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1.
J Nutr Biochem ; 64: 198-205, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30530259

RESUMO

Fucoxanthin (Fx) and its biotransformed fucoxanthinol (FxOH) present strong anti-cancer effects in vitro and in vivo, however, the underlying mechanisms are not well known. We recently demonstrated that FxOH could induce anoikis-like cells in human colorectal cancer (CRC) cells. Thus, we developed molecular hallmarks for anoikis in vitro, and to confirm induction of such molecular hallmarks in an azoxymethane/ dextran sodium sulfate carcinogenic model by Fx ingestion. During the process of anoikis by FxOH (2.5 µmol/l) in DLD-1 cells, the cells show the characteristics of integrin ß1low/-, p-FAK(Tyr397)low/- or p-Paxillin(Tyr31)low/- cells with cleaved caspase-3high, which may be useful as molecular hallmarks. Fx administration (30 mg/kg body weight) significantly suppressed the number and size of polyps compared with untreated control mice. In addition, the incidence and multiplicity of colonic lesions tended to reduce. Moreover, cells showing integrin ß1low/-, p-FAK(Tyr397)low/- and p-Paxillin(Tyr31)low/- with cleaved caspase-3high in colonic crypts were significantly increased 2.2-, 4.8- and 5.2-fold by Fx administration compared with untreated control mice, respectively. Our results suggest that Fx showed a chemopreventive effect in the carcinogenic models through anoikis-like cells induction.


Assuntos
Anoikis/efeitos dos fármacos , Neoplasias Colorretais/prevenção & controle , Xantofilas/farmacologia , Animais , Anticarcinógenos/farmacologia , Azoximetano/toxicidade , Linhagem Celular Tumoral , Neoplasias Colorretais/metabolismo , Neoplasias Colorretais/patologia , Sulfato de Dextrana/toxicidade , Humanos , Integrina beta1/metabolismo , Mucosa Intestinal/efeitos dos fármacos , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Masculino , Camundongos Endogâmicos ICR , Paxilina/metabolismo , Proteínas/metabolismo
2.
Pathol Int ; 58(10): 652-6, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18801086

RESUMO

A 57-year-old woman was admitted to Hokkaido University Hospital because of dysphagia. Laryngoscopy indicated hypopharyngeal tumor histologically diagnosed as squamous cell carcinoma (SCC). A combination of radiotherapy and chemotherapy was performed for 2 months, and the hypopharyngeal lesion completely regressed. After 4 months, fever, anorexia, and malaise appeared, and chest X-ray and CT indicated two large tumors in the right lung. Transbroncheal lung biopsy (TBLB) specimens were diagnosed as SCC. Laboratory data showed high levels of serum granulocyte colony-stimulating factor (G-CSF) and parathyroid hormone-related protein (PTHrP). Subsequently, positron emission tomography (PET) showed multiple metastases to several organs including the liver, spine, skull, and thigh. Two months after readmission, the patient died with no success of chemotherapy. At autopsy, the lung tumor was clearly positive for both G-CSF and PTHrP on immunohistostaining. Retrospectively, examination showed that the primary pharyngeal tumor was focally positive for these two cytokines. Thus, a certain population of hypopharyngeal cancer producing G-CSF and PTHrP, spread to various organs and contributed to the rapid progression and poor prognosis. This case is presented with a discussion of several other cases in the literature.


Assuntos
Carcinoma de Células Escamosas/metabolismo , Fator Estimulador de Colônias de Granulócitos/sangue , Neoplasias Hipofaríngeas/metabolismo , Proteína Relacionada ao Hormônio Paratireóideo/sangue , Carcinoma de Células Escamosas/secundário , Carcinoma de Células Escamosas/terapia , Terapia Combinada , Transtornos de Deglutição/patologia , Evolução Fatal , Feminino , Humanos , Neoplasias Hipofaríngeas/patologia , Neoplasias Hipofaríngeas/terapia , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/secundário , Pessoa de Meia-Idade
3.
Neuroendocrinology ; 78(1): 1-11, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12869794

