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1.
J Fish Biol ; 92(1): 274-280, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-29210079

RESUMO

In the current study activity and latency to explore, as well as the correlation of these traits, were examined in individually marked juvenile Gadus morhua at 7, 10 and 13° C. It was concluded that individual rank order of both traits was maintained across temperature but that the level of change differed between individuals.


Assuntos
Comportamento Animal , Gadus morhua/fisiologia , Temperatura , Animais , Cadeias de Markov , Método de Monte Carlo
2.
J Fish Biol ; 87(2): 480-6, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26104859

RESUMO

Trophic use by Atlantic cod Gadus morhua juveniles was examined early and late in the shift from pelagic to benthic habitats. Changes in the proportion of pelagic copepods, estimates of benthic prey indicated by isotope mixing models and stable-isotope values between sample periods suggested a gradual shift towards a benthic niche. Values of the trophic proxies, however, changed most markedly in the largest juvenile group, suggesting a more rapid trophic niche shift, and in turn competitive advantage, of larger juveniles.


Assuntos
Ecossistema , Gadus morhua/fisiologia , Animais , Tamanho Corporal , Isótopos de Carbono/análise , Cadeia Alimentar , Conteúdo Gastrointestinal , Modelos Lineares , Isótopos de Nitrogênio/análise
3.
Nat Genet ; 13(1): 117-9, 1996 May.
Artigo em Inglês | MEDLINE | ID: mdl-8673089

RESUMO

The BRCA2 gene on chromosome 13 has been shown to be associated with familial male and female breast cancer. Here we describe a study on BRCA2 in 21 Icelandic families, including 9 with male breast cancer. We have previously reported linkage to the BRCA2 region in an Icelandic male breast cancer family and subsequently found a strong indication of linkage to BRCA2 and the same BRCA2 haplotype in breast cancer cases from 15 additional families, indicating a common origin. We describe a five base-pair deletion in exon 9 of BRCA2 in an affected male from the male breast cancer family. The same mutation occurs in all the families with the shared BRCA2 haplotype indicating a founder effect. Among mutation carriers there are 12 males with breast cancer, which accounts for 40% of all males diagnosed with breast cancer in Iceland over the past 40 years. Three of them have no family history of breast cancer indicating that this mutation may have variable penetrance. The same BRCA2 mutation appears to be associated with different cancer phenotypes in this population including male and female breast cancer, prostate cancer, pancreas cancer and ovarian cancer.


Assuntos
Neoplasias da Mama Masculina/genética , Neoplasias da Mama/genética , Cromossomos Humanos Par 13 , Proteínas de Neoplasias/genética , Deleção de Sequência , Fatores de Transcrição/genética , Proteína BRCA2 , Composição de Bases , Neoplasias do Endométrio/genética , Éxons , Família , Feminino , Ligação Genética , Marcadores Genéticos , Haplótipos/genética , Humanos , Islândia , Masculino , Linhagem , Fenótipo , Reação em Cadeia da Polimerase
4.
J Fish Biol ; 82(6): 2141-6, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23731159

RESUMO

The response of age 0+ year juvenile Atlantic cod Gadus morhua to the presence of age 1+ and age 3+ year conspecifics was measured with and without cover available. Juveniles reacted by aggregating more closely and maintaining distance from older conspecifics in an experimental setting without cover but only to age 3+ year conspecifics when cover was available. The results indicate that prior residence of older juveniles can affect age 0+ year juveniles during benthic settlement and highlights the conservation value of structurally complex nursery habitats.


Assuntos
Comunicação Animal , Canibalismo , Ecossistema , Gadus morhua/fisiologia , Fatores Etários , Animais , Tamanho Corporal , Modelos Lineares , Dinâmica Populacional , Comportamento Social
5.
J Fish Biol ; 81(5): 1696-714, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23020569

RESUMO

Two pairs of sympatric three-spined stickleback Gasterosteus aculeatus morphs and two single morph populations inhabiting mud and lava or rocky benthic habitats in four Icelandic lakes were screened for parasites and genotyped for MHC class IIB diversity. Parasitic infection differed consistently between G. aculeatus from different benthic habitats. Gasterosteus aculeatus from the lava or rocky habitats were more heavily infected in all lakes. A parallel pattern was also found in individual MHC allelic variation with lava G. aculeatus morphs exhibiting lower levels of variation than the mud morphs. Evidence for selective divergence in MHC allele number is ambiguous but supported by two findings in addition to the parallel pattern observed. MHC allele diversity was not consistent with diversity reported at neutral markers (microsatellites) and in Þingvallavatn the most common number of alleles in each morph was associated with lower infection levels. In the Þingvallavatn lava morph, lower infection levels by the two most common parasites, Schistocephalus solidus and Diplostomum baeri, were associated with different MHC allele numbers.


