression of MMP28 indicated MMP28 promoted tumor cell invasion in vitro and increased gastric carcinoma metastasis in vivo.
This study indicates MMP28 is frequently overexpressed during progression of gastric carcinoma, and contributes to tumor cell invasion and metastasis. MMP28 may be a novel therapeutic target for prevention and treatment of metastases in gastric cancer.
- Gastric Cancer
- Gastric Carcinoma
- Gastric Cancer Cell
- Oral Squamous Cell Carcinoma
- MMP28 Expression
Gastric cancer is second only to lung cancer as the leading cause of cancer-related deaths worldwide . Whereas the overall incidence of gastric cancer has declined, the incidence remains high in Asian countries [1, 2]. Although the early stages of gastric cancer are curable, most patients are diagnosed with late-stage disease, which currently has limited successful therapeutic strategies . Surgery and combination chemotherapies confer only modest survival benefits in advanced gastric cancer, resulting in an overall 5 year survival rate of <24% [4, 5]. Therefore, understanding of the molecular and genetic factors involved in gastric cancer progression may identify novel gastric biomarkers and highlight potential avenues of investigation for targeted therapies.
Matrix metalloproteinase 28 (MMP28), also known as epilysin, is a metalloproteinase cloned originally from human keratinocytes, testis, and lung cDNA libraries . In rodents, MMP28 is expressed in many normal adult tissues, including testis, intestine, skin, and lung, suggesting a role in tissue homeostasis . Fetal expression is observed in the brain, kidney and skeletal muscle . Similarly to other MMPs, MMP28 is overexpressed in multiple disease states . In some tumors and cancer cell lines MMP28 expression is increased [9–11]; although in some cases MMP28 protein is downregulated in cancer compared to normal tissues . In wounded skin, strong upregulation of MMP28 occurs in mitotic cells behind the advancing wound edge, but not in actively migrating keratinocytes which secrete other MMPs such as collagenase, stromelysin, and gelatinase . Tumor necrosis factor α (TNFα), but not the ten other growth factors tested, strongly stimulated MMP28 expression in primary cultures of human keratinocytes . A conserved region upstream of the MMP28 transcription initiation site contains a putative NFκB binding site. MMPs act not only as metalloproteinases, as the ability of MMPs to regulate cell behavior is becoming increasingly evident . For example, overexpression of MMP28 in lung adenocarcinoma cells induces an epithelial-to-mesenchymal transition (EMT) via activation of latent TGFβ [14, 15]. MMP28-induced EMT is associated with loss of E-cadherin, a major mediator of cell-cell adhesion, as well as increased expression of MMP-9 (gelatinase B) and MMP-14 (MT1-MMP). The expression of MMP28 is increased in oral squamous cell carcinoma (OSCC) compared to premalignant lesions . Knockdown of MMP28 leads to inhibition of anchorage independent growth in both OSCC (oral squamous cell carcinomas)and esophageal carcinomas.
The results of this study demonstrate MMP28 is overexpressed in a highly invasive sub-line of PAMC82 cells. Immunohistochemical analysis revealed MMP28 is overexpressed in gastric carcinoma relative to normal epithelial cells, and MMP28 is significantly associated with depth of tumor invasion, lymph node metastasis and a poorer overall survival. Our data demonstrates MMP28 is frequently overexpressed during gastric carcinoma progression and contributes to tumor cell invasion and metastasis.
Cell lines and cell culture
Human gastric cancer cell lines PAMC82 , N87, BGC823, SNU16, SNU5, SGC7901, MGC803, AGS and MKN45 were maintained in RPMI 1640 (HyClone, Logan, UT, USA) supplemented with 10% fetal bovine serum (Invitrogen, Carlsbad, CA, USA). To select for a highly invasive subpopulation, PAMC82 cells were seeded on matrigel (BD Biosciences, Bedford, MA, USA) in 8 μm pore transwell inserts (Costar, Cambridge, MA, USA). Cells which invaded through the membrane and attached to the lower well were harvested and expanded. Serial selection of cells for increased invasiveness was continued for three generations, and the sub-lines from the three different generations were designated as PAMC82-P1, PAMC82-P2 and PAMC82-P3 respectively.
A 22K Human Genome Array, a product of the Human Genome Oligo Set Version 2.1 (http://www.Operon.com) was used to compare gene expression profiles in PAMC82-P3 relative to PAMC82 at the Bioassay Laboratory, CapitalBio Corporation Beijing, China. Data on the gene array is provided in supplementary data S1.
Total cellular RNA preparation and reverse transcription of 4 μg total cellular RNA to cDNA was performed as previously described [18, 19], and cDNA was diluted 1:10 and used for PCR. Using the published cDNA sequence (GenBank Accession no. AF219624) primers were designed to amplify a 258-bp product of human MMP-28 (forward: 5'-CTCATCCTCTTCAAGGGTG-3', nt 1,366 to 1,383 and reverse: 5'-GGAAGAAGATGATGGAGCCA-3', nt 1,606 to 1,623). The U6 gene was used as an endogenous control (forward 5'-GCTTCGGCAGCACATATACTAAAAT-3' and reverse 5'-CGCTTCACGAATTTGCGTGTCAT-3') amplifying a 89 bp product. Primers and probes were obtained from Applied Biosystems (Carlsbad, CA, USA) and qRT-PCR was performed as previously described .
