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1.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 531-534, 2015.
Artículo en Inglés | WPRIM | ID: wpr-250383

RESUMEN

This study aimed to evaluate the effects of Pin1 inhibitor Juglone on proliferation, migration and the angiogenic ability of breast cancer cell line MCF7Adr. MCF7Adr cells were cultured and separately treated with Pin1 inhibitor Juglone (treatment group) and DMEM without drug (control group). The cell cycle was examined by flow cytometry. Cell migration was measured by wound-healing assay. Cyclin E protein content was detected by Western blotting. The angiogenesis factor vascular endothelial growth factor (VEGF) in cell media was determined by enzyme linked immunosorbent assay. The results showed that the percentage of cells in G2/M phase in treatment group was significantly higher than that in control group (25.5% vs. 10.1%, P<0.05), and that in G0/G1 phase and S stage in treatment group was significantly lower than that in control group (40.5% vs. 48.2%, and 33.7% vs. 41.7%, P<0.05). Cyclin E protein content in treatment group was significantly lower than that in control group (39.2 ± 7.4 vs. 100 ± 23.1, P<0.05). (A0-A24)/A0 value in treatment group was significantly lower than that in control group (23.9 ± 3.8 vs. 100 ± 14.4, P<0.05). VEGF-A, -B, and -C contents in cell media of treatment group were significantly lower than those in control group (P<0.05). It was suggested that Pin1 inhibitor Juglone can effectively inhibit the proliferation, migration and the angiogenic ability of MCF7Adr cells, and can be used as an alternative drug therapy for breast cancer.


Asunto(s)
Femenino , Humanos , Antineoplásicos , Farmacología , Neoplasias de la Mama , Quimioterapia , Metabolismo , Ciclo Celular , Movimiento Celular , Proliferación Celular , Ciclina E , Metabolismo , Regulación Neoplásica de la Expresión Génica , Células MCF-7 , Peptidilprolil Isomerasa de Interacción con NIMA , Naftoquinonas , Farmacología , Isomerasa de Peptidilprolil , Factor A de Crecimiento Endotelial Vascular , Metabolismo
2.
Chinese Journal of Contemporary Pediatrics ; (12): 496-501, 2015.
Artículo en Chino | WPRIM | ID: wpr-346119

RESUMEN

<p><b>OBJECTIVE</b>To explore the effect of silence of Pin1 expression on hyperoxia-induced apoptosis in alveolar epithelial cells A549.</p><p><b>METHODS</b>A549 cells were divided into four groups: control, hyperoxia, negative lentivirus and Pin1-shRNA hyperoxia. The hyperoxia group was exposed to a mixture of 95%O2 and 5%CO2 for 10 minutes. Then cells were cultured in a closed environment. After 24 hours, the changes of morphology were observed under an inverted microscope. Cell apoptosis was detected by flow cytometry (FCM). The expression of X-linked inhibitor of apoptosis protein (XIAP) and Caspase-9 were detected by immunohistochemistry. The production of reactive oxygen species (ROS) and cellular mitochondria membrane potential (△Ψm) were determined by fluorescence microscopy.</p><p><b>RESULTS</b>Under the inverted microscope, the A549 cells grew slowly and the changes in morphology of the cells were most obvious in the hyperoxia and negative lentivirus groups. The changes in morphology of A549 cells were obviously improved in the Pin1-shRNA hyperoxia group. The FCM results showed that the apoptosis rate of A549 cells increased, Caspase-9 expression increased, XIAP expression decreased, mitochondrial ROS production increased and mitochondrial membrane potential decreased in the hyperoxia and negative lentivirus groups compared with the control group (P<0.05). Compared with the hyperoxia and negative lentivirus groups, the apoptosis rate of A549 cells decreased, Caspase-9 expression decreased, XIAP expression increased, mitochondrial ROS production decreased and mitochondrial membrane potential increased in the Pin1-shRNA hyperoxia group (P<0.05), although the levels of the indexes did not reach to those of the control group.</p><p><b>CONCLUSIONS</b>Silencing of Pin1 could suppress hyperoxia-induced apoptosis of A549 cells.</p>