Assuntos
Alelos , Infecções por Cestoides/veterinária , Doenças dos Peixes/genética , Genes MHC da Classe II/genética , Variação Genética , Smegmamorpha , Infecções por Trematódeos/veterinária , Animais , Cestoides/fisiologia , Doenças dos Peixes/epidemiologia , Doenças dos Peixes/parasitologia , Islândia/epidemiologia , Repetições de Microssatélites/genética , Carga Parasitária , Prevalência , Smegmamorpha/genética , Smegmamorpha/parasitologia , Trematódeos/fisiologia , Infecções por Trematódeos/epidemiologia , Infecções por Trematódeos/genética
6.
J Fish Biol ; 81(4): 1422-6, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22957880

RESUMO

Fourteen new microsatellite loci were developed and tested on Atlantic herring Clupea harengus with 39 individuals from Iceland and 49 individuals from Norway. The microsatellites, which contain di, tri and tetranucleotide repeats, are polymorphic (7-30 alleles), with observed heterozygosity ranging between 0·69 and 1·00 and expected heterozygosity between 0·55 and 0·97.


Assuntos
Peixes/genética , Variação Genética , Repetições de Microssatélites/genética , Animais , Dados de Sequência Molecular
7.
Heredity (Edinb) ; 106(3): 472-87, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21224880

RESUMO

The ecological theory of adaptive radiation predicts that the evolution of phenotypic diversity within species is generated by divergent natural selection arising from different environments and competition between species. Genetic connectivity among populations is likely also to have an important role in both the origin and maintenance of adaptive genetic diversity. Our goal was to evaluate the potential roles of genetic connectivity and natural selection in the maintenance of adaptive phenotypic differences among morphs of Arctic charr, Salvelinus alpinus, in Iceland. At a large spatial scale, we tested the predictive power of geographic structure and phenotypic variation for patterns of neutral genetic variation among populations throughout Iceland. At a smaller scale, we evaluated the genetic differentiation between two morphs in Lake Thingvallavatn relative to historically explicit, coalescent-based null models of the evolutionary history of these lineages. At the large spatial scale, populations are highly differentiated, but weakly structured, both geographically and with respect to patterns of phenotypic variation. At the intralacustrine scale, we observe modest genetic differentiation between two morphs, but this level of differentiation is nonetheless consistent with strong reproductive isolation throughout the Holocene. Rather than a result of the homogenizing effect of gene flow in a system at migration-drift equilibrium, the modest level of genetic differentiation could equally be a result of slow neutral divergence by drift in large populations. We conclude that contemporary and recent patterns of restricted gene flow have been highly conducive to the evolution and maintenance of adaptive genetic variation in Icelandic Arctic charr.


Assuntos
Adaptação Fisiológica , Evolução Molecular , Truta/genética , Adaptação Fisiológica/genética , Animais , Análise por Conglomerados , Feminino , Variação Genética , Genética Populacional , Islândia , Masculino , Repetições de Microssatélites , Tipagem Molecular , Seleção Genética
8.
Fam Cancer ; 18(2): 153-160, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30251169

RESUMO

A comprehensive pedigree, usually provided by the counselee and verified by medical records, is essential for risk assessment in cancer genetic counseling. Collecting the relevant information is time-consuming and sometimes impossible. We studied the use of electronically ascertained pedigrees (EGP). The study group comprised women (n = 1352) receiving HBOC genetic counseling between December 2006 and December 2016 at Landspitali in Iceland. EGP's were ascertained using information from the population-based Genealogy Database and Icelandic Cancer Registry. The likelihood of being positive for the Icelandic founder BRCA2 pathogenic variant NM_000059.3:c.767_771delCAAAT was calculated using the risk assessment program Boadicea. We used this unique data to estimate the optimal size of pedigrees, e.g., those that best balance the accuracy of risk assessment using Boadicea and cost of ascertainment. Sub-groups of randomly selected 104 positive and 105 negative women for the founder BRCA2 PV were formed and Receiver Operating Characteristics curves compared for efficiency of PV prediction with a Boadicea score. The optimal pedigree size included 3° relatives or up to five generations with an average no. of 53.8 individuals (range 9-220) (AUC 0.801). Adding 4° relatives did not improve the outcome. Pedigrees including 3° relatives are difficult and sometimes impossible to generate with conventional methods. Pedigrees ascertained with data from pre-existing genealogy databases and cancer registries can save effort and contain more information than traditional pedigrees. Genetic services should consider generating EGP's which requires access to an accurate genealogy database and cancer registry. Local data protection laws and regulations have to be addressed.


