Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 28
Filtrar
1.
Oncogene ; 8(10): 2653-8, 1993 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-8378077

RESUMEN

Mutations of the p53 tumour-suppressor gene are considered to be rare in human colorectal adenomas, a premalignant state of the digestive tract. We have analysed a series of 32 exophytic tumours of the colon and rectum for the presence of p53 protein. In 26 of the 28 pure adenomas, the presence of significant levels of p53 proteins was established by a sensitive two-point enzyme-linked immunosorbent assay. The detectability of p53 protein was frequently limited to PAb 1801, recognizing an N-terminal epitope. Immunoblotting of the fractions captured by the monoclonal antibodies revealed that PAb 421 reacted exclusively with a 53-kDa species, whereas an additional 48-kDa band was detected after incubation with PAb 1801. In the adenomas, the mutant conformation-specific PAb 240 was always negative and no mutations were detected on exons 5-8 in three large and highly dysplastic lesions, selected for their high p53 protein content. The remaining four of the 32 tumours presented foci of cancer. Three of these were shown to contain 'mutant' PAb 240-reactive p53, and gene mutations were identified in two by denaturing gradient gel electrophoresis and sequencing of the amplified products. Intense p53 nuclear immunohistochemical staining was associated with the malignant areas. We conclude that a novel mechanism affecting the regulation of p53 protein could occur in colorectal adenomas.


Asunto(s)
Adenoma/química , Neoplasias Colorrectales/química , Proteína p53 Supresora de Tumor/análisis , Anticuerpos Monoclonales , Secuencia de Bases , Neoplasias de la Mama/química , Genes p53/genética , Células HeLa , Humanos , Datos de Secuencia Molecular , Mutación/genética , Células Tumorales Cultivadas
2.
Genes Genet Syst ; 75(6): 335-42, 2000 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11280008

RESUMEN

The phylogenetic trees have been constructed for the mitochondrial ND5 gene sequences from the Japanese Leptocarabus ground beetles, which contain 101 specimens collected from nearly the complete distribution ranges of them consisting of five morphological species, i.e., Leptocarabus procerulus, L. kumagaii, L. hiurai, L. kyushuensis and L. arboreus. On the trees, there are recognized two major lineages, each of which is further divided into two or more sublineages. The phylogenetic lines are geographically linked. Two or more species occur in a single lineage, and the same species appear in different lines. We suggest that transformation from one type of morphology to another took place in parallel in various periods of evolution of the Japanese Leptocarabus. From the phylogenetic tree and the dating from the nucleotide substitution rate and the geohistorical data it is inferred that the ancestry of all the Japanese Leptocarabus species was derived from a protoform of L. kyushuensis inhabited the ancient Japan area, followed by separation into two lineages after split of the Japanese Islands from the Eurasian Continent. They then propagated distribution to occupy their own habitat ranges, during which the morphological transformation took place in some lineages.


Asunto(s)
Escarabajos/genética , ADN Mitocondrial/genética , Complejo IV de Transporte de Electrones/genética , Geografía , Mitocondrias/enzimología , NADH Deshidrogenasa/genética , Filogenia , Animales , ADN Ribosómico/genética , Bases de Datos Factuales , Ambiente , Evolución Molecular , Japón , Mitocondrias/genética , Fenotipo , ARN Ribosómico 28S/genética , Trehalasa/genética
3.
J Exp Clin Cancer Res ; 17(4): 491-6, 1998 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-10089073

RESUMEN

To study the altered mechanisms of cell cycle regulation in esophageal cancer, the expressions of cyclins involved in G1/S transition were analyzed in a series of 26 human esophageal cancer cell lines. To evaluate and compare the levels of cyclin expression, flow cytometric analysis was performed using human lymphocytes as control. Increased expressions of cyclin A, D1, D3 and E were found in 23.1% (6/26), 65.4% (17/26), 15.4% (4/26) and 57.7% (15/26) of the cell lines, respectively. All cell lines studied expressed less cyclin D2 than lymphocytes and the majority of the cell lines expressed cyclin D3 at levels similar to those of lymphocytes. Five cell lines expressed exceptionally high levels of cyclin E. Expressions of cyclin D1 and E were significantly elevated as compared to those of cyclin A, D2 and D3. These results suggest that increased expressions of the positive cell cycle regulators cyclin D1 and E may play an important role in esophageal carcinogenesis.