Immunohistochemical staining of gastric carcinoma tissue
MMP28 expression was determined by immunohistochemistry in 304 clinical cases of gastric cancer, of which clinical follow-up data was available for 274 patients. In addition, 30 of these specimens had paired normal gastric epithelia and another 30 had paired lymph node metastasis. Immunostaining was performed using the CSA kit (DAKO, Glostrup, Denmark) with a 1 h incubation of an anti-MMP28 antibody (M5066, 2 μg/ml, Sigma, St. Louis, MO, USA) in citrate buffer. Slides were evaluated by two pathologists and MMP28 expression was semi-quantitatively scored based on the staining intensity and percentage of cells stained. Tissues with no staining were scored as 0, faint staining, moderate or strong staining in <25% of cells scored as 1, moderate staining or strong staining in 25-50% cells scored as 2 and strong staining in >50% cells was scored 3.
MMP28 overexpressing N87 cells
PCR primers incorporating BamHI (5') and XhoI (3') (restriction sites underlined; forward 5'-CGCGGATCCGCCGCCGCCATGGTCGCGCGCGTCGGCCTC-3' and reverse 5'-ACGTCTCGAGCCGAACAGGGCGCTCCCCGAGTTG-3') were designed to amplify and clone human MMP28 into the pcDNA3.1 expression vector (Invitrogen) containing a C-terminus His-6 epitope to produce the pcDNA3.1-MMP28-c-His vector. Sequencing of the cloned gene was performed in both directions. The pcDNA3.1-MMP28-c-His vector was transfected into the gastric cancer cell line N87 and stable cell lines were selected by incubation with 500 μg/ml G418 for 2 weeks.
Western blot analysis
Proteins were separated by sodium dodecylsulphate-polyacrylamide gel (SDS-PAGE) electrophoresis, transferred to polyvinylidene difluoride membranes (PVDF; Millipore, Bedford, MA, USA), blocked and then probed with anti-MMP28 (0.2 μg/ml, M5066, Sigma, St. Louis, MO, USA) and ß-actin (1:5,000, Sigma) antibodies. After washing, the blots were incubated with horseradish peroxidase-conjugated secondary antibodies and visualized using an enhanced chemiluminescence kit (Pierce, Rockford, IL, USA).
Matrigel chemoinvasion assay
The matrigel chemoinvasion assay was performed as previously described, with some modifications. Briefly, 4 × 104 cells were seeded onto 6.5 mm Costar transwells (Corning, Lowell, MA, USA) coated with 150 μg/ml matrigel. After incubation for 24 h at 37°C, cells which remained inside the insert were removed with a cotton swab and cells which had invaded to the lower surface of the membrane were fixed in 50:50 methanol: acetone and stained with 4,6-diamidino-2-phenylindole (DAPI). After air drying the membrane, the number of cells in three random x100 fields was counted using a fluorescence microscope. Experiments were performed in triplicate and repeated twice; therefore, the values represent the mean number of invasive cells in 18 × 100 fields of view. Differences in value distribution were analyzed using one-way ANOVA, p < 0.05 was considered significant.
Xenograft assays in nude mice
Nu/nu mice were obtained from the Jackson Laboratory (Vital River, Beijing, China) and maintained in a specific pathogen-free facility at the Experimental Center of the Chinese Academy of Medical Science, which is accredited by the Chinese Association for Accreditation of Laboratory Animal Care. For the spontaneous metastasis assay, stable MMP28 over-expressing N87 cells (N87-C9 and N87-C10) or control cells (N87-Ve) were subcutaneously injected into female 4-wk-old mice. The mice were euthanized 9 weeks after injection and examined for subcutaneous tumor growth and development of metastases.
Invasion assay results were compared using One-way ANOVA. Statistical analyses of MMP28 expression and clinicopathological data was performed using Fisher's exact test. For survival analysis, Kaplan-Meier survival curves were constructed and tested by the log-rank test, p < 0.05 were considered statistically significant.
MMP28 is overexpressed in the highly invasive PAMC82-P3 sub-line
MMP28 is overexpressed in gastric carcinoma and correlates with poorer survival
Association of MMP28 protein expression with clinico-pathological characteristics in 274 primary gastric tumors
MMP28 expression score
pT (primary tumor)
pN (lymph node metastasis)
pM (distant metastasis)
Cox multivariate analysis of MMP28 expression and clinico-pathological features in gastric cancer.
