Inhibition of ovarian cancer cell metastasis by a fusion polypeptide Tat-ELP
Autor: | Michael F. Flessner, Abby Tausend, Drazen Raucher, Iqbal Massodi, Aisha Davis, Kimberly Credit, Gene L. Bidwell |
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Rok vydání: | 2009 |
Předmět: |
Cancer Research
Recombinant Fusion Proteins Transplantation Heterologous Cell Mice Nude Biology Metastasis Extracellular matrix Mice Cell Movement Cell Adhesion medicine Animals Humans Neoplasm Invasiveness Neoplasm Metastasis Cell adhesion Receptor Ovarian Neoplasms Mice Inbred BALB C attachment - elastin-like polypeptide (ELP) - metastasis - SKOV-3 - Tat Cancer General Medicine medicine.disease Molecular biology Elastin Cell Adhesion Process medicine.anatomical_structure Oncology Cancer research Female tat Gene Products Human Immunodeficiency Virus Peptides Ovarian cancer Neoplasm Transplantation |
Zdroj: | Clinical & Experimental Metastasis. 26:251-260 |
ISSN: | 1573-7276 0262-0898 |
Popis: | Tumor cell metastasis is a complex, multi-step process that is a major cause of death and morbidity amongst cancer patients. Cell adhesion plays a critical role in the development of metastatic cancer, and it is mediated by interactions between receptors on the cell surface and ligands of the extracellular matrix or other surfaces. Therefore, inhibition of the cell adhesion process appears to be an effective method of preventing metastasis. This work describes a genetically engineered polypeptide with the potential to prevent cell adhesion and inhibit metastasis. We have found that the cell penetrating peptide Tat, fused with elastin-like polypeptide (ELP) inhibited adhesion, spreading, invasion and migration of SKOV-3 ovarian cancer cells in cell culture. Furthermore, we have also confirmed that Tat-ELP has anti-metastatic potential in an experimental ovarian cancer metastasis model in vivo, causing approximately 80% reduction in the tumor burden. Since cell attachment is an important step in tumor cell invasion and metastasis, these results suggest a novel role of Tat-ELP as a therapeutic intervention in cancer metastasis. Electronic supplementary material The online version of this article (doi:10.1007/s10585-009-9237-z) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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