ABSTRACT
Ovarian cancer is one of the most malignant genital cancers, with a high mortality rate. Many researchers have suggested that matrix metalloproteinases (MMPs) have remarkably high expression in ovarian cancer tissues. MMPs are considered to be related to the occurrence, development, invasion and metastasis of ovarian cancer. Moreover, some studies have discovered that the unbalance between MMPs and tissue inhibitor of metalloproteinases (TIMPs) are associated with the malignant phenotype of tumors. This review summarizes the latest research progress of MMPs in ovarian cancer. The investigation of MMP mechanism in ovarian cancer will facilitate the development of effective anti-tumor drugs, and thereby improve the survival rate of patients with ovarian cancer.
Subject(s)
Humans , Female , Biomarkers, Tumor/metabolism , Matrix Metalloproteinases/metabolism , Ovarian Neoplasms/enzymology , Gene Expression/genetics , Matrix Metalloproteinase Inhibitors/metabolism , Matrix Metalloproteinases/genetics , Ovarian Neoplasms/genetics , Ovarian Neoplasms/secondary , Tissue Inhibitor of Metalloproteinases/metabolismSubject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Female , Humans , Middle Aged , /metabolism , Dysgerminoma/enzymology , Hypercalcemia/enzymology , Hypercalcemia/etiology , Ovarian Neoplasms/enzymology , Ovary/enzymology , /genetics , /metabolism , Dysgerminoma/genetics , Dysgerminoma/pathology , Macrophages/enzymology , Macrophages/pathology , Membrane Glycoproteins/metabolism , Ovarian Neoplasms/genetics , Ovarian Neoplasms/pathology , Reverse Transcriptase Polymerase Chain Reaction , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Cell Surface/metabolism , Toll-Like ReceptorsABSTRACT
INTRODUCTION: Ovarian cancer is generally diagnosed at advanced stages of the disease; therefore, poor prognoses are typical. The development of tumor markers is thus of utmost importance. Prostasin is a protease that in normal tissues is highly expressed only in the prostate gland and seminal fluid. A previous study showed that prostasin is highly overexpressed in ovarian cancer cell lines. This study sought to evaluate the expression of prostasin in ovarian cancer. METHODS: Fresh tumor samples of ovarian epithelial cancer (n: 12) were analyzed for expression of prostasin mRNA (messenger ribonucleic acid) by conventional and real time quantitative PCR (polymerase chain reaction). As a standard control, a normal prostate sample was analyzed. RESULTS: Using conventional PCR, prostasin was detected in all but one sample. Using quantitative PCR, prostasin was over-expressed in all but one of the samples as compared to the control (prostate). CONCLUSIONS: These findings indicate that prostasin is overexpressed in many epithelial ovarian cancers. Further studies of prostasin as a potential biomarker for this disease are warranted.
Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Middle Aged , Gene Expression Regulation, Neoplastic , Mass Screening/methods , Neoplasm Proteins/blood , Ovarian Neoplasms/enzymology , Serine Endopeptidases/blood , Biomarkers, Tumor/blood , Ovarian Neoplasms/diagnosis , Pilot Projects , Reverse Transcriptase Polymerase Chain ReactionABSTRACT
To investigate the expression of cyclooxygenase-2 (COX-2) in ovarian cancer cell lines, RT-PCR and immunocytochemistry were used to detect the expression of COX-2 in 5 ovarian cancer cell lines. The expression of COX-2 mRNA and protein was detected in all 5 cell lines. It is suggested that COX-2 is expressed in ovarian cancer cell lines, which provides a basis for the chemoprevention of ovarian cancer.
Subject(s)
Cell Line, Tumor , Cyclooxygenase 2/genetics , Cyclooxygenase 2/metabolism , Ovarian Neoplasms/enzymology , Ovarian Neoplasms/pathology , RNA, Messenger/genetics , RNA, Messenger/metabolismABSTRACT
The serum phosphohexose isomerase (PHI), aldolase and hexokinase activities have been determined in 36 patients of carcinoma ovary with different clinical stages and in 25 healthy normal female subjects. The serum PHI and hexokinase levels were significantly elevated (P less than .001) in all the stages of malignancy while serum aldolase was significantly elevated only in stages III and IV of malignancy. The enzyme levels showed statistically significant response to therapy in stage II patients. The mean values in patients with progression of the disease were not significantly different.