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1.
J Pak Med Assoc ; 65(6): 597-601, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26060153

ABSTRACT

OBJECTIVE: To investigate the expression of cyclooxygenase-2 and cluster of differentiation 95 in renal cell carcinomas having different clinico-pathological characteristics. METHODS: The study entailed histopathological diagnoses carried out on paraffin blocks at the Department of Pathology of the Medical Hospital of Duzce University, Turkey, between 2005 and 2011. Immunohistochemical staining for cyclooxygenase-2 and cluster of differentiation 95was performed on tissue microarray using standard procedures. Each patient's age and gender as well as the tumour's grade, stage, diameter, ureteral surgical margins, vascular invasion, capsule invasion and subtype were assessed. In order to determine if the cases were still alive, relatives were telephoned and identity registration records were checked. SPSS 18 was used for statistical analysis. RESULTS: There were 49 paraffin blocks in the study.Significant correlations were found between cyclooxygenase-2 and tumour subtype (p=0.044) as well as between cyclooxygenase-2 and tumour diameter (p=0.026). There was a significant correlation between cluster of differentiation 95and the Fuhrman grade (p=0.050). CONCLUSIONS: Expression of cluster of differentiation 95and cyclooxygenase-2 may be correlated with prognostic parameters in renal cell carcinoma and may also be associated with tumour progression.


Subject(s)
Carcinoma, Renal Cell/metabolism , Cyclooxygenase 2/metabolism , Kidney Neoplasms/metabolism , fas Receptor/metabolism , Adult , Aged , Aged, 80 and over , Carcinoma, Renal Cell/mortality , Carcinoma, Renal Cell/pathology , Female , Humans , Immunohistochemistry , Kidney Neoplasms/mortality , Kidney Neoplasms/pathology , Male , Middle Aged , Neoplasm Grading , Neoplasm Staging , Prognosis , Tissue Array Analysis , Tumor Burden
2.
Turk J Med Sci ; 44(5): 839-43, 2014.
Article in English | MEDLINE | ID: mdl-25539555

ABSTRACT

AIM: Prostate cancer is the most commonly diagnosed malignancy and the second most common cause of cancer deaths in the Western male population. Matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) modulate the remodeling of the extracellular matrix (ECM). The imbalance between MMPs and TIMPs may lead to an emergence of pathological processes such as cancer. In this study, the association between TIMP-2 (-418 G/C) and MMP-2 (-1306 C/T) polymorphisms and prostate cancer in the Turkish population was investigated. MATERIALS AND METHODS: Sixty-one prostate cancer patients and 46 healthy subjects were included in the study. DNA was isolated from 2 mL of peripheral blood taken from subjects, and genotypes were analyzed by the polymerase chain reaction-restriction fragment length polymorphism method. RESULTS: The TIMP-2 -418 (GC) genotype was found in 15 cases (32.6%) in the control group and in 9 cases (14.8%) in the patients group, and statistical significance was determined (P = 0.037, OR = 0.346). The MMP-2 -1306 (CT) genotype was found 2.17 times more in the patient group than in the control group (P = 0.149, OR = 2.17). CONCLUSION: Our results show that the TIMP-2 -418 (GC) genotype had a putative protective effect against prostate cancer.


Subject(s)
Genetic Predisposition to Disease/genetics , Matrix Metalloproteinase 2/genetics , Polymorphism, Single Nucleotide , Prostatic Neoplasms/genetics , Tissue Inhibitor of Metalloproteinase-2/genetics , Aged , Aged, 80 and over , Genotype , Humans , Male , Middle Aged
3.
Asian Pac J Cancer Prev ; 14(9): 5107-10, 2013.
Article in English | MEDLINE | ID: mdl-24175784

ABSTRACT

BACKGROUND: Among women with haematuria, defining individuals under high risk for bladder cancer based on reproductive factors prior to cystoscopy would be of great benefit in the management of this condition. The aim of this study was to compare age and reproductive factors such as menopausal status, parity, age at first delivery and age at the last delivery between women who have haematuria with or without bladder cancer. MATERIALS AND METHODS: A total of 463 patients underwent diagnostic cystoscopy in Duzce University Faculty of Medicine between 1 June 2008 and 1 June 2013. Female patients who presented with persistent microscopic or macroscopic haematuria and underwent standard evaluation for haematuria including urinalysis, urine culture, urine cytology, urinary tract imaging with excretory urography or computerized tomography with contrast enhancement and endoscopic evaluation of the urethra and bladder were included in this study. Exclusion criteria were tobacco use and high risk occupations for bladder cancer such as textile, dry cleaning, painting and etc. Fourteen women had hematuria due to benign conditions, and 18 due to bladder cancer. Data were retrospectively retrieved from the medical records of Duzce University Hospital. RESULTS: Patients with haematuria due to benign reasons did not significantly differ from patients who were found to have bladder cancer in terms of age (p=0.28), menopausal status (p=0.29), mean parity (p=0.38), being nulliparous (p=0.57), parity ≥ 3 (p=0.22), age ≤ 18 years at first delivery (p=1.00), age ≥ 30 years at last delivery (p=0.26), age ≥ 35 years at last delivery (p=0.23) and percentage of the patients with advanced age (≥ 65 years) (p=0.18). CONCLUSIONS: It is difficult to predict a high risk for developing bladder cancer in women with haematuria based solely on reproductive factors.


Subject(s)
Carcinoma, Transitional Cell/epidemiology , Hematuria/epidemiology , Menopause , Parity , Reproductive History , Urinary Bladder Neoplasms/epidemiology , Adenocarcinoma/complications , Adenocarcinoma/diagnosis , Adenocarcinoma/epidemiology , Adult , Age Factors , Aged , Aged, 80 and over , Carcinoma, Transitional Cell/complications , Carcinoma, Transitional Cell/diagnosis , Cohort Studies , Cystoscopy , Female , Hematuria/diagnosis , Hematuria/etiology , Humans , Middle Aged , Retrospective Studies , Risk Assessment , Risk Factors , Sarcoma/complications , Sarcoma/diagnosis , Sarcoma/epidemiology , Tomography, X-Ray Computed , Urinalysis , Urinary Bladder Neoplasms/complications , Urinary Bladder Neoplasms/diagnosis
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