Asunto(s)
Ciclinas/análisis , Neoplasias Esofágicas/química , Biomarcadores de Tumor/análisis , Biomarcadores de Tumor/metabolismo , Ciclo Celular/fisiología , Ciclinas/metabolismo , Neoplasias Esofágicas/metabolismo , Citometría de Flujo , Humanos , Células Tumorales Cultivadas
4.
J Exp Clin Cancer Res ; 21(4): 547-53, 2002 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-12636101

RESUMEN

Peritoneal dissemination is the most frequent type of recurrence in patients with gastric cancer with serosal exposure, irrespective of whether they have undergone curative gastrectomy. The purpose of this study was to establish a method to detect micrometastatic cells in the abdominal cavity and predict peritoneal recurrence in patients with such gastric carcinomas. A total of 86 patients with gastric carcinoma, undergoing gastrectomy, were examined. Reverse transcriptase-polymerase chain reaction (RT-PCR) assay was used to detect carcinoembryonic antigen (CEA) mRNA in abdominal lavage fluid. Twenty-four cases without serosal exposure were negative, while all 13 cases with macroscopic peritoneal dissemination were positive for CEA mRNA. Among the 49 cases with macroscopic serosal invasion and without peritoneal metastasis, cancer cells were detected in 27 cases with RT-PCR while in only 6 cases with conventional cytology. All cytologically-positive cases were also positive for CEA mRNA. Among the 27 CEA-positive cases, 15 patients (56%) relapsed with peritoneal metastasis within 12 months after gastrectomy. In contrast, none of the 22 CEA-negative cases had peritoneal recurrence within 16-60 months of observation, whereas in 43 cytologically-negative cases, 10 patients relapsed with peritoneal recurrence. As compared with conventional cytological examination, this method would be clinically more beneficial for detecting free cancer cells in the peritoneal cavity and for predicting peritoneal recurrence in gastric carcinoma with serosal invasion.


Asunto(s)
Antígeno Carcinoembrionario/genética , Neoplasias Peritoneales/genética , ARN Mensajero/análisis , Neoplasias Gástricas/genética , Cavidad Abdominal , Secuencia de Bases , Cartilla de ADN , Femenino , Humanos , Masculino , Invasividad Neoplásica , Neoplasias Peritoneales/epidemiología , Neoplasias Peritoneales/mortalidad , Neoplasias Peritoneales/patología , Reacción en Cadena de la Polimerasa/métodos , Valor Predictivo de las Pruebas , ARN Mensajero/genética , Recurrencia , Valores de Referencia , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Sensibilidad y Especificidad , Neoplasias Gástricas/mortalidad , Neoplasias Gástricas/patología , Análisis de Supervivencia , Factores de Tiempo , Células Tumorales Cultivadas
5.
Hepatogastroenterology ; 45(24): 2117-22, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9951876

RESUMEN

BACKGROUND/AIMS: In planning adjuvant treatment of colorectal cancer, it is of critical importance to optimize the treatment by identifying subsets of patients that will respond or not to chemotherapy. Thymidylate synthase (TS) and dihydropyrimidine dehydrogenase (DPD) are key enzymes involved in the biochemical functions of the antimetabolite 5-fluorouracil (5-FU). In searching for the factors determining the 5-FU sensitivity of colorectal cancer, TS and DPD were analyzed in relation to the inhibitory effect of 5-FU on cell proliferation in a series of human colorectal cancer cell lines. METHODOLOGY: TS and DPD protein expressions were quantified in 5 human colorectal cancer cell lines, using TS binding assay and Western blotting, respectively. Cellular growth inhibition was assessed by MTT assay after 48 hours of continuous exposure to 5-FU or cisplatin (CDDP). RESULTS: TS protein expression was detected in all but one of the cell lines studied and varied within a 17-fold range, while DPD protein expression was detectable in only one cell line (CaR1). CaR1, which expressed the highest level of DPD and no detectable TS, showed remarkable resistance to 5-FU. The other colorectal cancer cell lines with undetectable DPD expression were sensitive to 5-FU. There was no correlation between TS expression and 5-FU sensitivity. All of the cell lines studied showed similar sensitivity to CDDP. CONCLUSIONS: These data suggest that DPD, but not TS, expression predicts 5-FU sensitivity in colorectal cancer cell lines.