Assuntos
Neoplasias da Mama/genética , Bases de Dados Genéticas/estatística & dados numéricos , Aconselhamento Genético/métodos , Anamnese/métodos , Linhagem , Proteína BRCA2/genética , Neoplasias da Mama/epidemiologia , Feminino , Predisposição Genética para Doença , Humanos , Islândia/epidemiologia , Incidência , Sistema de Registros/estatística & dados numéricos
9.
Vet Immunol Immunopathol ; 126(3-4): 351-61, 2008 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-18775570

RESUMO

Allergic diseases occur in most mammals, although some species such as humans, dogs and horses seem to be more prone to develop allergies than others. In horses, insect bite hypersensitivity (IBH), an allergic dermatitis caused by bites of midges, and recurrent airway obstruction (RAO), a hyperreactivity to stable born dust and allergens, are the two most prevalent allergic diseases. Allergic diseases involve the interaction of three major factors: (i) genetic constitution, (ii) exposure to allergens, and (iii) a dysregulation of the immune response determined by (i) and (ii). However, other environmental factors such as infectious diseases, contact with endotoxin and degree of infestation with endoparasites have been shown to influence the prevalence of allergic diseases in humans. How these factors may impact upon allergic disease in the horse is unknown at this time. The 3rd workshop on Allergic Diseases of the Horse, with major sponsorship from the Havemeyer Foundation, was held in Hólar, Iceland, in June 2007 and focussed on immunological and genetic aspects of IBH and RAO. This particular venue was chosen because of the prevalence of IBH in exported Icelandic horses. The incidence of IBH is significantly different between Icelandic horses born in Europe or North America and those born in Iceland and exported as adults. Although the genetic factors and allergens are the same, exported adult horses show a greater incidence of IBH. This suggests that environmental or epigenetic factors may contribute to this response. This report summarizes the present state of knowledge and summarizes important issues discussed at the workshop.


Assuntos
Obstrução das Vias Respiratórias/veterinária , Predisposição Genética para Doença/genética , Doenças dos Cavalos/imunologia , Doenças dos Cavalos/patologia , Hipersensibilidade/veterinária , Mordeduras e Picadas de Insetos/veterinária , Obstrução das Vias Respiratórias/genética , Obstrução das Vias Respiratórias/imunologia , Animais , Doenças dos Cavalos/genética , Cavalos , Hipersensibilidade/genética , Hipersensibilidade/imunologia , Hipersensibilidade/patologia , Mordeduras e Picadas de Insetos/imunologia
10.
Acta Radiol ; 48(9): 948-55, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18080359

RESUMO

BACKGROUND: The Icelandic breast cancer screening program, initiated November 1987 in Reykjavik and covering the whole country from December 1989, comprises biennial invitation to mammography for women aged 40-69 years old. PURPOSE: To estimate the impact of mammography service screening in Iceland on deaths from breast cancer. MATERIAL AND METHODS: Cases were deaths from breast cancer from 1990 onwards in women aged 40 and over at diagnosis, during the period November 1987 to December 31, 2002. Age- and screening-area-matched, population-based controls were women who had also been invited to screening but were alive at the time their case died. RESULTS: Using conditional logistic regression on the data from 226 cases and 902 controls, the odds ratio for the risk of death from breast cancer in those attending at least one screen compared to those never screened was 0.59 (95% CI 0.41-0.84). After adjustment for healthy-volunteer bias and screening-opportunity bias, the odds ratio was 0.65 (95% CI 0.39-1.09). CONCLUSION: These results indicate a 35-40% reduction in breast cancer deaths by attending the Icelandic breast cancer screening program. These results are consistent with the overall evidence from other observational evaluations of mammography-based programs.


