期刊
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
卷 31, 期 5, 页码 1234-1242出版社
SPANDIDOS PUBL LTD
DOI: 10.3892/ijmm.2013.1292
关键词
breast cancer; invasion; migration; endoplasmic reticulum stress; chemotherapeutic reagents; heparanase
资金
- National Natural Science Foundation of China [81000992, 81072207]
- Natural Science Foundation of Anhui Province [090413135]
- Key Project of the Natural Science Foundation of the Department of Education, Anhui Province, China [KJ2012A202]
Tumor metastasis is the ultimate stage of cancer, and the primary cause of mortality in patients. Tumor cells breaking through the natural barrier consisting of the basement membrane (BM) and extracellular matrix (ECM) is the a crucial step in tumor invasion and metastasis. Thus, protecting this barrier is the key to reducing mortality. Heparanase is a mammalian endo-P-glucuronidase which has been found to promote the cleavage of heparan sulfate (HS), and plays a significant role in tumor cell invasion and metastasis. Although chemotherapeutic reagents have a strong antitumor activity, they may promote the invasion and migration of cancer cells, as has been observed during clinical treatment. Chemotherapeutic reagents can induce endoplasmic reticulum (ER) stress; in this study, we used adriamycin (ADM) and a classical ER stress inducer, tunicamycin (TM). We report that the activation of ER stress is involved in the enhanced invasion and migration ability of breast cancer cells and we hypothesized that this effect is associated with the activation of heparanase. In support of this, we used the heparanase inhibitor, OGT2115, and low molecular weight heparin (LMWH) to inhibit the expression and activity of heparanase, and we found that the invasion and migration ability of the cells was suppressed. Our findings demonstrate that heparanase inhibitors suppress breast cancer cell invasion and migration induced by ER stress, and provide a strong rationale for the development of heparanase-based therapeutics for the prevention of metastasis induced by chemotherapeutic reagents.
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