RESUMO

Urocortin II (Ucn II) is a novel corticotropin-releasing hormone (CRH)-related peptide discovered as a selective agonist for type-2 CRH receptor. In the rat or mouse brain, Ucn II mRNA shows weak expression mainly in the hypothalamic paraventricular nucleus (PVN) and the locus coeruleus (LC). Understanding the regulation of Ucn II mRNA expression under varying conditions provides new insights into central stress response. We examined expression of Ucn II mRNA in the PVN and LC following immobilization stress, water deprivation, and adrenalectomy. Rats subjected to immobilization stress exhibited a dramatic induction of Ucn II mRNA expression in the parvocellular part of the PVN at the end of 2 h of immobilization. In contrast, water deprivation for 3 days induced Ucn II mRNA expression mainly in the magnocellular part of the PVN. Although water-deprived rats showed a marked decrease in their food intake, pair-fed rats failed to alter PVN Ucn II mRNA expression, suggesting that osmotic stimuli per se, but not reduced food consumption during water deprivation, caused Ucn II mRNA induction in the magnocellular part of the PVN. Adrenalectomized rats failed to show an increase in Ucn II mRNA in the PVN when compared to sham-operated rats. Double-label in situ hybridization revealed colocalization of Ucn II mRNA in approximately 45% of the CRH mRNA-expressing cells in the parvocellular part of the PVN following immobilization, or colocalization in most of the vasopressin mRNA-expressing cells in the magnocellular part of the PVN following water deprivation. In the LC, no induction of Ucn II mRNA was observed in any of the three experimental conditions, indicating that the regulation of Ucn II mRNA expression was site-specific. The results show a stressor-specific regulation of Ucn II mRNA expression in the PVN and raise the possibility that Ucn II mRNA plays a modulatory role in stress-induced alteration of anterior and posterior pituitary function, depending on the type of stress.


Assuntos
Hormônio Liberador da Corticotropina/biossíntese , Núcleo Hipotalâmico Paraventricular/metabolismo , RNA Mensageiro/metabolismo , Estresse Psicológico/metabolismo , Adrenalectomia , Animais , Autorradiografia , Hormônio Liberador da Corticotropina/genética , Hormônio Liberador da Corticotropina/metabolismo , Ingestão de Alimentos , Retroalimentação Fisiológica , Imobilização , Hibridização In Situ , Locus Cerúleo/metabolismo , Osmose , Ratos , Ratos Wistar , Estresse Psicológico/etiologia , Urocortinas , Vasopressinas/metabolismo , Privação de Água
4.
Endocr J ; 49(6): 605-10, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12625409

RESUMO

A 27-year-old man was admitted to our hospital with facial erythema and general malaise. He had previously suffered from orbital myositis, central diabetes insipidus (DI), peripheral neuritis, and hypogonadotropic hypogonadism. Physical and immunological examinations revealed that he was suffering from systemic lupus erythematosus (SLE). Magnetic resonance imaging of the hypothalamic-pituitary region demonstrated a significant enlargement of the pituitary stalk and posterior pituitary. Endocrinological examinations showed that he had not only DI and hypogonadotropic hypogonadism but also hypoadrenalism and hypothyroidism, which were ascribed to the pituitary stalk lesion. Lymphocytic infundibuloneurohypophysitis associated with SLE was diagnosed. Administration of 30 mg/day of prednisolone for one month resulted in a marked reduction of the pituitary stalk thickening and posterior pituitary. It is recommended that a pharmacological dose of glucocorticoid be used in the treatment of lymphocytic hypophysitis patients who show significant thickening of the pituitary stalk and/or a large pituitary mass.


Assuntos
Doenças Hipotalâmicas/complicações , Lúpus Eritematoso Sistêmico/complicações , Doenças da Hipófise/complicações , Insuficiência Adrenal/diagnóstico , Insuficiência Adrenal/etiologia , Adulto , Diabetes Insípido/complicações , Diabetes Insípido/diagnóstico , Humanos , Hipogonadismo/diagnóstico , Hipogonadismo/etiologia , Doenças Hipotalâmicas/diagnóstico , Doenças Hipotalâmicas/tratamento farmacológico , Hipotireoidismo/diagnóstico , Hipotireoidismo/etiologia , Lúpus Eritematoso Sistêmico/diagnóstico , Linfócitos/patologia , Masculino , Doenças da Hipófise/diagnóstico , Doenças da Hipófise/tratamento farmacológico , Adeno-Hipófise/patologia , Neuro-Hipófise/patologia , Prednisolona/uso terapêutico , Resultado do Tratamento
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