Asunto(s)
Antimetabolitos Antineoplásicos/farmacología , División Celular/efectos de los fármacos , Neoplasias Colorrectales/tratamiento farmacológico , Fluorouracilo/farmacología , Oxidorreductasas/genética , Timidilato Sintasa/genética , Células Tumorales Cultivadas/efectos de los fármacos , División Celular/genética , Neoplasias Colorrectales/genética , Dihidrouracilo Deshidrogenasa (NADP) , Resistencia a Antineoplásicos/genética , Regulación Enzimológica de la Expresión Génica/fisiología , Humanos , Pronóstico , Células Tumorales Cultivadas/enzimología , Ensayo de Tumor de Célula Madre
6.
Hepatogastroenterology ; 46(26): 1192-8, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10370690

RESUMEN

The patient was a 22 year-old male. Hereditary chronic pancreatitis was suspected as a diagnosis since his mother's uncle had been operated on for chronic pancreatitis 14 years previously at the age of 64 years and his mother had been operated on for chronic pancreatitis with calculi 5 years previously at the age of 40 years. Surgery was needed, since: 1) he had experienced abdominal pain for 8 years; 2) endoscopic retrograde cholangiopancreatography (ERCP) revealed a marked irregular dilatation in the main pancreatic duct and a marked irregular dilatation and protein plugs in the ductule of the tail of the pancreas; and, 3) pancreatic functional diagnostic (PFD) test examination showed a 75% decrease in exocrine function. If a surgical procedure had not been performed, the patient would likely have experienced calculi formation in the pancreas and a further decrease in exocrine function. Since the patient was very young and had many protein plugs in the dilated ductule of the tail of the pancreas, we decided to perform a spleen-preserving Puestow's procedure with removal of the tail of the pancreas. Clinical and pathological findings of hereditary pancreatitis are reviewed.


Asunto(s)
Pancreatitis/genética , Adulto , Enfermedad Crónica , Femenino , Humanos , Masculino , Persona de Mediana Edad , Páncreas/patología , Pancreatectomía , Pancreatitis/patología , Pancreatitis/cirugía , Linaje , Tomografía Computarizada por Rayos X
8.
Mol Ecol Resour ; 9(2): 610-2, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21564706

RESUMEN

Eleven polymorphic microsatellite markers were developed from a (CA)(n) -enrichment library of the whitegirdled goby (Pterogobius zonoleucus). Polymorphism at these loci ranged from 2 to 12 alleles, and observed and expected heterozygosities from 0.05 to 0.90 and from 0.05 and 0.86, respectively. All loci conformed to Hardy-Weinberg equilibrium, with no significant linkage disequilibrium between all locus pairs. Cross-species amplification tests were successful in P. elapoides, and most loci were polymorphic. These microsatellite markers will be useful in further population genetic studies of both species.

9.
Br J Cancer ; 84(1): 57-63, 2001 Jan 05.
Artículo en Inglés | MEDLINE | ID: mdl-11139314

RESUMEN

p53 antibodies have been found in the sera of patients with various types of cancer. The presence of these antibodies is generally associated with p53 accumulation in the tumour that is believed to trigger this humoral response. The recent discovery of 2 new members of the p53 family, p73 and p63, led us to study the specificity of this immune response towards the 3 proteins. Serum samples from 148 patients with various types of cancer were tested for antibodies against p73 and p63 using immunoprecipitation. 72 patients were previously shown to have p53 antibodies whereas 76 were negative. The control group consisted of 50 blood donors. p73 were detected in 22/148 (14.9%) of the cancer patients (11/72 in the group with p53-antibodies and 11/76 in the negative group). Only two sera from the control (4%) were positive. p63 antibodies were detected in only 4/148 (2.7%) of the cancer patients. Epitope mappings were performed and demonstrate that p73 antibodies are directed toward the central region of the p73 protein whereas p53 antibodies react predominantly toward the amino- and the carboxy-terminus of p53. Our results indicate that there is a specific immune response toward the p73 protein in cancer patients, a finding supported by an increasing number of publications describing p73 accumulation in tumoral cells.


