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1.
Drug Des Devel Ther ; 8: 2089-97, 2014.
Article in English | MEDLINE | ID: mdl-25364234

ABSTRACT

The aims of this study conducted on rats were to determine mast cell (MC) proliferation on undescended testes (UDTs); whether there is a correlation between MC proliferation and testicular damage; and whether testicular damage can be prevented with administration of an MC blocker. Sixty-five newborn male rats were divided into three groups. During the neonatal period, unilateral UDTs were experimentally induced in Group 2 and Group 3. The rats in Group 3 were given 1 mg/kg/day ketotifen orally until the end of the study. Groups 2 (n=30) and 3 (n=15) were divided into groups of ten and five rats, respectively, each of which underwent bilateral orchiectomy in either the prepubertal, pubertal, or adult period. Group 1 (n=15) underwent a sham operation followed by bilateral orchiectomy, with five rats in each of the prepubertal, pubertal, and adult periods. Testicular MCs in the interstitial and subtubular areas, biopsy scores, interstitial connective tissue, seminiferous tubule (ST) diameters, and the basement membrane thickness of STs were evaluated. In Group 2 the ST diameters in the UDTs decreased, the number of MCs in the interstitial and subtubular areas increased, ST basement membranes thickened, and spermatogenesis decreased. The number of MCs in the interstitial and subtubular areas of the descended testes increased and spermatogenesis decreased. In Group 3, the number of MCs in the interstitial and subtubular areas decreased. In unilateral UDTs, the number of MCs in the interstitial and subtubular areas increased in both testes. Fibrosis developed in the ST basement membranes and interstitial areas, and spermatogenesis deteriorated. Testicular fibrosis may be prevented with administration of an MC blocker.


Subject(s)
Cryptorchidism/drug therapy , Cryptorchidism/pathology , Ketotifen/pharmacology , Testis/drug effects , Animals , Animals, Newborn , Cell Proliferation/drug effects , Disease Models, Animal , Male , Mast Cells/drug effects , Mast Cells/pathology , Rats , Rats, Wistar , Spermatogenesis/drug effects , Testis/pathology
2.
Pathol Res Pract ; 205(12): 854-7, 2009.
Article in English | MEDLINE | ID: mdl-19762163

ABSTRACT

Angiogenesis is a multistep process that depends on the balance of proangiogenic factors and inhibitors as well as on interactions with the extracellular matrix. We examined the immunohistochemical expression of the defining angiogenic agents, vascular endothelial growth factor (VEGF) and matrix metalloproteinase-9 (MMP-9), and the antiangiogenic agent thrombospondin-1 (TSP-1) in 131 patients with urothelial carcinoma and correlated their expression levels with clinicopathological parameters. VEGF and MMP-9 expression was higher in high-grade tumors than in low-grade tumors (p=0.000 and p=0.001, respectively), whereas the reverse was true for TSP-1 (p=0.000). VEGF and MMP-9 expression was higher in deeper tumors compared to superficial tumors and in invasive tumors compared to non-invasive tumors (p=0.001 and p=0.001, respectively), while TSP-1 was lower (p=0.000). We could differentiate 22 of 41 muscle-invasive (T2) cases as superficial (T2a; n=7) or deep (T2b; n=15), but no difference was found between them regarding VEGF, MMP-9, or TSP-1 expression (p=0.783, p=0.289, and p=0.783, respectively). There was a positive correlation between VEGF and MMP-9 expression (p=0.008, r=0.23) but a negative correlation between MMP-9 and TSP-1 expression (p=0.014, r=-0.21). Increased VEGF and MMP-9 expression as well as decreased TSP-1 expression may play considerable roles in the invasion and differentiation of urothelial carcinoma.


Subject(s)
Carcinoma/chemistry , Matrix Metalloproteinase 9/analysis , Thrombospondin 1/analysis , Urinary Bladder Neoplasms/chemistry , Urothelium/chemistry , Vascular Endothelial Growth Factor A/analysis , Adult , Aged , Aged, 80 and over , Carcinoma/blood supply , Carcinoma/enzymology , Carcinoma/pathology , Cell Differentiation , Female , Humans , Immunohistochemistry , Male , Middle Aged , Neoplasm Invasiveness , Neoplasm Staging , Urinary Bladder Neoplasms/blood supply , Urinary Bladder Neoplasms/enzymology , Urinary Bladder Neoplasms/pathology , Urothelium/blood supply , Urothelium/enzymology , Urothelium/pathology , Young Adult
3.
Pathol Res Pract ; 203(8): 625-7, 2007.
Article in English | MEDLINE | ID: mdl-17662539

ABSTRACT

The coexistence of renal cell carcinoma and non-Hodgkin's lymphoma is more common than expected in the general population; however, renal cell carcinoma with infiltration by non-Hodgkin's lymphoma has rarely been reported. Here we report on a 77-year-old patient who presented with small lymphocytic lymphoma in the jugulodigastric lymph node. He underwent nephrectomy for a renal mass 5 months later. On histopathological examination, the mass was diagnosed as a grade III renal cell carcinoma with infiltrated small lymphocytic lymphoma that was positive for B-cells (CD20). This case is discussed in terms of the coexistence of these tumors and tumor to tumor metastasis.


Subject(s)
Carcinoma, Renal Cell/pathology , Kidney Neoplasms/pathology , Lymphoma, B-Cell/pathology , Neoplasms, Multiple Primary/pathology , Aged , Antigens, CD20/metabolism , Carcinoma, Renal Cell/metabolism , Humans , Immunohistochemistry , Kidney Neoplasms/metabolism , Lymphoma, B-Cell/metabolism , Male , Neoplasms, Multiple Primary/metabolism
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