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1.
Int J Med Mushrooms ; 21(3): 225-235, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31002607

RESUMEN

A review of scientific information about the potential role of medicinal mushrooms in the prevention and treatment of gynecological cancers, human immunodeficiency virus, and human papillomavirus infections is reported here. The results of in vivo and in vitro experiments on 16 different species of Basidiomycetes and three Ascomycetes, which possess chemopreventive potential and are effective in clinical application in combination with chemotherapy, are also discussed. Medicinal mushroom extracts confirm an evident efficacy on the reduction of tumor cell proliferation and side effects in patients with gynecological tumors who are undergoing chemotherapy treatments. This review, the first on the use of medicinal mushrooms in the prevention and treatment of gynecological cancers, aims to highlight the remarkable potential of mushrooms in integrated oncology.


Asunto(s)
Agaricales/química , Productos Biológicos/uso terapéutico , Neoplasias de los Genitales Femeninos/tratamiento farmacológico , Neoplasias de los Genitales Femeninos/prevención & control , Animales , Antioxidantes/uso terapéutico , Ascomicetos/química , Basidiomycota/química , Productos Biológicos/química , Proliferación Celular/efectos de los fármacos , Ensayos Clínicos como Asunto , Femenino , VIH/efectos de los fármacos , Humanos , Ratones , Papillomaviridae/efectos de los fármacos , Neoplasias del Cuello Uterino/tratamiento farmacológico , Neoplasias del Cuello Uterino/prevención & control , Neoplasias Vaginales/tratamiento farmacológico , Neoplasias Vaginales/prevención & control
2.
J Korean Med Sci ; 16 Suppl: S42-53, 2001 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11748376

RESUMEN

The anticarcinogenic effects and mechanisms of the biotechnological drugs of Panax ginseng C.A. Meyer cultivated in Russia, bioginseng, panaxel and panaxel- 5, were studied. Bioginseng was produced from a tissue culture of ginseng root cultured on standard medium, whereas panaxel and panaxel-5 were produced from ginseng tissue root cultures using standard mediums enriched with 2-carboxyethylgermanium sesquioxide and 1-hydroxygermatran-monohydrate respectively. All three ginseng drugs inhibited the development of mammary tumors induced by intramammary injections of N-methyl-N-nitrosourea (MNU) in rats, the development of the brain and spinal cord tumors induced by transplacental administration of N-ethyl-N-nitrosourea (ENU) in rats, and the development of uterine, cervical and vaginal tumors induced by intravaginal applications of 7,12-dimethylbenz(a)anthracene (DMBA) in mice. The ginseng drugs induced the cytotoxic activity of macrophages in mice, enhanced T-lymphocyte rosette formation in guinea pigs exposed to cyclophosphamide, and stimulated the production of thyroid hormones in rats. These mechanisms may contribute to the anticarcinogenic action of the ginseng drugs. The organic germanium compounds present in panaxel and panaxel-5 did not potentiate the anticarcinogenic or immuno- stimulatory effects as much as biogeinseng. Preliminary clinical trials with panaxel and bioginseng were carried out in patients with precancerous lesions of the esophagus and endometrium. Panaxel was found to have a strong therapeutic effect in patients suffering from chronic erosive esophagitis. Bioginseng induced the regression of adenomatous-cystic hyperplasia of the endometrium in some patients. Thus, we conclude that the drugs of ginseng appear to hold considerable promise for future cancer chemoprevention.


Asunto(s)
Antineoplásicos Fitogénicos/uso terapéutico , Neoplasias Experimentales/prevención & control , Panax/metabolismo , Lesiones Precancerosas/prevención & control , Adenocarcinoma/inducido químicamente , Adenocarcinoma/prevención & control , Adulto , Animales , Células Cultivadas , Ensayos Clínicos como Asunto , Técnicas de Cultivo , Pruebas Inmunológicas de Citotoxicidad , Modelos Animales de Enfermedad , Neoplasias Endometriales/patología , Neoplasias Endometriales/prevención & control , Endometrio/patología , Neoplasias Esofágicas/patología , Neoplasias Esofágicas/prevención & control , Esófago/patología , Estradiol/sangre , Femenino , Fibroadenoma/inducido químicamente , Fibroadenoma/prevención & control , Humanos , Macrófagos Peritoneales/citología , Macrófagos Peritoneales/inmunología , Masculino , Neoplasias Mamarias Experimentales/inducido químicamente , Neoplasias Mamarias Experimentales/prevención & control , Ratones , Ratones Endogámicos C57BL , Neoplasias Experimentales/inducido químicamente , Neoplasias del Sistema Nervioso/inducido químicamente , Neoplasias del Sistema Nervioso/prevención & control , Lesiones Precancerosas/patología , Ratas , Neoplasias del Cuello Uterino/inducido químicamente , Neoplasias del Cuello Uterino/prevención & control , Neoplasias Uterinas/inducido químicamente , Neoplasias Uterinas/prevención & control , Neoplasias Vaginales/inducido químicamente , Neoplasias Vaginales/prevención & control
3.
Vopr Onkol ; 44(1): 79-85, 1998.
Artículo en Ruso | MEDLINE | ID: mdl-9578737

