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1.
J Cancer Res Clin Oncol ; 147(1): 223-233, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-32691153

RESUMO

BACKGROUND: This study was designed to detect patients with early NSCLC with tentatively using the stem signatures associated autoantibodies (AAbs), and to evaluate its latent values in the early diagnosis and precise prognosis prediction. METHODS: The serum concentrations of selective antibodies were quantitated by enzyme-linked immunosorbent assay (ELISA), and a total of 458 cases were enrolled (training set = 401; validation set = 57). TCGA databases were used to analyze the distinct expressions and prognostic values of related genes. The optimal cut-off values were 11.60 U/ml for P53, 4.90 U/ml for MAGEA1, 3.85 U/ml for SOX2, and 7.05U/ml for PGP9.5. RESULTS: We found that the stem signatures associated antibodies of MAGEA1, PGP9.5, SOX2, and TP53 exhibited high expressions in NSCLC, negatively correlating with the overall survival (OS) (P < 0.05). In the test groups, the diagnosis sensitivity of P53, PGP9.5, SOX2, and MAGEA1 reached to 21.5%, 39.0%, 50.3%, and 35.0%, respectively, and the specificity reached to 98.7%, 99.4%, 92.2%, and 97.4%. The four candidates' panel gave a sensitivity of 71.8% with a specificity of 89%. In the validation group, the detection of the four antibodies in early diagnosis of NSCLC also exhibited high specificity and sensitivity, further consolidating their potential application. CONCLUSIONS: The detection regarding stem signatures associated antibodies could be used as effective tools in early NSCLC diagnosis, but not for localized screening of cancers, and their abnormal expression was in accordance with poorer survival.


Assuntos
Autoanticorpos/sangue , Biomarcadores Tumorais/análise , Carcinoma Pulmonar de Células não Pequenas/patologia , Detecção Precoce de Câncer/métodos , Neoplasias Pulmonares/patologia , Células-Tronco Neoplásicas/patologia , Adenocarcinoma de Pulmão/sangue , Adenocarcinoma de Pulmão/imunologia , Adenocarcinoma de Pulmão/patologia , Adenocarcinoma de Pulmão/cirurgia , Autoanticorpos/imunologia , Carcinoma Pulmonar de Células não Pequenas/sangue , Carcinoma Pulmonar de Células não Pequenas/imunologia , Carcinoma Pulmonar de Células não Pequenas/cirurgia , Carcinoma de Células Escamosas/sangue , Carcinoma de Células Escamosas/imunologia , Carcinoma de Células Escamosas/patologia , Carcinoma de Células Escamosas/cirurgia , Feminino , Seguimentos , Humanos , Neoplasias Pulmonares/sangue , Neoplasias Pulmonares/imunologia , Neoplasias Pulmonares/cirurgia , Masculino , Pessoa de Meia-Idade , Células-Tronco Neoplásicas/metabolismo , Prognóstico , Taxa de Sobrevida
2.
J Genet ; 97(1): e1-e12, 2018 Apr 11.
Artigo em Inglês | MEDLINE | ID: mdl-29700269

RESUMO

Improving cotton fibre quality is a major breeding goal for Upland cotton in China.To investigate the genetic mechanisms of fibre quality, a diverse panel of 403 Upland cotton accessions was grown, and the fibre quality traits were measured in six different environments. Genotyping was performed with genomewide simple sequence repeats. A total of 201 markers were polymorphic and generated 394 allele loci, and 403 accessions were arranged into two subgroups using Structure software. Of the marker loci, 18.94% showed significant linkage disequilibrium (P < 0.05). A mixed linear model in association mapping showed that 51 associations were significant between 39 polymorphic loci and five fibre quality traits, according to best linear unbiased prediction, and in at least three of six environments. Of the 39 associated marker loci, 12 were coincident with previous studies. There were 41 typical accessions identified as containing favourable allele loci related to fibre quality traits. The identified favourable QTL alleles and typical accessions for fibre quality are excellent genetic resources for future cotton breeding in China.


