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2.
PLoS One ; 14(6): e0218986, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31251767

RESUMO

In unilateral ureteral obstruction (UUO), both oxidative stress and mitochondrial dysfunction are related to cell death. The aim of this study has been to characterize profiles of enzyme antioxidant activities and mitochondrial functioning of the contralateral (CL) compared to UUO and Sham (false-operated) kidneys of Balb/c mice. Kidneys were resected 14 days after obstruction for immunohistochemical and cortical mitochondrial functioning assays. Antioxidant enzymes activities were investigated in mitochondria and cytosol. Oxygen consumption (QO2) and formation of O2 reactive species (ROS) were assessed with pyruvate plus malate or succinate as the respiratory substrates. QO2 decreased in CL and UUO in all states using substrates for complex II, whereas it was affected only in UUO when substrates for complex I were used. Progressive decrease in mitochondrial ROS formation-in the forward and reverse pathway at complex I-correlates well with the inhibition of QO2 and, therefore, with decreased electron transfer at the level of complexes upstream of cytochrome c oxidase. CL and UUO transmembrane potential responses to ADP were impaired with succinate. Intense Ca2+-induced swelling was elicited in CL and UUO mitochondria. Important and selective differences exist in CL antioxidant enzymes with respect to either Sham or UUO kidneys: CL kidneys had increased mitochondrial glutathione peroxidase and cytosolic catalase activities, indicative of compensatory responses in the face of an early altered ROS homeostasis (as detected by 4-hydroxynonenal), and of a significant tendency to apoptosis. In CL and UUO, upregulation of nuclear (erythroid-derived 2)-like 2 transcription factor (Nrf2), as well as of cytoplasmic and nuclear Kelch-like ECH-associated protein 1 (Keap1) in opposition to decreased heme oxygenase-1 (HO-1), suggest impairment of the Nrf2/Keap1/HO-1 system. It is concluded that chronic obstruction impairs mitochondrial function in CL and UUO, preferentially affecting complex II.


Assuntos
Rim/citologia , Mitocôndrias/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Obstrução Ureteral/cirurgia , Animais , Sinalização do Cálcio , Catalase/metabolismo , Modelos Animais de Doenças , Glutationa Peroxidase/metabolismo , Homeostase , Rim/metabolismo , Rim/cirurgia , Masculino , Camundongos , Oxirredução , Regulação para Cima , Obstrução Ureteral/etiologia , Obstrução Ureteral/metabolismo
3.
Nutr Cancer ; 65(7): 1076-85, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24053141

RESUMO

Prostate cancer is the most common malignancy in men and the second leading cause of cancer-related mortality in men of the Western world. Lycopene has received attention because of its expcted potential to prevent cancer. In the present study, we evaluated the influence of lycopene on cell viability, cell cycle, and apoptosis of human prostate cancer cells and benign prostate hyperplastic cells. Using MTT assay, we observed a decrease of cell viability in all cancer cell lines after treatment with lycopene, which decreased the percentage of cells in G0/G1 phase and increased in S and G2/M phases after 96 h of treatment in metastatic prostate cancer cell lineages. Flow citometry analysis of cell cycle revealed lycopene promoted cell cycle arrest in G0/G1 phase after 48 and 96 h of treatment in a primary cancer cell line. Using real time PCR assay, lycopene also induced apoptosis in prostate cancer cells with altered gene expression of Bax and Bcl-2. No effect was observed in benign prostate hyperplasia cells. These results suggest an effect of lycopene on activity of human prostate cancer cells.


Assuntos
Apoptose/efeitos dos fármacos , Carotenoides/farmacologia , Sobrevivência Celular/efeitos dos fármacos , Fase G1/efeitos dos fármacos , Fase G2/efeitos dos fármacos , Hiperplasia Prostática/patologia , Neoplasias da Próstata/patologia , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Expressão Gênica , Humanos , Licopeno , Masculino , Hiperplasia Prostática/metabolismo , Neoplasias da Próstata/metabolismo , Proteína X Associada a bcl-2/genética , Proteína X Associada a bcl-2/metabolismo
4.
Int J Surg Pathol ; 19(4): 476-86, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21878477

RESUMO

Solitary fibrous tumor (SFT) of the central nervous system was first described in 1996. A number of cases have been reported since. The authors present 5 new cases: 4 intracranial and 1 intraspinal. All patients were adults (age range, 47 to 75 years); 4 were male and 1 female; 4 cases were primary tumors; and 1 was a second tumor recurrence. All patients were surgically treated with gross total removal. All cases were histologically examined with immunohistochemical confirmation; 2 tumors exhibited diffuse classic histology, 1 tumor was a cellular variant, 1 tumor was myxoid, and 1 was predominantly classic with focal myxoid features and focally pleomorphic. The postoperative course was uneventful in all. The patient with the cellular variant experienced 2 local recurrences and eventually died of disease 10 years after the initial diagnosis. The patient with the myxoid variant--the tumor studied--which was the second recurrence of a previously misdiagnosed fibrous meningioma surgically treated 15 years earlier, had a recurrence after 2 years for the third time and eventually died of disease. Three patients are alive and well 11.6, 6, and 4 years after surgery. SFT is a rare tumor that needs to be differentiated from some mimickers, mainly fibrous meningioma, hemangiopericytoma, and with regard to the myxoid variant, also adult-onset myxochordoid meningioma and myxoid peripheral nerve sheath tumor. Immunohistochemistry is crucial for the correct diagnosis of SFT. The authors also performed a review of the literature and found a little more than 200 cases on record.