Asunto(s)
Humanos , Apoptosis , Caspasa 9 , Genética , Hiperoxia , Patología , Potencial de la Membrana Mitocondrial , Peptidilprolil Isomerasa de Interacción con NIMA , Isomerasa de Peptidilprolil , Fisiología , Especies Reactivas de Oxígeno , Metabolismo , Proteína Inhibidora de la Apoptosis Ligada a X , Genética
3.
Acta Pharmaceutica Sinica ; (12): 854-860, 2014.
Artículo en Chino | WPRIM | ID: wpr-245003

RESUMEN

This study is to explore new lead compounds by inhibition of Pin1 for anticancer therapy using temperature sensitive mutants. As Pin1 is conserved from yeast to human, we established a high-throughput screening method for Pin1 inhibitors, which employed yeast assay. This method led to the identification of one potent hits, 8-11. In vitro, 8-11 inhibited purified Pin1 enzyme activity with IC50 of (10.40 +/- 1.68) micromol x L(-1), induced G1 phase arrest and apoptosis, showed inhibitory effects on a series of cancer cell proliferation, reduced Cyclin D1 expression, was defined as reciprocally matched for protein-ligand complex in virtual docking analysis and reduced cell migration ability. In vivo, we could observe reduction of tumor volume after treatment with 8-11 in xenograft mice compared with vehicle DMSO treatment. Altogether, these results provide for the first time the involvement of 8-11 in the anticancer activity against Pin1.


Asunto(s)
Animales , Humanos , Ratones , Apoptosis , Proliferación Celular , Ciclina D1 , Metabolismo , Ensayos de Selección de Medicamentos Antitumorales , Métodos , Fase G1 , Ensayos Analíticos de Alto Rendimiento , Métodos , Peptidilprolil Isomerasa de Interacción con NIMA , Neoplasias , Patología , Isomerasa de Peptidilprolil , Temperatura , Ensayos Antitumor por Modelo de Xenoinjerto , Levaduras
4.
Acta Pharmaceutica Sinica ; (12): 1266-1272, 2013.
Artículo en Chino | WPRIM | ID: wpr-259484

RESUMEN

Pin1 (peptidyl-prolyl cis-trans isomerase NIMA-interacting 1) belongs to peptidyl-prolyl cis-trans isomerase (PPIase) and is a novel promising anticancer target. Based on the lead structure of benzophenone, a series of novel diarylether derivatives containing a pyrimidine ring were designed and synthesized. The inhibitory activities on Pin1 of compounds 5a-5d and 6a-6i were evaluated by a protease-coupled enzyme assay. Of all the evaluated compounds, 6 compounds displayed inhibitory activities. Molecular docking was performed using FlexX algorithm to explore the binding mode of the active molecules.


Asunto(s)
Humanos , Diseño de Fármacos , Inhibidores Enzimáticos , Química , Farmacología , Éteres , Química , Farmacología , Concentración 50 Inhibidora , Simulación del Acoplamiento Molecular , Estructura Molecular , Peptidilprolil Isomerasa de Interacción con NIMA , Isomerasa de Peptidilprolil , Metabolismo , Pirimidinas , Química , Relación Estructura-Actividad
5.
Journal of Southern Medical University ; (12): 1403-1406, 2013.
Artículo en Chino | WPRIM | ID: wpr-319402

RESUMEN

<p><b>OBJECTIVE</b>To investigate the clinicopathologic significance of pin1 and PR in patients with endometrial adenocarcinoma.</p><p><b>METHODS</b>The expression of pin1 and PR were investigated by immunohistochemistry in a total of 50 endometrial adenocarcinoma specimens.</p><p><b>RESULTS</b>Pin1 was over expressed in 66% (33/50) of the cases. The expression rate decreased gradually with tumor differentiation(P<0.05). In addition, pin1 expression was negatively correlated with lymph node metastasis and invasive depth of myometrium. Moreover, pin1 was positively correlated with PR expression.</p><p><b>CONCLUSION</b>Our results suggest that pin1 may play important roles in the tumorigenesis and migration of endometrial cancer. Pin1 expression may be considered as a prognostic marker as PR in patients with endometrial cancer.</p>