Assuntos
Alelos , Mapeamento Cromossômico/métodos , Fibra de Algodão , Estudos de Associação Genética , Genoma de Planta/genética , Gossypium/genética , Característica Quantitativa Herdável , Cruzamento , China , Cromossomos de Plantas , DNA de Plantas , Ecótipo , Marcadores Genéticos , Variação Genética , Genótipo , Desequilíbrio de Ligação/genética , Repetições de Microssatélites , Fenótipo , Polimorfismo Genético , Locos de Características Quantitativas
3.
Journal of Forensic Medicine ; (6): 85-87, 2009.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-983447

RESUMO

OBJECTIVE@#To investigate the expression changes of aquaporins 1 (AQP1) in contused lung tissue of rats and its relationship with pulmonary edema.@*METHODS@#SD rats were randomly divided into experimental and control groups. The pulmonary contusion models were then prepared. The expression and distribution of AQP1 in lung tissue of the rats were detected by immunohistochemistry.@*RESULTS@#The lung tissue showed edema, hemorrhage, inflammatory cell infiltration 1 h, 3 h after pulmonary contusion, and the inflammatory response aggravated after 5 h. AQP1 expression at 1 h, 3 h and 5 h in the contusion group were significantly higher than that of the control group (P < 0.01). The expression of AQP1 continued to increase with time and aggravation of edema compared to the control group. AQP1 was mainly distributed in the capillary endothelial cells and interstitial cells of the bronchial and alveolar walls. Although there were no observed changes in AQP1 expression location in contused lung tissue, the intergrated optical density(IOD) showed significant statistical difference (P < 0.01).@*CONCLUSION@#There might exist an dysregulation of AQPs gene expression in contused lung tissue, leading to a large number of abnormal transmembrane water transportation and abnormal water accumulation, which may be one of the reasons for pulmonary edema in contused lung tissue.


Assuntos
Animais , Feminino , Masculino , Ratos , Aquaporina 1/metabolismo , Contusões/metabolismo , Patologia Legal , Lesão Pulmonar/metabolismo , Edema Pulmonar/metabolismo , Distribuição Aleatória , Ratos Sprague-Dawley
4.
Journal of Forensic Medicine ; (6): 330-332, 2006.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-983215

RESUMO

OBJECTIVE@#To observe pathological changes and apoptosis in rats myocardial cells after Macleaya cordata total alkaloids poisoning, and to provide some references for Macleaya cordata total alkaloids poisoning detection.@*METHODS@#An experimental model of Macleaya cordata total alkaloids poisoning was established, and the technology of TUNEL staining was used.The results were analyzed by computer image analysis competitive system.@*RESULTS@#Quantities of apoptosis in myocardial cells in poisoning groups were much more than those in the control groups at different tages (P<0.01). In addition the quantities of apoptosis were different after different poisoning duration.@*CONCLUSION@#Although clinical symptoms was not obvious and could not be detected by poison analysis. Pathological changes induced by Macleaya cordata total alkaloids could be found through the apoptosis detection.


Assuntos
Animais , Feminino , Masculino , Ratos , Doença Aguda , Apoptose/efeitos dos fármacos , Contagem de Células , Modelos Animais de Doenças , Imuno-Histoquímica , Marcação In Situ das Extremidades Cortadas , Miocárdio/patologia , Miócitos Cardíacos/efeitos dos fármacos , Papaveraceae/química , Papaverina/intoxicação , Distribuição Aleatória , Ratos Sprague-Dawley , Coloração e Rotulagem , Fatores de Tempo
5.
Journal of Forensic Medicine ; (6): 15-17, 2006.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-983119

RESUMO

OBJECTIVE@#To find out the pathological change and the toxic mechanism of Chloranthus serratus Roem. et Schalt in mice.@*METHODS@#Mice were intoxicated by oral administration with extracts of Chloranthus serratus Roem. et Schalt followed by pathological, serum biochemical, and coagulation mechanism examination.@*RESULTS@#The LD50 in mice was 41.12 g/kg; All poisoned mice serum BUN and ALT increased markedly; Thrombocyte decreased and coagulation time increased; The organ index of liver, spleen and kidneys increased significantly; The cells of liver, kidney and heart were degeneration and necrosis, There were extensive hyperemia and hemorrhage in many organs.@*CONCLUSION@#The experiment suggests that the target organs were liver, kidney, heart and blood vessels; The toxic mechanism was the damage on the mitochondrional, endoplasmic reticulum and coagulation system.