Assuntos
Neoplasias da Mama/mortalidade , Mamografia/estatística & dados numéricos , Programas de Rastreamento/estatística & dados numéricos , Programas Nacionais de Saúde , Adulto , Idoso , Viés , Estudos de Casos e Controles , Feminino , Humanos , Islândia/epidemiologia , Pessoa de Meia-Idade
11.
Int J Food Microbiol ; 111(2): 112-25, 2006 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-16889858

RESUMO

The proliferation of specific spoilage organisms (SSO) and quality changes were evaluated in haddock fillets stored in styrofoam boxes at 0, 7 and 15 degrees C and under temperature fluctuations. A rapid electronic nose technique was used to monitor different classes of compounds, representing microbial metabolites that were characteristic for the onset of spoilage odors. Photobacterium phosphoreum predominated among the spoilage bacteria and high levels of TVB-N were observed at sensory rejection. Pseudomonas spp. appeared to be responsible for the development of sweet, fruity spoilage odors in haddock fillets coinciding with increasing response of the electronic nose CO sensor. H(2)S-producing bacteria, most likely Shewanella putrefaciens, were associated with the H(2)S sensor's response at abusive temperature conditions. Partial Least Squares Regression (PLSR) was used as an explorative tool to provide a better understanding of the spoilage potential of SSOs, by evaluating models based on electronic nose responses and counts of specific spoilage organisms to predict sensory quality (Torry scores). The best prediction of the sensory quality was obtained by PLSR models based on five variables: the electronic nose sensors (CO, NH(3) and H(2)S), pseudomonads counts and a time-temperature variable. Good agreement between the predicted and experimental data indicates that these variables characterize the sensory quality of haddock fillets stored under different temperatures.


Assuntos
Contaminação de Alimentos/análise , Conservação de Alimentos/métodos , Odorantes/análise , Alimentos Marinhos , Qualidade de Produtos para o Consumidor , Microbiologia de Alimentos , Análise Multivariada , Valor Preditivo dos Testes , Alimentos Marinhos/microbiologia , Alimentos Marinhos/normas , Temperatura , Fatores de Tempo
12.
J Clin Oncol ; 19(13): 3173-81, 2001 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-11432883

RESUMO

PURPOSE: To assess the risk of death in patients who survive more than 5 years after diagnosis of childhood cancer and to evaluate causes of death in fatal cases. PATIENTS AND METHODS: This was a population-based study in the five Nordic countries (Denmark, Finland, Iceland, Norway, and Sweden) using data of the nationwide cancer registries and the cause-of-death registries. The study cohort included 13,711 patients who were diagnosed with cancer before the age of 20 years between 1960 and 1989 and who survived at least 5 years from diagnosis. By December 31, 1995, 1,422 patients had died, and death certificates were assessed in 1,402. Standardized mortality ratios (SMRs) for validated causes of death were calculated based on 156,046 patient-years at risk. RESULTS: The overall SMR was 10.8 (95% confidence interval [CI], 10.3 to 11.5), mainly due to high excess mortality from the primary cancer. SMR for second cancer was 4.9 (95% CI, 3.9 to 5.9) and was 3.1 (95% CI, 2.8 to 3.5) for noncancer death. The pattern of causes of death varied markedly between different groups of primary cancer diagnoses and was highly dependent on time passed since diagnosis. Overall late mortality was significantly lower in patients treated during the most recent period of time, 1980 to 1989, compared with those treated from 1960 to 1979 (hazard ratio, 0.61; 95% CI, 0.54 to 0.70), and there was no increase in rates of death due to cancer treatment. CONCLUSION: Long-term survivors of childhood cancer had an increased mortality rate, mainly dying from primary cancers. However, modern treatments have reduced late cancer mortality without increasing the rate of therapy-related deaths.


Assuntos
Neoplasias/mortalidade , Adolescente , Adulto , Idade de Início , Causas de Morte , Criança , Pré-Escolar , Estudos de Coortes , Feminino , Finlândia/epidemiologia , Humanos , Islândia/epidemiologia , Lactente , Recém-Nascido , Masculino , Neoplasias/complicações , Neoplasias/terapia , Modelos de Riscos Proporcionais , Risco , Países Escandinavos e Nórdicos/epidemiologia , Análise de Sobrevida , Fatores de Tempo
13.
J Med Genet ; 39(7): 457-62, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12114473

RESUMO

OBJECTIVE: To estimate the risk of malignant diseases in families of probands with the same mutation in the BRCA2 gene. DESIGN: A cohort study using record linkage of a breast cancer family resource and the Icelandic Cancer Registry. SETTING: Iceland. SUBJECTS: Families of 995 breast cancer patients, from which 887 were tested for a single founder 999del5 mutation; 90 had the mutation and 797 did not. RESULTS: Relatives of probands with the mutation had significantly increased relative risk (RR) of breast cancer. For first degree relatives, the RR was 7.55 (95% CI 6.04 to 9.03) but was 1.72 (95% CI 1.49 to 1.96) in first degree relatives of probands without the mutation. For prostate and ovarian cancer, the first and second degree relatives of probands with the mutation had a significantly increased RR, but in families of probands without the mutation no significant familial risk was found. CONCLUSIONS: The 999del5 mutation in the BRCA2 gene explains a substantial proportion of familial risk of breast cancer in Iceland, but significant familial risk remains in relatives of probands without the mutation. For prostate and ovarian cancer, the mutation accounts for most of the familiality observed in families of breast cancer patients.


Assuntos
Genes BRCA2 , Mutação/genética , Neoplasias/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Neoplasias da Mama/epidemiologia , Neoplasias da Mama/genética , Neoplasias da Mama Masculina/epidemiologia , Neoplasias da Mama Masculina/genética , Estudos de Coortes , Feminino , Efeito Fundador , Ligação Genética/genética , Humanos , Islândia , Neoplasias Renais/epidemiologia , Neoplasias Renais/genética , Masculino , Pessoa de Meia-Idade , Neoplasias/epidemiologia , Neoplasias Ovarianas/epidemiologia , Neoplasias Ovarianas/genética , Neoplasias Pancreáticas/epidemiologia , Neoplasias Pancreáticas/genética , Neoplasias da Próstata/epidemiologia , Neoplasias da Próstata/genética , Fatores de Risco , Neoplasias Gástricas/epidemiologia , Neoplasias Gástricas/genética
14.
APMIS ; 102(9): 711-5, 1994 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7946275

RESUMO

Gastric carcinomas in 382 patients were studied histologically and the results from the preoperative endoscopic biopsies were compared with those from the resected specimens. Using the Laurén classification an overall histological diagnostic agreement between the two specimens was reached in 317 cases, or 83%. The highest diagnostic agreement, 87%, was for intestinal carcinomas. For diffuse carcinomas the diagnostic agreement was 75%. The disagreement in intestinal carcinomas was mainly due to foci of undifferentiated cells and/or signet-ring cells predominating in the biopsy. The disagreement in diffuse carcinomas was mainly because glandular structures were present at the surface in some of the cases and therefore led to an erroneous diagnosis of intestinal carcinoma. In conclusion, the intestinal type of gastric carcinoma can in most cases be diagnosed correctly from an endoscopic biopsy, whereas the diagnosis of a diffuse carcinoma is less accurate until the resected specimen is available for histological study.


Assuntos
Adenocarcinoma/patologia , Neoplasias Gástricas/patologia , Biópsia , Diagnóstico Diferencial , Gastroscopia , Humanos , Estudos Retrospectivos
15.
APMIS ; 96(3): 229-38, 1988 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-3348912

RESUMO

The Icelandic Cancer Registry has records of 1,720 cases of malignant tumours of the female breast diagnosed in 1,659 patients in the 30-year period 1955-1984. Of these, 1,658 tumours were invasive. Sufficient histological material existed for 1,666 malignant tumours to make it possible to classify them according to the criteria published by the WHO. The most frequent histological type was Ductal carcinoma: 1,064 neoplasms, or 64%. Second in frequency was Lobular carcinoma: 175 neoplasms, or 10%; third was Mucinous carcinoma: 115 neoplasms, or 7%; and fourth in frequency was Medullary carcinoma: 69 neoplasms, or 4%. The incidence of carcinoma of the breast increased by 74% from 37.0 per 100,000 per annum in 1955-59 to 64.4 per 100,000 in 1980-84. This increase in incidence affected all morphological types, but Lobular and Mucinous more than Ductal and Medullary. The survival times have improved with time. Unilateral tumours were 710 in the right and 837 in the left breast. Both breasts were involved 167 times (106 patients), and in 6 patients the side was not recorded. A second primary was more likely to develop when the first one was in the right breast. This study of malignant tumours of the breast is the tenth in a series of investigations into histological classification of tumours occurring in Iceland.


Assuntos
Neoplasias da Mama/epidemiologia , Carcinoma/epidemiologia , Fatores Etários , Neoplasias da Mama/classificação , Neoplasias da Mama/diagnóstico , Neoplasias da Mama/patologia , Carcinoma/classificação , Carcinoma/diagnóstico , Carcinoma/patologia , Feminino , Humanos , Islândia , Prognóstico
16.
APMIS ; 100(10): 930-41, 1992 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-1445699

RESUMO

Iceland is one of the high-risk countries for stomach cancer. During the period 1955-84 the incidence declined from 76 to 28 per 10(5) p.a. for males and from 30 to 12 for females. Tissue material from the primary site in 978 males and 448 females was available for histological typing. By the WHO classification tubular carcinoma was most frequent in both sexes, 66% in males and 63% in females, and signet-ring carcinoma second, 13% in males and 16% in females. By the Laurén classification in males 78.1% were intestinal and 16.5% diffuse carcinomas, and in females 73.1% were intestinal and 20.7% diffuse carcinomas. The decline in stomach cancer in Icelanders has mostly affected the intestinal type of tumour (Laurén) and the tubular type of tumour (WHO). Diffuse type tumours (Laurén) have declined slightly. This supports the theory that intestinal carcinomas are more influenced by environmental and especially dietary factors, and that diffuse carcinomas are more influenced by other as yet unknown factors. For epidemiological studies both histological classifications have their value, the WHO especially in that it is based on standard histopathological criteria and the Laurén especially in that it only includes two tumour types. The WHO classification can roughly be transcribed to the Laurén classification as tubular, mucinous and papillary carcinomas fall into the group of intestinal tumours, and signet-ring and more than half of undifferentiated carcinomas into the group of diffuse tumours.


Assuntos
Neoplasias Gástricas/epidemiologia , Adolescente , Adulto , Fatores Etários , Idoso , Criança , Pré-Escolar , Feminino , Humanos , Islândia/epidemiologia , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Fatores Sexuais , Neoplasias Gástricas/classificação , Neoplasias Gástricas/etiologia , Fatores de Tempo , Organização Mundial da Saúde
17.
Oncol Rep ; 6(1): 117-22, 1999.
Artigo em Inglês | MEDLINE | ID: mdl-9864413

RESUMO

Replication errors (RER) at microsatellite repeats indicate genomic instability in hereditary nonpolyposis colorectal cancer (HNPCC) and in some sporadic cancers. We have studied genomic instability in 313 sporadic breast tumors and in 106 tumors from BRCA2, 999del5 carriers at 43 genomic loci on 13 chromosomes. RER was observed in 8/419 (1.9%) of the cases at one or more chromosomal loci. The frequencies of type I and type II RER were similar. The majority of RER+ tumors showed ER+, PgR+, high S-phase fraction, tumor size >2 cm and LOH at 2p, 2q and 3p. All 8 RER+ tumors were of the ductal histotype. The breast cancer cases with RER are not part of an HNPCC syndrome and a family history of colorectal cancer growth is not detected in relatives, with the exception of one case. However, four of the RER+ cases are from individuals carrying the BRCA2, 999del5 mutation. We conclude that RER is a rare somatic event during human breast carcinogenesis and may be associated with progression of breast carcinomas.


Assuntos
Neoplasias da Mama/genética , Replicação do DNA , Repetições de Microssatélites , Proteínas de Neoplasias/genética , Fatores de Transcrição/genética , Adulto , Idade de Início , Idoso , Idoso de 80 Anos ou mais , Aneuploidia , Proteína BRCA2 , Neoplasias da Mama/epidemiologia , Neoplasias da Mama/patologia , Carcinoma Ductal de Mama/genética , Carcinoma Ductal de Mama/patologia , Cromossomos Humanos/genética , Cromossomos Humanos/ultraestrutura , DNA de Neoplasias/genética , Estrogênios , Saúde da Família , Feminino , Heterozigoto , Humanos , Islândia/epidemiologia , Perda de Heterozigosidade , Masculino , Pessoa de Meia-Idade , Neoplasias/epidemiologia , Neoplasias/genética , Neoplasias Hormônio-Dependentes/genética , Neoplasias Hormônio-Dependentes/patologia , Reação em Cadeia da Polimerase , Progesterona , Deleção de Sequência
18.
Pathol Res Pract ; 186(1): 92-4, 1990 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-2315217

RESUMO

Many studies have shown that unilateral breast cancer is more frequent in the left breast than in the right. This has been investigated in the Icelandic Cancer Registry. Information on all but 18 female breast cancer cases diagnosed in the forty-year-period from 1948 to 1987, a total of 2139 cases, was used. Of these 2011 were unilateral, 1069 were in the left breast, an excess of 13%. Primary breast cancer in both breasts was diagnosed in 81 women, 35 in the left breast first, and 46 in the right breast first. The excess risk of developing cancer remains for the left breast also for women who have already lost one breast because of cancer. Information on whether their relatives had developed breast cancer existed for 1197 of these women. Patients with an affected first degree relative were of 2.54 fold risk of developing contralateral primary breast cancer, but women with no affected relative were at a reduced risk (not significant). Patients with right sided breast cancer are more likely to have a relative with breast cancer. The breast cancer status of the relatives did not influence the risk of death, so a better survival of familial cases could not be shown.


Assuntos
Neoplasias da Mama/patologia , Neoplasias da Mama/epidemiologia , Família , Feminino , Humanos , Islândia/epidemiologia , Razão de Chances , Sistema de Registros
19.
J Agric Food Chem ; 48(6): 2353-9, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10888549

RESUMO

An electronic nose was used as a rapid technique to monitor changes in the headspace gas above capelin (Mallotus villosus) during storage at 0 and 5 degrees C. At both temperatures, refrigeration was compared with an ice/seawater cooling system. At 5 degrees C, the effect of added 0.2% acetic acid was also tested. Electronic nose measurements were compared to measurements of total volatile bases (TVB), gas chromatography of volatile compounds, and sensory analysis. TVB analysis indicated less spoilage in seawater/ice systems than in refrigeration, but the other measurements indicated more spoilage in the seawater system compared to refrigeration. The possibility of using only a few sensors in the electronic nose to predict TVB was studied using partial least squares regression and a saturated generalized linear model. The results reported herein indicate that rapid electronic nose measurements, which require no sample preparation, can be used to predict the TVB value of the raw material stored under different conditions.


Assuntos
Produtos Pesqueiros , Odorantes , Plantas Medicinais/química , Compostos de Enxofre/análise , Cromatografia Gasosa/métodos , Eletrônica , Conservação de Alimentos/métodos , Temperatura
20.
BMJ ; 305(6858): 855-7, 1992 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-1422397

RESUMO

OBJECTIVE: To investigate the risk of prostate, ovarian, and endometrial cancer among relatives of patients with breast cancer. DESIGN: Cohort study of 947 pedigrees in which the proband had breast cancer, linked with the Icelandic cancer registry. SETTING: Iceland. SUBJECTS: The 947 pedigrees included 29,725 people, of whom 1539 had breast cancer, 467 had prostate cancer, 135 ovarian cancer, and 105 endometrial cancer. MAIN OUTCOME MEASURES: Risk of prostate, ovarian, and endometrial cancer among blood relatives of women with breast cancer compared with risk in spouses. RESULTS: The risk of prostate cancer was significantly raised for all relatives (1.5), first degree relatives (1.4), and second degree relatives (1.3) of women with breast cancer. Risk of ovarian cancer was raised for all relatives (1.9) and first degree relatives (1.9) and risk of endometrial cancer was raised for all relatives only (1.9). The risk of prostate cancer was raised if the proband with breast cancer had a first degree relative with prostate cancer. CONCLUSIONS: Coaggregation exists between breast cancer and cancers of the prostate, ovaries, and endometrium. This risk relation is probably based on genes which act by increasing the risk for cancer at these sites. Environmental factors that are common among relatives may also play a part. Continued research is required into pathophysiological mechanisms that could explain these observations.


Assuntos
Neoplasias da Mama/genética , Neoplasias do Endométrio/genética , Neoplasias Ovarianas/genética , Neoplasias da Próstata/genética , Idoso , Idoso de 80 Anos ou mais , Neoplasias da Mama/epidemiologia , Estudos de Coortes , Neoplasias do Endométrio/epidemiologia , Feminino , Humanos , Islândia/epidemiologia , Masculino , Pessoa de Meia-Idade , Neoplasias Ovarianas/epidemiologia , Neoplasias da Próstata/epidemiologia , Fatores de Risco
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