Asunto(s)
Anticuerpos Antineoplásicos/análisis , Proteínas de Unión al ADN/inmunología , Proteínas de la Membrana , Neoplasias/inmunología , Proteínas Nucleares/inmunología , Transactivadores , Neoplasias de la Mama/sangre , Neoplasias de la Mama/inmunología , Estudios de Casos y Controles , Reacciones Cruzadas/inmunología , Mapeo Epitopo/métodos , Estudios de Seguimiento , Genes Supresores de Tumor , Neoplasias de Cabeza y Cuello/sangre , Neoplasias de Cabeza y Cuello/inmunología , Humanos , Neoplasias Pulmonares/sangre , Neoplasias Pulmonares/inmunología , Neoplasias/sangre , Fosfoproteínas/inmunología , Factores de Transcripción , Proteína Tumoral p73 , Proteína p53 Supresora de Tumor/inmunología , Proteínas Supresoras de Tumor
10.
Jpn J Clin Oncol ; 27(6): 423-6, 1997 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-9438007

RESUMEN

We report a case of primary gastric carcinoma with a macroscopic appearance indistinguishable from that of a submucosal tumor. A 48-year-old man visited our hospital with a chief complaint of epigastric discomfort. Endoscopic examination revealed a protruding lesion with a well defined margin on the anterior wall of the gastric antrum. Most of the tumor surface was covered with apparently normal gastric mucosa and a shallow recess with mild erosion was observed on the top. Abdominal ultrasonography showed a hypoechoic lesion with an irregular margin under the gastric mucosa. Laboratory examination revealed an elevated CA19-9 level of 106.9 U/ml. In spite of repeated bouling biopsies, no histological diagnosis could be obtained before surgery. However, gastrectomy with regional lymph node dissection was performed because of the high likelihood of gastric cancer, in view of the markedly elevated CA19-9 level and irregular tumor margin demonstrated by abdominal ultrasonography. The tumor was diagnosed histologically as papillo-tubular adenocarcinoma invasive to the serosa with marked vessel infiltration. No metastasis was found in the regional lymph nodes. Gastric cancer resembling submucosal tumor is rare and often difficult to diagnose. Careful estimation of the possibility of gastric cancer and the informed consent of the patient are critically important, in cases of suspected primary gastric cancer resembling submucosal tumor, in order to decide the form of treatment.


Asunto(s)
Adenocarcinoma Papilar/patología , Mucosa Gástrica/patología , Neoplasias Gástricas/patología , Antígeno CA-19-9/análisis , Diagnóstico Diferencial , Gastroscopía , Humanos , Masculino , Persona de Mediana Edad , Antro Pilórico
11.
Mol Biol Evol ; 15(8): 1026-39, 1998 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-9718730

RESUMEN

Genealogical trees have been constructed using mitochondrial ND5 gene sequences of 78 Damaster (s. str.) specimens from all over the Japanese Islands. Eight lineages (called races in this paper) have been recognized. The races are tightly linked to geography with sharp distribution boundaries between them. The races and their distribution ranges do not coincide with those of classical morphology. Based on the observed distribution of the mitochondrial DNA haplotypes and the geohistorical data, we propose a diversification scenario of Damaster.


Asunto(s)
Escarabajos/anatomía & histología , Escarabajos/genética , ADN Mitocondrial/genética , Evolución Molecular , Animales , Secuencia de Bases , Escarabajos/clasificación , Cartilla de ADN/genética , Genes de Insecto , Japón , Datos de Secuencia Molecular , NADH Deshidrogenasa/química , NADH Deshidrogenasa/genética , Filogenia , Conformación Proteica , Homología de Secuencia de Ácido Nucleico , Especificidad de la Especie
12.
Dig Dis Sci ; 43(2): 306-10, 1998 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-9512122

RESUMEN

Mutation of the adenomatous polyposis coli (APC) gene is frequently found in colorectal tumors from both familial adenomatous polyposis (FAP) and non-FAP patients. Analysis of APC mutation is time-consuming and costly due to the large size of the APC gene. As the majority of APC mutations result in the truncation of gene products, the detection of truncated APC proteins may be used as a screening method for APC mutations. The aim of this study is to establish a practical method of detecting truncated APC proteins for the screening of APC mutations. APC proteins in human colorectal cancer cell lines were analyzed by western blotting. Truncated APC proteins were expressed in all of the colorectal cancer cell lines studied. Two species of truncated APC proteins were expressed in two cell lines. Western blotting is a rapid, reliable screening method for APC mutations and provides information on both alleles.