Asunto(s)
Adulto , Femenino , Humanos , Persona de Mediana Edad , Biomarcadores de Tumor , Metabolismo , Neoplasias Endometriales , Metabolismo , Patología , Metástasis Linfática , Peptidilprolil Isomerasa de Interacción con NIMA , Isomerasa de Peptidilprolil , Metabolismo , Receptores de Progesterona , Metabolismo , Neoplasias Uterinas , Metabolismo , Patología
6.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1112-1115, 2009.
Artículo en Chino | WPRIM | ID: wpr-746692

RESUMEN

OBJECTIVE@#To study the expression and relationship of Pin1 and CyclinD1 in adult papilloma of larynx, and the effect of both in laryngeal papilloma's canceration.@*METHOD@#Ninety-two cases of paraffin section with immunoperoxidase (SP) staining method was used to detect the distribution of Pin1 and CyclinD1 in 10 cases of laryngeal normal epithelial tissue, 39 cases of laryngeal papilloma, 27 cases of laryngeal papilloma with middle, severe atypical hyperplasia and 16 cases of laryngeal carcinoma.@*RESULT@#The distribution of Pin1 and CyclinD1 increased gradually from laryngeal normal epithelial tissue to laryngeal carcinoma (P0.0125), but there had significant difference of the expression of Pin1 and CyclinD1 among the rest groups; There was significantly direct correlation between the expression of Pin1 and CyclinD1 (P<0.05).@*CONCLUSION@#The hyper-expressions of Pin1 and CyclinD1 may play a key role in laryngeal papilloma's malignant change. Pin1 up-regulating the expressions of cyclinD1 possibly participate in its malignant change.


Asunto(s)
Adulto , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Ciclina D1 , Metabolismo , Neoplasias Laríngeas , Metabolismo , Patología , Peptidilprolil Isomerasa de Interacción con NIMA , Papiloma , Metabolismo , Patología , Isomerasa de Peptidilprolil , Metabolismo
7.
Journal of Central South University(Medical Sciences) ; (12): 63-66, 2009.
Artículo en Chino | WPRIM | ID: wpr-814250

RESUMEN

OBJECTIVE@#To investigate the effect of yizhi jiannao granule concentration fluid (YCF) on the expression of peptidyl-prolyl-cis-trans isomerase A (Pin1) and high mobility group box 1 (HMGB1) mRNA in the hippocampus of senescence accelerated mice Senile-Prone8(SAMP8).@*METHODS@#Six-month old SAMP8 mice were randomly divided into a YCF group and a model group. Six-month old SAMP8 mice were served as a normal control group. The YCF group was ravaged, while the model group and the normal control group were gavaged with double-distilled water for 8 weeks. The hippocampus was taken out for examination. The expression of Pin1 and HMGB1 mRNA was measured by RT-PCR.@*RESULTS@#In the YCF group, the level of Pin1 mRNA increased, and the level of HMGB1 mRNA decreased compared with that of the model group.@*CONCLUSION@#Yizhi jiannao granules can prevent Alzheimer's disease by increasing the Pin1 level and decreasing the HMGB1 level.