Risk ratio (95% CI)
pT (primary tumor)
pN (lymph node metastasis)
pM (distant metastasis)
Score of MMP28 expression
MMP28 overexpression increases the invasive ability of gastric cancer cells
MMP28 promotes growth and spontaneous metastasis of gastric cancers in vivo
To define the function of MMP28 in vivo, we subcutaneously injected MMP28-overexpressing N87 clones (N87-C9 and C10) into athymic mice, and mice were euthanized 9 weeks later. MMP28 significantly promoted growth of N87 xenografts (MMP28-C9: 4.32 ± 2.45 cm3; MMP28-C10: 4.45 ± 1.38 cm3) compared to transfected control (N87-Pa: 2.87 ± 1.45 cm3) or control N87 cells (N87-Ve: 2.99 ± 1.24 cm3, p < 0.05 Figure 3C). Expression of MMP28 increased volume and weight of tumors, so the proliferation rate of the MMP-28 overexpressing clones C9 and C10 was analyzed, and found to be not significantly different to control cells (data not shown). Ki67 expression in all xenograft tumors groups was similar (Figure 3D). As MMP28 increased invasion and tumor volume in the absence of altered proliferation, we hypothesize MMP28 may influence expression of other genes related to tumor growth or vascular formation. MMP28 over expressing N87 (N87-MMP28) xenograft tumors showed a highly invasive pattern in HE staining sections (Figure 3D), indicating MMP28 expression significantly promotes xenograft tumor invasion into the surrounding tissue. MMP28 overexpression also significantly promoted the spontaneous metastasis of N87 cells to lung. The lungs of mice in the N87-MMP28 group had evident metastatic nodules, whereas these were barely visible on the lung surface of the control cohort (Figure 3D). H&E staining revealed a significant increase in lung metastases in MMP overexpressing N87 injected mice (MMP28-C9: 14.3 ± 3.43 and MMP28-C10: 15.6 ± 4.34) compared to mice injected with control cells (N87-Pa: 3.0 ± 0.64 and N87-Ve: 2.0 ± 0.43, p < 0.01 Figure 3D,E).
Metastasis is a multifactorial process, requiring escape of the normal microenvironment by tumor cells, entrance in and out of lymphatic or blood vessels and proliferation in distant tissue microenvironments . Implicit in these stages of metastasis is the critical ability of tumor cells to invade . During invasion, malignant cells reside within two major types of extracellular matrix: the basement membrane or the stromal matrix . Basement membrane is one of the most important barriers against cancer cell invasion . Therefore, for this study, we used BD Matrigel, a solubilized basement membrane preparation, isolated from the Engelbreth-Holm-Swarm mouse sarcoma, to model mimic gastric carcinoma invasion in vivo. Using a transwell chamber, we isolated the highly invasive subpopulation PAMC82-P3 from the parental PAMC82 cell line. In vitro selection provides a useful approach to isolate cell sub-lines with different invasion and metastatic potentials. Microarray analysis was used to determine the genes which may be involved in invasion, and MMP28 was one of the most interesting genes shown to be differentially regulated in PAMC82-P3 cells compared to PAMC cells.
MMP28 (epilysin), structurally belongs to the MMP19 subfamily, and represents one of the newest MMP member. MMP28 is expressed in normal and carcinoma tissues , basal keratinocytes at and surrounding wound edges , in fetal tissues and rhesus monkey placenta during early pregnancy , suggesting a role for MMP28 in normal tissue homeostasis, wound repair, and development, as well as in tumor progression [11, 14]. MMP28 may also be involved in immune function, as it is expressed in normal circulating human T lymphocytes and is upregulated in osteoarthritic cartilage . Few studies have investigated expression of MMP28 in human tumor samples; however, it is overexpressed in oral squamous cell carcinoma . This study demonstrates MMP28 protein is overexpressed in gastric tumors (30/30, 100%) compared to normal epithelia (16/30, 53.3%, p < 0.001). MMP28 protein was expressed in gastric cancer cells and lymph node metastasis and not located in the surrounding normal tissues. This study also indicates MMP28 expression is significantly positively correlated with tumor invasion, lymph node metastasis and tumor-node-metastasis stage (p < 0.001), suggesting MMP28 plays a role in gastric carcinoma invasion and metastasis. Taken together, these data indicate MMP28 plays an important role in gastric cancer progression.
Illman SA et al. demonstrated expression of MMP28 altered cell phenotype towards a more adhesive, less migratory behavior . However, biological evidence from in vitro and in vivo experiments has not yet clarified the relationship between MMP28 and cancer metastasis. In the current study we have shown, to our knowledge for the first time, that MMP28 positively regulates invasion of gastric cancer cells in vitro and can induce a metastatic phenotype in vivo. Increased expression of MMP28 led to a dose-dependent increase in invasive ability of N87 cells. These results provide the first evidence that MMP28 plays an important role in tumor invasion and metastasis and suggest MMP28 may be an effective target for suppression of metastasis in gastric cancer.
We have established a gastric carcinoma invasion model using a highly invasive sub-line of tumor cells in which MMP28 was overexpressed. Further investigation revealed MMP28 is significantly correlated with invasive and metastatic ability and is a valuable marker of poor prognosis in gastric cancer. This study provides the first evidence that MMP28 can promote invasion and metastasis in gastric cancer.
This work was supported by grants from the National Key Basic Research Program (NKBRP; 973 Program, No. 2010CB933902) and the National Natural Science Foundation (30570818 and 30600279).
We thank Professor Zhihua Yang (Cancer Institute/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China) for kindly help.
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