Asunto(s)
Neoplasias Colorrectales/metabolismo , Genes APC/genética , Mutación , Anticuerpos Monoclonales , Western Blotting , Electroforesis en Gel de Poliacrilamida , Humanos , Immunoblotting , Peso Molecular , Células Tumorales Cultivadas
13.
Crit Rev Oncog ; 3(3): 257-82, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1616957

RESUMEN

Mutations on the TP53 tumor suppressor gene and allele loss on chromosome 17p, where this gene has been located, are among the most frequent alterations yet identified in human malignancies. The p53 protein is highly conserved through evolution and expressed in most normal tissues. Wild-type p53 has been shown to control normal cell proliferation possibly through transcriptional regulation. The wild-type TP53 gene can suppress cell transformation and neoplastic cell growth. In contrast, mutant TP53 has lost the tumor suppressing ability and, in most cases, has gained a transformation promoting ability. Many different TP53 mutations have common conformational and functional consequences on the p53 protein. However, all the TP53 mutants are not necessarily equivalent in terms of biological activity: some mutations confer a strong transforming ability, while others lead to truncated products with probably no biological function. Some mutants may exhibit a dominant behavior over wild-type TP53, others may be recessive. Point mutations of TP53 tend to occur on evolutionary conserved positions. However, the TP53 mutational spectrum differs among cancer types, and this fact may reflect different exogenous mutagens and endogenous factors contributing to human carcinogenesis. In defined types of malignancies, the tumors with TP53 alteration or tumors with allele loss on 17p are associated with more aggressive phenotypes than those without these alterations. For these malignancies, the monitoring of TP53 alteration should now be included in therapeutic trials. Germ line mutations on TP53 may also occur. Individuals with constitutional TP53 mutation have a predisposition to a wide variety of neoplasms. Further characterization of this predisposition will enable the definition of the best follow-up for these at-risk patients.


Asunto(s)
Proteína p53 Supresora de Tumor/fisiología , Animales , Transformación Celular Neoplásica , Genes de Retinoblastoma , Genes p53 , Humanos , Mutación , Neoplasias/genética , Pronóstico
14.
Jpn J Cancer Res ; 88(9): 855-60, 1997 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9369933

RESUMEN

To study the altered mechanisms of cell cycle regulation in colorectal cancer, the expressions of cyclins, cyclin-dependent kinases (CDKs), CDK inhibitors, p53 and retinoblastoma (Rb) protein were analyzed by western blotting in a series of human colorectal cancer cell lines. The colorectal cancer cell lines exhibited various expression patterns of cell cycle regulators, which may reflect differences in the biological characteristics of cancer cells and in the genetic backgrounds of carcinogenesis. A correlation was found between p53 gene alteration and p21 expression, suggesting that p53 gene mutation usually suppresses p21 expression, though p21 expression could be induced via both a p53-dependent and a p53-independent pathway in colorectal cancer. None of the cell lines studied expressed p16 protein, suggesting that inactivation of p16 may be a common alteration in colorectal cancer. Moreover, all the D-type cyclins, especially D2 and D3, were expressed at a high level in most of the cell lines. Loss of p16 expression and increased expression of D-type cyclins promote CDK-mediated Rb phosphorylation. All of the colorectal cancer cell lines studied herein expressed Rb protein, but the growth-suppressive properties of Rb may be inactivated by the loss of p16 expression and increased expressions of D-type cyclins. In view of the pivotal role of Rb in cell cycle regulation, loss of p16 expression and overexpression of D-type cyclins may be critical alterations in colorectal cancer.


Asunto(s)
Ciclo Celular/fisiología , Neoplasias del Colon/patología , Neoplasias Colorrectales/patología , Quinasas Ciclina-Dependientes/biosíntesis , Ciclinas/biosíntesis , Neoplasias del Colon/metabolismo , Neoplasias Colorrectales/metabolismo , Quinasas Ciclina-Dependientes/antagonistas & inhibidores , Inhibidores Enzimáticos/metabolismo , Neoplasias Esofágicas/metabolismo , Neoplasias Esofágicas/patología , Genes p53 , Humanos , Proteína de Retinoblastoma/biosíntesis , Células Tumorales Cultivadas , Proteína p53 Supresora de Tumor/biosíntesis
15.
J Mol Evol ; 50(6): 541-9, 2000 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10835484

RESUMEN

Phylogenetic analyses based on the mitochondrial ND5 gene comparisons and the geohistory of the Japanese Islands suggest that each Japanese species belonging to the subtribe Carabina has its own history for the establishment of its present habitat in the Japanese Islands. It can be roughly classified into two categories: (1) species which were derived from the ancestry that inhabited ancient Japan at the time of its split from the Eurasian Continent [ca. 15 million years ago (MYA)], followed by diversification within the Japanese Islands; and (2) species which invaded Hokkaido from the Eurasian Continent through land-bridges from Sakhalin and/or the Kuriles or from western Japan from the Korean Peninsula during the glacial era (<2 MYA).


