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PubMed:15049011 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 1810-1815 gene:4313 denotes MMP-2
T1 1851-1863 disease:C0029463 denotes osteosarcoma
T2 1810-1815 gene:4313 denotes MMP-2
T3 1851-1863 disease:C0585442 denotes osteosarcoma
R1 T0 T1 associated_with MMP-2,osteosarcoma
R2 T2 T3 associated_with MMP-2,osteosarcoma

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15049011-0#40#45#gene4313 699-783 gene4313 denotes MMP secretion. We, therefore, tested the effect of BPs on tumor cell invasion, MMP-2
15049011-0#65#77#diseaseC0029463 1068-1363 diseaseC0029463 denotes ore and after alendronate treatment. Real-time quantitative RT-PCR was used to determine the mRNA level of MMP-2 with and without alendronate treatment. Enzyme-linked immunosorbent assay (ELISA) was used to quantify the cytokine level of MMP-2 secreted in the condition medium. BP-induced cell a
15049011-0#65#77#diseaseC0585442 1068-1363 diseaseC0585442 denotes ore and after alendronate treatment. Real-time quantitative RT-PCR was used to determine the mRNA level of MMP-2 with and without alendronate treatment. Enzyme-linked immunosorbent assay (ELISA) was used to quantify the cytokine level of MMP-2 secreted in the condition medium. BP-induced cell a
40#45#gene431365#77#diseaseC0029463 15049011-0#40#45#gene4313 15049011-0#65#77#diseaseC0029463 associated_with "MMP secretion. We, therefore, tested the effect of BPs on tumor cell invasion, MMP-2",ore and after alendronate treatment. Real-time quantitative RT-PCR was used to determine the mRNA level of MMP-2 with and without alendronate treatment. Enzyme-linked immunosorbent assay (ELISA) was used to quantify the cytokine level of MMP-2 secreted in the condition medium. BP-induced cell a
40#45#gene431365#77#diseaseC0585442 15049011-0#40#45#gene4313 15049011-0#65#77#diseaseC0585442 associated_with "MMP secretion. We, therefore, tested the effect of BPs on tumor cell invasion, MMP-2",ore and after alendronate treatment. Real-time quantitative RT-PCR was used to determine the mRNA level of MMP-2 with and without alendronate treatment. Enzyme-linked immunosorbent assay (ELISA) was used to quantify the cytokine level of MMP-2 secreted in the condition medium. BP-induced cell a

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 102-836 BACKGROUND denotes Osteosarcoma is the most common malignant bone tumor of childhood. Significant proportions of these patients eventually develop pulmonary metastases and succumb to their disease even after conventional multi-agent chemotherapy and surgical excision. Matrix metalloproteinase (MMP)-2 induced degradation of blood vessel basement membranes is an important pre-requisite for tumor invasion and metastasis. Bisphosphonates (BPs) have been known to inhibit tumor growth and metastasis in some tumors such as breast cancer, renal cell carcinoma, and prostate cancer, and may do so through inhibition of MMP secretion. We, therefore, tested the effect of BPs on tumor cell invasion, MMP-2 secretion, and apoptosis of osteosarcoma cell lines.
T2 848-1426 METHODS denotes Two osteosarcoma cell lines (SaOS-2, U(2)OS) were treated with alendronate (50, 100, and 150 microM) for 24 and 48 hr. Matrigel invasion assay was used to investigate the invasive potential of osteosarcoma cell lines before and after alendronate treatment. Real-time quantitative RT-PCR was used to determine the mRNA level of MMP-2 with and without alendronate treatment. Enzyme-linked immunosorbent assay (ELISA) was used to quantify the cytokine level of MMP-2 secreted in the condition medium. BP-induced cell apoptosis was evaluated by fluorescent flow cytometric analysis.
T3 1452-1955 CONCLUSIONS denotes The results showed that alendronate inhibited cell invasion of both osteosarcoma cell lines in a dose-dependent manner. Alendronate reduced the mRNA level and cellular level of MMP-2 in both cell lines in a time and dose-dependent manner. Alendronate also induced significant apoptosis in both cell lines. Our finding suggests that alendronate downregulates MMP-2 secretion and induces apoptosis in osteosarcoma cells, which may both contribute to the reduction of invasive potential of the tumor cells.