Asunto(s)
Animales , Masculino , Ratones , Envejecimiento , Metabolismo , Enfermedad de Alzheimer , Metabolismo , Medicamentos Herbarios Chinos , Farmacología , Proteína HMGB1 , Genética , Metabolismo , Hipocampo , Metabolismo , Peptidilprolil Isomerasa de Interacción con NIMA , Isomerasa de Peptidilprolil , Genética , Metabolismo , ARN Mensajero , Genética , Metabolismo
8.
Acta Pharmaceutica Sinica ; (12): 264-269, 2009.
Artículo en Chino | WPRIM | ID: wpr-278272

RESUMEN

Malignant tumor, one of the most refractory diseases, plays a threaten role in human health, the therapy and research on malignant tumor have taken a long way to go. The anti-tumor drugs which are the essential therapy strategies upgrade with the development of new anti-tumor targets and the research on tumor pathogenesis. Aurora kinase and Pin1, the novel anti-tumor targets, maintain the important relationship with tumor. Many new compounds designed on these targets have excellent anti-tumor effects and also enter into phase I or phase II clinical trial.


Asunto(s)
Humanos , Antineoplásicos , Farmacología , Apoptosis , Aurora Quinasas , Peptidilprolil Isomerasa de Interacción con NIMA , Naftoquinonas , Farmacología , Neoplasias , Metabolismo , Patología , Isomerasa de Peptidilprolil , Metabolismo , Piperazinas , Farmacología , Proteínas Serina-Treonina Quinasas , Metabolismo
9.
Journal of Central South University(Medical Sciences) ; (12): 1132-1136, 2008.
Artículo en Chino | WPRIM | ID: wpr-814138

RESUMEN

OBJECTIVE@#To detect the expression of peptidylprolyl cis/trans isomerase NIMA-interacting l (pin1 mRNA) in the circulation of non-small cell lung cancer (NSCLC) and to investigate the effect of ligating pulmonary vein first or ligating pulmonary artery first during operation on haematogenous dissemination of cancer cells.@*METHODS@#Twenty-six consecutive patients with NSCLC who underwent surgical resection with curative intention were randomly assigned into pulmonary artery first-ligation group (PA group) and pulmonary vein first-ligation group (PV group). Blood samples were collected just before and 7 days after the operation. During the lobectomy, blood samples of the proximal part and distal part of the pulmonary vein when it was ligated were collected. Another 10 patients with benign lung disease served as control subjects undergoing surgical resection, and 10 healthy persons served as negative controls. All blood samples were subjected to real-time RT-PCR with pin1 mRNA as the marker.@*RESULTS@#Compared with the benign lung disease and healthy persons, pin1 mRNA in NSCLC was overexpressed (1.45 to approximately 29.86 vs.0.83 to approximately 1.26 vs 1, P0.05; 16.84+/-2.36 vs.13.36+/-1.78, P>0.05).@*CONCLUSION@#pin1 mRNA was overexpressed in the circulation of NSCLC. Ligation of pulmonary vein before the ligation of the pulmonary artery may decrease the expression of pin1 mRNA in the circulation, which can prevent the release of tumor cells into the bloodstream.


Asunto(s)
Femenino , Humanos , Masculino , Carcinoma de Pulmón de Células no Pequeñas , Sangre , Cirugía General , Ligadura , Métodos , Neoplasias Pulmonares , Sangre , Cirugía General , Peptidilprolil Isomerasa de Interacción con NIMA , Isomerasa de Peptidilprolil , Genética , Metabolismo , Arteria Pulmonar , Cirugía General , Procedimientos Quirúrgicos Pulmonares , Métodos , Venas Pulmonares , Cirugía General , ARN Mensajero , Genética , Metabolismo
10.
Acta Pharmaceutica Sinica ; (12): 9-17, 2008.
Artículo en Chino | WPRIM | ID: wpr-268180

RESUMEN

Pin1 is a phosphorylation-dependent peptidyl-prolyl cis/trans isomerase, which specifically catalyzes the amide bond isomerization of phosphoserine-proline or phosphothreonine-proline in mitotic phosphoproteins. Pin1 induces the conformational changes to control the function of phosphoproteins. Depletion of Pinl on various human cancer cell lines cause mitotic arrest and apoptosis. Pin1 is an attracting therapeutic target for anticancer and its inhibitors might be potential anticancer drug. In this review, Pin1 inhibitors and the catalytic mechanism, the biological function of Pin1 and its role in oncogenesis are summarized.