Asunto(s)
Escarabajos/genética , ADN Mitocondrial/genética , NADH Deshidrogenasa/genética , Filogenia , Animales , Evolución Molecular , Japón , Datos de Secuencia Molecular , Análisis de Secuencia de ADN
16.
Cancer ; 75(5): 1061-4, 1995 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-7850702

RESUMEN

BACKGROUND: There has been considerable controversy with regard to surgical strategies for the treatment of superficial esophageal carcinoma, which is characterized by tumor confined within the epithelium (EP), muscularis mucosae (MM), or submucosa (SM). The relationships among macroscopic shape, depth of invasion, and lymph node involvement in superficial tumors were investigated to devise therapeutic strategies for patients with such disease. METHODS: Thirty-three patients with superficial primary esophageal cancer underwent esophagectomy with regional lymph node dissection (3 EP, 6 MM, and 24 SM). Tumors were divided into two types according to macroscopic characteristics: (1) tumors with elevated components and (2) flat or depressed tumors without an elevated component. RESULTS: Tumors with an elevated component (n = 19) showed invasion of the deep layer, and a high incidence of lymph node metastasis. Conversely, tumors without an elevated component (n = 14) showed varied depths of invasion, and, with one exception, had no lymph node involvement. CONCLUSIONS: The existence of an elevated component in superficial esophageal cancer is an important macroscopic feature suggesting submucosal invasion and a high probability of lymph node involvement. More intensive treatment should be adopted for such tumors, whereas localized resection may be feasible for tumors without an elevated component.


Asunto(s)
Neoplasias Esofágicas/patología , Neoplasias Esofágicas/cirugía , Esofagectomía , Esofagoscopía , Humanos , Incidencia , Escisión del Ganglio Linfático , Metástasis Linfática/patología , Invasividad Neoplásica/patología , Neoplasias de Tejido Vascular/patología
17.
J Orthop Sci ; 3(4): 221-4, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9662666

RESUMEN

We report a case of primary iliopsoas abscess successfully treated by ultrasonographically guided percutaneous drainage. A 56-year-old man presented at our hospital with lumbago, right-sided back pain, fever (temperature 38.5 degrees C) and chills. On physical examination, we found dark red skin, swelling, and tenderness localized at the right side at the back of his waist. Laboratory examination showed leukocytosis (white blood cell count 9700/mm3) with a leftward shift and elevated C-reactive protein (5.2 mg/dl). Ultrasonography (US), computed tomography (CT), and magnetic resonance imaging revealed a hypodense lesion in the right iliopsoas muscle extending to the subcutaneous tissue. About 50 ml of thick yellow pus was obtained by ultrasonographically guided aspiration drainage. A drain catheter was inserted in the abscess cavity. Laboratory findings improved and clinical symptoms abated rapidly after drainage. On the twenty-first day after drainage, US and CT showed that the abscess was no longer present. The patient was discharged after 32 days of hospitalization. As possible primary diseases causing iliopsoas abscess, such as digestive tract disease, tuberculosis, and osteomyelitis, were not found, we diagnosed the disease as primary iliopsoas abscess. Although surgical drainage has been performed in most reported cases of iliopsoas abscess, this case report shows that ultrasonographically guided percutaneous drainage is also effective for treating primary iliopsoas abscess if it is diagnosed early enough.