Assuntos
Animais , Feminino , Masculino , Camundongos , Biomarcadores/sangue , Relação Dose-Resposta a Droga , Retículo Endoplasmático/efeitos dos fármacos , Patologia Legal , Rim/patologia , Dose Letal Mediana , Fígado/patologia , Magnoliopsida/química , Mitocôndrias Cardíacas/efeitos dos fármacos , Mitocôndrias Hepáticas/efeitos dos fármacos , Miocárdio/patologia , Extratos Vegetais/toxicidade , Distribuição Aleatória
6.
Journal of Forensic Medicine ; (6): 12-14, 2006.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-983118

RESUMO

OBJECTIVE@#In order to improve the accuracy and reliability in sudden cardiac death, the pathogenesis and relationship between the viral myocarditis and dilated cardiomyopathy were investigated.@*METHODS@#Improved immunohistochemical technique was adopted to detect the expression of the dystrophin in myocardium from 25 viral myocarditis, 28 dilated cardiomyopathy and 17 control cases including normal, coronary atherosclerotic heart disease and hypertension heart disease as control.@*RESULTS@#The positive rate of dystrophin protein expression in control group was 100%, that in viral myocarditis was 88%, and that in dilated cardiomyopathy was 57%, There were significant differences among three groups (P<0.05), and the correlation between viral myocarditis and dilated cardiomyopathy group (r = -0.526)were also found.@*CONCLUSION@#The myocardial cytoskeletal protein is disrupted in viral myocarditis and dilated cardiomyopathy, and the dystrophin protein may be involved in the pathogenesis of viral myocarditis and dilated cardiomyopathy. The viral infect and impair heart functions by cleaving host dystrophin proteins may ultimately contributes to the viral myocarditis to the converting from dilated cardiomyopathy.


Assuntos
Feminino , Humanos , Masculino , Cardiomiopatia Dilatada/metabolismo , Estudos de Casos e Controles , Morte Súbita Cardíaca , Distrofina/metabolismo , Infecções por Enterovirus/complicações , Imuno-Histoquímica , Miocardite/virologia , Miocárdio/patologia , Coloração e Rotulagem
7.
Journal of Forensic Medicine ; (6): 81-83, 2003.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-982976

RESUMO

OBJECTIVE@#To study the pathological change and the toxic mechanism of Dioscorea bulbifera L in mice.@*METHODS@#Sixty ICR mice were randomly assigned to four groups poisoned respectively with 200% Dioscorea bulbifera L of 1/4 LD50, 1/10LD50, 1/30LD50 and a control group treated with distilled water by oral administration. All animals were pathologically examined with LM and some of them were examined with TEM when the mice died during the experiment or the survival mice were sacrificed after thirty days.@*RESULTS@#The pathological changes showed fatty change and the increasing glycogen of liver cells; degeneration and necrosis of the epithelia of uriniferous tubules. The serum BUN and ALT of the experimental groups mice were higher than that of control group. Enzyme histochemical staining showed the decreasing activity of G-6-P and SDH in the liver cells in the experimental groups.@*CONCLUSION@#The experiment suggests that the target organs were liver and kidney. The toxic mechanism of Dioscorea bublifera L was the damage of the mitochondrional and endoplasmic reticulum membrane directly. As a result, the activity of the SDH and G-6-P decreased, the metabolism was affected.


Assuntos
Animais , Feminino , Masculino , Camundongos , Doença Hepática Induzida por Substâncias e Drogas/patologia , Dioscorea/toxicidade , Retículo Endoplasmático/patologia , Medicina Legal , Rim/patologia , Camundongos Endogâmicos ICR , Mitocôndrias Hepáticas/patologia , Distribuição Aleatória
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