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1.
BMC Bioinformatics ; 24(1): 202, 2023 May 17.
Artigo em Inglês | MEDLINE | ID: mdl-37193964

RESUMO

BACKGROUND: Finding drugs that can interact with a specific target to induce a desired therapeutic outcome is key deliverable in drug discovery for targeted treatment. Therefore, both identifying new drug-target links, as well as delineating the type of drug interaction, are important in drug repurposing studies. RESULTS: A computational drug repurposing approach was proposed to predict novel drug-target interactions (DTIs), as well as to predict the type of interaction induced. The methodology is based on mining a heterogeneous graph that integrates drug-drug and protein-protein similarity networks, together with verified drug-disease and protein-disease associations. In order to extract appropriate features, the three-layer heterogeneous graph was mapped to low dimensional vectors using node embedding principles. The DTI prediction problem was formulated as a multi-label, multi-class classification task, aiming to determine drug modes of action. DTIs were defined by concatenating pairs of drug and target vectors extracted from graph embedding, which were used as input to classification via gradient boosted trees, where a model is trained to predict the type of interaction. After validating the prediction ability of DT2Vec+, a comprehensive analysis of all unknown DTIs was conducted to predict the degree and type of interaction. Finally, the model was applied to propose potential approved drugs to target cancer-specific biomarkers. CONCLUSION: DT2Vec+ showed promising results in predicting type of DTI, which was achieved via integrating and mapping triplet drug-target-disease association graphs into low-dimensional dense vectors. To our knowledge, this is the first approach that addresses prediction between drugs and targets across six interaction types.


Assuntos
Descoberta de Drogas , Reposicionamento de Medicamentos , Descoberta de Drogas/métodos , Proteínas , Interações Medicamentosas , Conhecimento
2.
Br J Cancer ; 125(5): 748-758, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-34131308

RESUMO

BACKGROUND: Prognostic stratification of breast cancers remains a challenge to improve clinical decision making. We employ machine learning on breast cancer transcriptomics from multiple studies to link the expression of specific genes to histological grade and classify tumours into a more or less aggressive prognostic type. MATERIALS AND METHODS: Microarray data of 5031 untreated breast tumours spanning 33 published datasets and corresponding clinical data were integrated. A machine learning model based on gradient boosted trees was trained on histological grade-1 and grade-3 samples. The resulting predictive model (Cancer Grade Model, CGM) was applied on samples of grade-2 and unknown-grade (3029) for prognostic risk classification. RESULTS: A 70-gene signature for assessing clinical risk was identified and was shown to be 90% accurate when tested on known histological-grade samples. The predictive framework was validated through survival analysis and showed robust prognostic performance. CGM was cross-referenced with existing genomic tests and demonstrated the competitive predictive power of tumour risk. CONCLUSIONS: CGM is able to classify tumours into better-defined prognostic categories without employing information on tumour size, stage, or subgroups. The model offers means to improve prognosis and support the clinical decision and precision treatments, thereby potentially contributing to preventing underdiagnosis of high-risk tumours and minimising over-treatment of low-risk disease.


Assuntos
Biomarcadores Tumorais/genética , Neoplasias da Mama/patologia , Perfilação da Expressão Gênica/métodos , Neoplasias da Mama/genética , Bases de Dados Genéticas , Sistemas de Apoio a Decisões Clínicas , Feminino , Humanos , Aprendizado de Máquina , Gradação de Tumores , Análise de Sequência com Séries de Oligonucleotídeos , Prognóstico , Análise de Sobrevida
7.
Appl Opt ; 10(4): 913-5, 1971 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-20094561

RESUMO

One of the proposed storage media for semipermanent optical stores is an array of bleached holograms fabricated on photographic plates. If a store utilizing this medium is to be operated in a field environment, the effect of humidity variation requires consideration. In this study holograms were made using either Burckhardt's potassium ferricyanide or Russo and Sottini's modified R-10 type bleach on Kodak 649F and Agfa 10E70 plates. Diffraction efficiency was measured as a function of relative humidity over the range 30-98%. For holograms fabricated and tested as described above it was found that relative humidity values above 75% caused a permanent loss in diffraction efficiency for potassium ferricyanide bleached plates; humidity above 90% produced a temporary loss in R-10 bleached plates.

8.
Appl Opt ; 5(10): 1652-6, 1966 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-20057598

RESUMO

Carbon disulfide has identical microwave and optical dielectric constants, as well as extremely low optical and microwave loss. These properties make it possible to construct long travelingwave light modulators at microwave frequencies using the Kerr electrooptic effect induced in CS(2) by an electric field propagating on a TEM transmission line.Several experiments with traveling-wave Kerr cells consisting of resonant strip transmission lines immersed in CS(2) are described. A decrease in the microwave power required for modulation by a factor of two, by cooling the modulators to a temperature of -55 degrees C, is demonstrated. Simultaneous modulation of light at two microwave frequencies by excitation of two of the longitudinal modes of the strip line resonator is also described. Relatively high efficiency modulation with long devices of this type is also reported. In these experiments, the microwave power required for large depths of modulation is reduced by almost two orders of magnitude compared to previously reported CS(2) light modulators, and is within less than a factor of two of the calculated power for cells up to 44 cm in length. For longer cells, increasingly larger than predicted powers are required.

9.
J Am Med Womens Assoc ; 23(5): 469-70, 1968 May.
Artigo em Inglês | MEDLINE | ID: mdl-4231242
10.
12.
J Am Med Womens Assoc ; 23(8): 748-9, 1968 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-4247140
14.
J Am Med Womens Assoc ; 23(9): 835-6, 1968 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-4247150
15.
J Am Med Womens Assoc (1972) ; 29(1): 49-50, 1974 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-4361357
16.
J Am Med Womens Assoc ; 24(5): 389-92, 1969 May.
Artigo em Inglês | MEDLINE | ID: mdl-4239449
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