Asunto(s)
Humanos , Apoptosis , Inhibidores Enzimáticos , Farmacología , Mitosis , Peptidilprolil Isomerasa de Interacción con NIMA , Neoplasias , Isomerasa de Peptidilprolil , Metabolismo , Fosfoproteínas , Química , Metabolismo , Fosforilación , Transducción de Señal
11.
Mycobiology ; : 209-213, 2006.
Artículo en Inglés | WPRIM | ID: wpr-729374

RESUMEN

Agrocybe cylindracea, an edible mushroom belonging to Bolbitiaceae, Agaricales, is widely used as invaluable medicinal material in the oriental countries. This study was initiated to find the genes expressed during the fruiting body formation of A. cylindracea. The cDNAs expressed differentially during fruiting body morphogenesis of A. cylindracea were isolated through subtractive hybridization between vegetative mycelia and fruiting bodies. The cDNAs expressed in the fruiting body morphogenesis of A. cylindracea were cloned and twenty genes were identified. Eleven were homologous to genes of known functions, three were homologous to genes in other organism without any function known. Six were completely novel genes specific to A. cylindracea so far examined. Some genes with known functions were a pleurotolysin, a self-assembling poreforming cytolysins; Aa-Pri1 and Pir2p, specifically induced genes during fruiting initiation of other mushroom, Agrocybe aegerita; an amino acid permease; a cytochrome P450; a MADS-box gene; a peptidylprolyl isomerase; and a serine proteinase. For other clones, no clear function was annotated so far. We believe the first report of the differentially expressed genes in fruiting process of A. cylindracea will be great helps for further research.


Asunto(s)
Agaricales , Agrocybe , Sistemas de Transporte de Aminoácidos , Células Clonales , Sistema Enzimático del Citocromo P-450 , Citotoxinas , ADN Complementario , Frutas , Expresión Génica , Morfogénesis , Isomerasa de Peptidilprolil , Perforina , Serina Proteasas
12.
Chinese Journal of Stomatology ; (12): 623-626, 2006.
Artículo en Chino | WPRIM | ID: wpr-293029

RESUMEN

<p><b>OBJECTIVE</b>To investigate the expression of Pin1, beta-catenin and cyclin D1 in salivary adenoid cystic carcinomas (SACC) and to evaluate the role of beta-catenin and Pin1 in SACC carcinogenesis.</p><p><b>METHODS</b>The expressions of Pin1, beta-catenin and cyclin D1 were examined in the specimens of 65 patients with SACC by immunohistochemistry, and Pin1 protein and mRNA expressions detected by Western blot and RT-PCR in four SACC cell lines.</p><p><b>RESULTS</b>Pin1 was overexpressed in 51 cases of ACC (78%), and 41 (63%) cases showed positive immunoreactivity for cyclin D1 protein in the nuclear fraction in tumor tissues. Fourteen (22%) cases showed positive immunoreactivity for beta-catenin protein in the nuclear/cytoplasmic fraction in tumor tissues, 6 of which exhibited quite evident expression of beta-catenin in nucleolus. The expression of membranous beta-catenin was down-regulated in most of the patients with lymph node metastasis (11/14).</p><p><b>CONCLUSIONS</b>The results suggest that Pin1 and beta-catenin signalling pathway were activated in SACC and might play a pivotal role in SACC carcinogenesis and metastasis.</p>


Asunto(s)
Humanos , Carcinoma Adenoide Quístico , Metabolismo , Patología , Línea Celular Tumoral , Ciclina D1 , Metabolismo , Metástasis Linfática , Peptidilprolil Isomerasa de Interacción con NIMA , Invasividad Neoplásica , Isomerasa de Peptidilprolil , Metabolismo , Neoplasias de las Glándulas Salivales , Metabolismo , Patología , beta Catenina , Metabolismo
13.
Journal of Huazhong University of Science and Technology (Medical Sciences) ; (6): 120-2, 2006.
Artículo en Inglés | WPRIM | ID: wpr-634312

RESUMEN

In order to investigate the expression levels of Pin1 mRNA and protein in cervical cancer and its association with Ki67 and their clinical significance, amplification of Pin1 gene was examined by RT-PCR, and the expression of both Pin1 and Ki67 protein was detected by immunohistochemistry in cervical cancer tissues. It was shown that the expression levels of Pin1 were higher in cervical cancer than in normal cervical tissues (P 0.05). The expression of Pin1 was significantly higher in adenocarcinoma than in squamous carcinoma of the uterine cervix (P < 0.05). In cervical cancer, the overexpression of Pin1 was positively correlated with that of Ki67 (P < 0.05). These results suggested that the overexpression of Pin1 was closely related with cancer cell proliferation or progression of cervical cancer and contributed to oncogenesis. Pin1 may serve as a potential marker for cervical cancer diagnosis.


Asunto(s)
Displasia del Cuello del Útero/metabolismo , Antígeno Ki-67/biosíntesis , Antígeno Ki-67/genética , Isomerasa de Peptidilprolil/biosíntesis , Isomerasa de Peptidilprolil/genética , Biomarcadores de Tumor , Neoplasias del Cuello Uterino/metabolismo
14.
Journal of Zhejiang University. Medical sciences ; (6): 500-514, 2004.
Artículo en Chino | WPRIM | ID: wpr-353273

RESUMEN

<p><b>OBJECTIVE</b>To study the expression of peptidyl-prolyl cis/trans isomerase (PPIase or Pin1) in malignant hematopoietic cells and its relation with cell cycle.</p><p><b>METHODS</b>Realtime quantitative PCR with fluorescence probe hybridization was used to measure expression of Pin1 mRNA in malignant hematopoietic cell lines and normal mononuclear cells separated from bone marrow. HeLa cells were blocked with Thymidine and Nocodazole in different cell phases and then the expression of Pin1 mRNA and protein were detected by realtime-PCR and immunoblotting.</p><p><b>RESULTS</b>The expression of Pin1 in malignant hematopoietic cell lines was significantly higher than that in normal controls (0.339 +/-0.093 compared with 0.038 +/-0.005, P<0.01). Its expression in myeloid malignant hematopoietic cell lines was significantly higher than that in normal controls (0.388 +/-0.115 compared with 0.038 +/-0.005, P<0.01) and so was the malignant lymphocytic cell lines (0.226 +/-0.166 compared with 0.038 +/-0.005, P<0.01). The expression of Pin1 was closely correlated with cell cycle. It was the highest in G1 phase and the lowest in S phase (110.762 +/-16.737 compared with 4.080 +/-0.634, P<0.01).</p><p><b>CONCLUSION</b>Pin1 is overexpressed in malignant hematopoietic cell lines and its expression is different during cell cycle that is highest in G1 phase and lowest in S phase.</p>


Asunto(s)
Humanos , Ciclo Celular , Fisiología , Fase G1 , Leucemia Linfoide , Patología , Leucemia Mieloide , Patología , Isomerasa de Peptidilprolil , Genética , ARN Mensajero , Genética , Fase S , Células Tumorales Cultivadas
15.
Dermatol. peru ; 13(2): 121-123, mayo-ago 2003. ilus, tab
Artículo en Español | LILACS, LIPECS | ID: lil-409649

RESUMEN

El modo de acción de inmunomodulares selectivos como las lactosas de los macrólidos: ciclosporina, tacrolimus, pimecrolimus, sirolimus, es a través de su unión a proteínas en el citoplasma, formando un complejo que inhibe la actividad de la enzima fosfatasa de calcineurina, en diferentes niveles, permitiendo por esta vía modificar la activación de las células t. Avances en la farmacocinética y farmacodinamia de estas drogas se está conociendo y por ende ampliando su espectro de acción.


Asunto(s)
Calcineurina , Adyuvantes Inmunológicos/uso terapéutico , Isomerasa de Peptidilprolil
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