RESUMEN

The inhibitory effects of the newly-developed forms of beta-carotene--water-soluble and liposomal--have been studied in rats and mice bearing tumors induced in 4 models of carcinogenesis. Mammary tumors were induced by single injections of 1 mg methylnitrosourea into each gland. Esophageal tumors were induced in male rats by intragastric administration of 3 mg/kg methylbenzylnitrosoamine, thrice a week for 4 weeks. Tumors of the vagina and cervix uteri were induced by intravaginal painting with 25 mkg dimethylbenz(a)anthracene, twice a week for 6 weeks. Tumors of the lung were induced in female mice by intraperitoneal injection of 1 g/kg urethane, once a week for 6 weeks. With models I-III, animals received water-soluble beta-carotene (Aquiton-10) with drinking water (200 mg/I), on completion of carcinogen treatment and for another 9-12 months until the end of experiment. Urethane-treated mice received liposomal beta-carotene with drinking water (60 mg/l) 10 days before the beginning of carcinogen treatment and for another 6 months until the end experiment. Water-soluble beta-carotene failed to influence the carcinogenesis in the mammary gland and esophagus in rats; however, it significantly inhibited carcinoma development in murine vagina and cervix uteri (47.0%). Liposomal beta-carotene significantly inhibited lung adenomas (46.4%) and mammary carcinomas (55.6%) in urethane-treated mice.


Asunto(s)
Anticarcinógenos/uso terapéutico , Neoplasias Experimentales/prevención & control , beta Caroteno/uso terapéutico , Animales , Anticarcinógenos/administración & dosificación , Neoplasias Esofágicas/prevención & control , Femenino , Liposomas , Neoplasias Pulmonares/prevención & control , Masculino , Neoplasias Mamarias Experimentales/prevención & control , Ratones , Neoplasias Experimentales/inducido químicamente , Ratas , Solubilidad , Neoplasias del Cuello Uterino/prevención & control , Neoplasias Vaginales/prevención & control , Agua , beta Caroteno/administración & dosificación
4.
Biull Eksp Biol Med ; 116(11): 534-6, 1993 Nov.
Artículo en Ruso | MEDLINE | ID: mdl-8312554

RESUMEN

The anticarcinogenic effects of bioginseng and two germanium-selective drugs produced by cultivating cells of ginseng radix (Panax ginseng C. A. Mey) in a conventional medium or in media containing organogermanium compounds were studied. Squamous-cell carcinomas of the uterus cervix and vagina were induced by intravaginal applications of 7,12-dimethylbenz(a)anthracene in mice. The drugs of ginseng were used orally or intravaginally during a long period of time of the postinitiation stage of carcinogenesis. All the drugs used locally effectively inhibited the development of induced carcinomas of the uterus cervix and vagina. When orally used, the drugs of ginseng exhibited only an insignificant tendency to inhibit the carcinogenesis of uterus cervix and vagina. The anticarcinogenic effects of the compared drugs were similar.


Asunto(s)
Anticarcinógenos/administración & dosificación , Panax , Plantas Medicinales , Lesiones Precancerosas/prevención & control , Neoplasias del Cuello Uterino/prevención & control , Neoplasias Vaginales/prevención & control , 9,10-Dimetil-1,2-benzantraceno , Animales , Células Cultivadas , Distribución de Chi-Cuadrado , Ensayos de Selección de Medicamentos Antitumorales , Femenino , Germanio/farmacología , Ratones , Ratones Endogámicos , Compuestos Organometálicos/farmacología , Panax/efectos de los fármacos , Extractos Vegetales/administración & dosificación , Lesiones Precancerosas/inducido químicamente , Lesiones Precancerosas/mortalidad , Neoplasias del Cuello Uterino/inducido químicamente , Neoplasias del Cuello Uterino/mortalidad , Neoplasias Vaginales/inducido químicamente , Neoplasias Vaginales/mortalidad
5.
Vopr Onkol ; 39(7-12): 291-5, 1993.
Artículo en Ruso | MEDLINE | ID: mdl-7825300

RESUMEN

The paper reports the results of the experimental and clinical evaluation of the administration of drugs prepared from flowers of Filipendula ulmaria (L.) Maxim for cervical dysplasia and cancer treatment. Local administration of decoction resulted in a 39% drop in the frequency of squamous-cell carcinoma of the cervix and vagina induced in mice by 7,12-dimethyl-benz(a)anthracene treatment. Positive response was recorded in 32 patients (67%), including 25 cases (52%) of complete regression of dysplasia, out of 48 cases of cervical dysplasia treated with courses of ointment application. No recurrence was observed in 10 completely cured patients within 12 months.


Asunto(s)
Carcinoma de Células Escamosas/prevención & control , Extractos Vegetales/uso terapéutico , Plantas Medicinales , Displasia del Cuello del Útero/tratamiento farmacológico , Neoplasias del Cuello Uterino/prevención & control , Neoplasias Vaginales/prevención & control , Administración Intravaginal , Animales , Benzo(a)Antracenos , Carcinoma de Células Escamosas/inducido químicamente , Femenino , Humanos , Ratones , Ratones Pelados , Extractos Vegetales/administración & dosificación , Neoplasias del Cuello Uterino/inducido químicamente , Neoplasias Vaginales/inducido químicamente
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