Asunto(s)
Drenaje/métodos , Absceso del Psoas/terapia , Ultrasonografía Intervencional , Proteína C-Reactiva/análisis , Drenaje/instrumentación , Estudios de Seguimiento , Humanos , Ilion , Leucocitosis/patología , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Absceso del Psoas/diagnóstico , Absceso del Psoas/diagnóstico por imagen , Tomografía Computarizada por Rayos X
18.
Adv Biophys ; 36: 65-106, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10463073

RESUMEN

The phylogenetic relationships of the carabid ground beetles have been estimated by analysing a large part of the ND5 gene sequences of more than 1,000 specimens consisting of the representative species and geographic races covering most of the genera and subgenera known in the world. From the phylogenetic analyses in conjunction with the mtDNA-based dating, a scenario of the establishment of the present habitats of the respective Japanese carabids has been constructed. The carabid diversification took place ca. 40 MYA as an explosive radiation of the major genera. During evolution, occasional small or single bangs also took place, sometimes accompanied by parallel morphological evolution in phylogenetically remote as well as close lineages. The existence of silent periods, in which few morphological changes took place, has been recognized during evolution. Thus, the carabid evolution is discontinuous, alternatively having a phase of rapid morphological change and a silent phase.


Asunto(s)
Evolución Biológica , Escarabajos/clasificación , Escarabajos/genética , ADN Mitocondrial/análisis , Animales , Escarabajos/fisiología , Evolución Molecular , Femenino , Variación Genética , Japón , Masculino , Filogenia , Reacción en Cadena de la Polimerasa , Especificidad de la Especie
19.
Surg Today ; 29(4): 385-8, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10211577

RESUMEN

We herein describe a 27-year-old male presenting with a pulmonary blastoma. The patient was admitted to our hospital with the chief complaints of fever and left back pain. Chest roentgenograms showed a tumor measuring 10 cm in diameter in a lower lobe of the left lung. Computed tomography and magnetic resonance imaging revealed a well demarcated and heterogeneously enhanced tumor. Although a histological diagnosis could not be obtained by a transbronchial biopsy, image analyses led us to suspect it to be malignant. The patient underwent a left lower lobectomy with lymph node dissection. A histopathological examination revealed the tumor to be a biphasic type of pulmonary blastoma. Because of the rapid progress of the tumor and the difficulty in making a preoperative diagnosis in such cases, an immediate surgical resection is therefore recommended in cases with even the slightest suspicion of malignancy.


Asunto(s)
Neoplasias Pulmonares/cirugía , Blastoma Pulmonar/cirugía , Adulto , Quimioterapia Adyuvante , Humanos , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/tratamiento farmacológico , Neoplasias Pulmonares/patología , Imagen por Resonancia Magnética , Masculino , Pronóstico , Blastoma Pulmonar/diagnóstico , Blastoma Pulmonar/tratamiento farmacológico , Blastoma Pulmonar/patología , Tomografía Computarizada por Rayos X
20.
Cytometry ; 31(1): 60-6, 1998 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-9450526

RESUMEN

Immunochemical methods were developed for the optimal detection and characterization of total cellular p53 protein expression, both in the nuclear-attached and soluble fractions of colorectal cancers, in order to improve the correlation between protein deregulation and gene status. Seventy colorectal carcinomas were studied using 3 monoclonal antibodies in a sensitive analyzing system combining flow cytometry (nuclear-bound fraction) and enzyme-linked immunosorbent assay (ELISA; soluble fraction). DNA indices were calculated on the DNA histograms and mutations of the p53 gene were searched for in a subset of 41 cases. Three p53 expression patterns were found: 35 tumors were classified as pattern "A," characterized by high p53 expression including "mutant" conformation and missense mutations of the gene (16/17 cases tested), pattern "B" consisted of 15 tumors with total absence of p53 expression corresponding to nonsense mutations of the gene (8/9 cases tested), and pattern "C" of 20 tumors presenting low or undetectable nuclear-bound p53 but intermediate p53 protein content (pAb (1801+) in the soluble fraction. The latter pattern was associated with wild-type genes (14/15 cases tested), and with tumors that were often localized in the right colon compared to pattern "A" and "B" tumors (45% versus 8%, P < 0.009) and were frequently near-diploid (80% versus 29%, P < 0.0002). No correlation was found between tumor stage and the patterns of p53 expression. The results indicate that both flow cytometry (FCM) and ELISA seem necessary for the proper characterization of the p53 expression pattern, thus achieving a high degree of concordance with molecular analysis of gene mutations.


Asunto(s)
Adenoma/química , Neoplasias Colorrectales/química , Proteínas de Neoplasias/análisis , Proteína p53 Supresora de Tumor/análisis , Ensayo de Inmunoadsorción Enzimática , Citometría de Flujo , Humanos , Mutación , Fenotipo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA