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1.
Pharmacogenomics ; 21(11): 751-759, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-32615909

RESUMEN

Background: Tumor-infiltrating lymphocytes (TILs) and postoperative chemotherapeutics interact in the tumor micro-environment. This interaction has not been well investigated in gastric cancer. Materials & methods: A total of 129 patients were divided into high or low TILs based on the median number of positive CD3+ and FoxP3+ T cells, which was assessed by immunocytochemistry. Results: Cox regression analysis showed that the stage III disease with shorter overall survival was significant. The analysis showed that high numbers of CD3+ or FoxP3+ T cells have better clinical outcomes in FOLFOX-treated patients. Conclusion: High CD3+ and FoxP3+ T-cell infiltration was associated with better clinical outcomes in patients with gastric cancer treated with FOLFOX, suggesting TILs incorporated into algorithms to improve the therapeutic efficacy of optimal chemotherapy.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/inmunología , Linfocitos Infiltrantes de Tumor/inmunología , Neoplasias Gástricas/tratamiento farmacológico , Neoplasias Gástricas/inmunología , Microambiente Tumoral/inmunología , Adulto , Biomarcadores de Tumor/inmunología , Femenino , Fluorouracilo/administración & dosificación , Fluorouracilo/inmunología , Humanos , Leucovorina/administración & dosificación , Leucovorina/inmunología , Masculino , Persona de Mediana Edad , Compuestos Organoplatinos/administración & dosificación , Compuestos Organoplatinos/inmunología , Estudios Retrospectivos , Neoplasias Gástricas/mortalidad , Tasa de Supervivencia/tendencias , Resultado del Tratamiento , Microambiente Tumoral/efectos de los fármacos
2.
Pharmacogenomics ; 19(14): 1111-1123, 2018 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-30136624

RESUMEN

AIM: Delayed recovery from general anesthesia is a well-known complication that requires predictive tools and approaches. This study aimed to determine significant factors associated with postanesthesia recovery and to develop an algorithm for estimating recovery time from general anesthesia. MATERIALS & METHODS: The genotypes of patients were determined by SNaPshot or ARMS-qPCR. The algorithm was developed via machine-learning and tested by the worm plot. RESULTS: Results showed that OPRM1 rs1799971 (p = 0.006) and ABCG2 rs2231142 (p = 0.041) were significantly associated with recovery time. Ten factors after random forest and stepwise selection were associated with recovery time. Ten factors after random forest and stepwise selection were associated with recovery time. Meanwhile, seven factors were associated with delayed recovery. CONCLUSION: This study demonstrated that both clinical and pharmacogenetic data are significantly associated with recovery from general anesthesia and provide the basis for pre-emptive prediction tools.


Asunto(s)
Dolor/genética , Transportador de Casetes de Unión a ATP, Subfamilia G, Miembro 2/genética , Algoritmos , Periodo de Recuperación de la Anestesia , Anestesia General/métodos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Dolor/tratamiento farmacológico , Farmacogenética/métodos , Estudios Prospectivos , Receptores Opioides mu/genética , Factores de Tiempo
3.
Pharmacogenomics ; 19(3): 285-298, 2018 02.
Artículo en Inglés | MEDLINE | ID: mdl-29318929

RESUMEN

General anesthesia is a state of unconsciousness, amnesia, analgesia and akinesia induced by drugs including opioids, hypnotic-sedative agents, muscle relaxants and antiemetics. Clinical and genetic factors are reported to influence the efficacy and side effects of these agents. Based on the evidence, clinical action is needed to improve clinical outcomes. This review summarizes the latest knowledge with regards to the pharmacogenetics of anesthetics and general anesthesia related complications.


Asunto(s)
Anestesia General/métodos , Anestésicos Generales , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/genética , Polimorfismo de Nucleótido Simple , Anestésicos Generales/efectos adversos , Anestésicos Generales/farmacocinética , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/etiología , Humanos , Farmacogenética
4.
Clin Chim Acta ; 471: 216-221, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28601671

RESUMEN

BACKGROUND: Epstein-Barr virus (EBV) and microsatellite instability (MSI) are associated with the carcinogenesis of many kinds of tumors, including gastric cancer (GC). However, the impact of EBV and MSI status on the prognosis of stage II and III GC is still unclear. The aim of this study was to find out the prognostic value of EBV and MSI status in a population of GC patients from Southern China. METHODS: Patients were genotyped for EBV infection based on the detection of EBV DNA from the formalin-fixed paraffin-embedded (FFPE) specimens. Sequentially, MSI status was measured by direct sequencing. Clinical characteristics and overall survival (OS) were analyzed in 202 GC patients. Additionally, the association of EBV and MSI status with chemotherapy-based toxicity was analyzed in 324 GC patients. RESULTS: The survival analysis revealed EBV+ patients had a poorer OS than EBV- patients (HR=1.75, 95% CI: 1.08-2.82, FDR p=0.04). This survival advantage for EBV- patients was also found in patients <60y (FDR p=0.04) and patient with stage III disease (FDR p=0.04). CONCLUSIONS: EBV infection and MSI status are associated with overall survival of gastric cancer patients. However, traditional chemotherapy showed no difference on outcome of patients in EBV and MSI subgroups.


Asunto(s)
Infecciones por Virus de Epstein-Barr/genética , Neoplasias Gástricas/genética , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , ADN de Neoplasias/genética , ADN de Neoplasias/aislamiento & purificación , Femenino , Humanos , Masculino , Inestabilidad de Microsatélites , Persona de Mediana Edad , Neoplasias Gástricas/tratamiento farmacológico , Resultado del Tratamiento
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