Assuntos
Neoplasias Encefálicas/patologia , Tumores Fibrosos Solitários/patologia , Neoplasias da Medula Espinal/patologia , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
5.
Adv Anat Pathol ; 18(5): 356-92, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21841406

RESUMO

We reviewed the world literature on solitary fibrous tumors of the central nervous system from August 1996 to July 2011, focusing on both clinicopathological features and diagnostic findings. The anatomical distribution of the 220 cases reported so far reveals that most are intracranial and just over one-fifth are intraspinal. In decreasing frequency, intracranial tumors involve the supratentorial and infratentorial compartments, the pontocerebellar angle, the sellar and parasellar regions, and the cranial nerves. Intraspinal tumors are mainly located in the thoracic and cervical segments. Although most solitary fibrous tumors of the central nervous system are dural based, a small subset presents as subpial, intraparenchymal, intraventricular, or as tumors involving the nerve rootlets with no dural connection. Preoperative imaging and intraoperative findings suggest meningioma, schwannoma or neurofibroma, hemangiopericytoma, or pituitary tumors. Immunohistochemistry is critical to establish a definitive histopathological diagnosis. Vimentin, CD34, BCL2, and CD99 are the most consistently positive markers. The usual histologic type generally behaves in a benign manner if complete removal is achieved. Recurrence is anticipated when resection is subtotal or when the tumor exhibits atypical histology. The proliferative index as assessed by MIB1 labeling is of prognostic significance. Occasionally, tumors featuring conventional morphology may recur, perhaps because of minimal residual disease left behind during surgical extirpation. Rare extracranial metastases and tumor-related deaths are on record. Surgery is the treatment of choice. Stereotactic and external beam radiation therapy may be indicated for postsurgical tumor remnants and for unresectable recurrences. Long-term active surveillance of the patients is mandatory.


Assuntos
Neoplasias Encefálicas/diagnóstico , Tumores Fibrosos Solitários/diagnóstico , Neoplasias da Medula Espinal/diagnóstico , Biomarcadores Tumorais/metabolismo , Neoplasias Encefálicas/metabolismo , Neoplasias Encefálicas/cirurgia , Proliferação de Células , Feminino , Humanos , Masculino , Recidiva Local de Neoplasia , Radioterapia Adjuvante , Tumores Fibrosos Solitários/metabolismo , Tumores Fibrosos Solitários/cirurgia , Neoplasias da Medula Espinal/metabolismo , Neoplasias da Medula Espinal/cirurgia
6.
San José; Porvenir; 2. ed; 1997. 167 p.
Monografia em Espanhol | LILACS | ID: lil-238239
7.
Rev. Col. Bras. Cir ; 18(2): 47-50, mar.-abr. 1991. ilus
Artigo em Português | LILACS | ID: lil-98762

RESUMO

No periodo de julho de l985 a novembro de 1989 foram tratados em nosso Serviço, 11 casos de esclerose de colo vesical, sendo nove (82%) apos prostatectomia transvesical e dois (18%) apos ressecçao transuretral da prostata. O diagnostico foi firmado pela avaliaçao dos sintomas obstrutivos presentes apos uma cirurgia prostatica, pela uretroscopia e pela uretrocistografia retrograda. Foram utilizadas duas tecnicas para o tratamento da esclerose do colo vesical: ressecçao transuretral do colo vesical em sete casos (64%) e incisao do colo vesical com a Faca de Sachse em quatro casos (36%). Os resultados foram considerados bons em 86%, quando utilizada a ressecçao transuretral do colo vesical, e em 75% dos casos, quando utilizada a incisao do colo vesical com a Faca de Sachse


Assuntos
Obstrução do Colo da Bexiga Urinária/cirurgia , Obstrução do Colo da Bexiga Urinária/diagnóstico , Obstrução do Colo da Bexiga Urinária , Próstata/cirurgia
8.
Folha méd ; 101(3): 145-6, set. 1990. ilus
Artigo em Português | LILACS | ID: lil-113504

RESUMO

O comprometimento retal pelo adenocarcinoma da próstata ocorre em aproximadamente 10% dos casos. A fístula vésico-retal devida à extensäo direta do carcinoma prostático é uma condiçäo patológica bastante rara. É relatado um caso desta rara complicaçäo e säo discutidos seus aspectos urológicos, proctológicos e radiológicos


Assuntos
Idoso , Humanos , Masculino , Adenocarcinoma/complicações , Fístula Retal/etiologia , Fístula da Bexiga Urinária/etiologia , Neoplasias da Próstata/complicações
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