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Secretory leukoprotease inhibitor inhibits cell growth through apoptotic pathway on ovarian cancer
- Source :
- Oncology reports. 19(5)
- Publication Year :
- 2008
-
Abstract
- In light of the poor prognosis for ovarian cancer, research continues for innovative and efficacious treatment modalities. It is now widely accepted that new approaches for the treatment of ovarian cancers are pivotal in further improving prognosis of this disease. Secretory leukoprotease inhibitor (SLPI) is an 11.7-kDa non-glycosylated, serine protease inhibitor that has a broad inhibitory spectrum against serine protease. SLPI showed potential therapeutic inhibitory effects mediated by tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), TNF-alpha, death receptor (DR)-4, DR-5 and TNF receptor (TNFR)-I expression which lead to an activation of apoptosis pathway through Caspase-2, Caspase-8 and Caspase-9. We examined whether levels of SLPI protein expression correlated with clinicopathological characteristics in 58 ovarian cancer samples, and investigated the role of SLPI and its biological functions. SLPI expression showed a significant correlation between low expression of SLPI and amount of ascites (p=0.021), lymph node metastasis (p=0.011). We propose that SLPI could be considered a therapeutic target for the treatment of ovarian cancer.
- Subjects :
- Cancer Research
Glycosylation
Gene Expression Regulation, Enzymologic
TNF-Related Apoptosis-Inducing Ligand
Cell Line, Tumor
medicine
Humans
Secretory Leukocyte Peptidase Inhibitor
Caspase
Cell Proliferation
Ovarian Neoplasms
Oncogene
biology
Tumor Necrosis Factor-alpha
Cancer
General Medicine
medicine.disease
Molecular medicine
Gene Expression Regulation, Neoplastic
Receptors, TNF-Related Apoptosis-Inducing Ligand
Oncology
Apoptosis
Receptors, Tumor Necrosis Factor, Type I
Caspases
Immunology
biology.protein
Cancer research
Tumor necrosis factor alpha
Female
Ovarian cancer
SLPI
Subjects
Details
- ISSN :
- 1021335X
- Volume :
- 19
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Oncology reports
- Accession number :
- edsair.doi.dedup.....c6cc221690e67f33fe455a1bdf6220c0