[Objective]Provide a theoretical basis for the popularization and application of Jiazhe 91A through the research and analysis on the advantages and characteristics of F1 generation of Jiazhe 91A combinations. [Method]...[Objective]Provide a theoretical basis for the popularization and application of Jiazhe 91A through the research and analysis on the advantages and characteristics of F1 generation of Jiazhe 91A combinations. [Method]The mid-parent heterosis,heterobeltiosis,competitive advantage and average dominance of the F1 generation of the three combinations configured by Jiazhe 91A were analyzed by the comparison and appraisal test of combinations configured by Jiazhe 91A. [Result]the panicle shape of the F1 generation of the three combinations configured by Jiazhe 91A was larger,and the panicles number was greater than its parents,the growing period was shorter than that of Shanyou 63,while the spikelets per panicle,seed setting rate and yield were higher than the control Shanyou 63,and the yield was 2.7% to 12.1% higher than Shanyou 63. [Conclusion]The sterility of Jiazhe 91A sterility was stable,and had a strong restoring ability,so it had widespread application prospects.展开更多
Background:Hepatocellular carcinoma(HCC)is an aggressive and lethal malignancy.Metabolic reprogramming dynamically remodels the tumor microenvironment(TME)and drives HCC progression.This study investigated the mechani...Background:Hepatocellular carcinoma(HCC)is an aggressive and lethal malignancy.Metabolic reprogramming dynamically remodels the tumor microenvironment(TME)and drives HCC progression.This study investigated the mechanism through which metabolic reprogramming remodels the TME in HCC.Methods:HCC patient transcriptome data were subjected to bioinformatics analysis to identify differentially expressed genes and immune infiltration status.Immunohistochemical analysis was performed to determine the correlation between succinate dehydrogenase complex subunit A(SDHA)expression and M2 macrophage infiltration.SDHA-knockdown or SDHA-overexpressing HCC cells were used for in vitro experiments,including co-culturing,flow cytometry,and enzyme-linked immunosorbent assay.Western blotting assay,functional assays,and subcutaneous tumor model mice were used to elucidate the molecular mechanisms underlying succinate-mediated HCC cell-macrophage interactions in the TME.Results:Higher infiltration of M2 macrophages correlated with worse prognosis in HCC patients.SDHA was downregulated in HCC tumor tissues and showed a negative correlation with M2 macrophage infiltration.SDHA knockdown promoted M2 macrophage polarization,whereas SDHA overexpression reversed this effect.Mechanistically,SDHA deficiency in HCC cells induced succinate accumulation,which promoted M2 macrophage polarization by activating the G protein-coupled receptor 91(GPR91)/signal transducer and activator of transcription 3(STAT3)pathway.Concurrently,succinate stimulation enhanced mitochondrial oxidative phosphorylation in M2 macrophages,thereby promoting HCC progression.Serum succinate levels were elevated in HCC patients.The receiver operating characteristic curve analysis indicated that serum succinate is a promising diagnostic marker for HCC(area under the curve=0.815).Conclusion:SDHA deficiency leads to succinate accumulation,which promotes M2 macrophage polarization through the GPR91/STAT3 pathway,thereby facilitating HCC progression.Based on these findings,serum succinate could be a promising diagnostic biomarker for HCC.展开更多
基金Supported by Major Projects of Zhejiang Province -" 8812 " Plan(2004C12020-1-6)Key Scientific and Technological Project of Jiaxing City in Zhejiang Province (2007AZ1001)~~
文摘[Objective]Provide a theoretical basis for the popularization and application of Jiazhe 91A through the research and analysis on the advantages and characteristics of F1 generation of Jiazhe 91A combinations. [Method]The mid-parent heterosis,heterobeltiosis,competitive advantage and average dominance of the F1 generation of the three combinations configured by Jiazhe 91A were analyzed by the comparison and appraisal test of combinations configured by Jiazhe 91A. [Result]the panicle shape of the F1 generation of the three combinations configured by Jiazhe 91A was larger,and the panicles number was greater than its parents,the growing period was shorter than that of Shanyou 63,while the spikelets per panicle,seed setting rate and yield were higher than the control Shanyou 63,and the yield was 2.7% to 12.1% higher than Shanyou 63. [Conclusion]The sterility of Jiazhe 91A sterility was stable,and had a strong restoring ability,so it had widespread application prospects.
基金supported by the Central Government-Guided Local Science and Technology Development Fund Project(Science and Technology Innovation Base Project)(Grant No.236Z7749G)Hebei Provincial Precision Medicine Innovation and Development Joint Fund Incubation Project(Grant No.H2025206547)Hebei Provincial Basic Research Special Youth Science Fund Project(Grant No.H2025206274).
文摘Background:Hepatocellular carcinoma(HCC)is an aggressive and lethal malignancy.Metabolic reprogramming dynamically remodels the tumor microenvironment(TME)and drives HCC progression.This study investigated the mechanism through which metabolic reprogramming remodels the TME in HCC.Methods:HCC patient transcriptome data were subjected to bioinformatics analysis to identify differentially expressed genes and immune infiltration status.Immunohistochemical analysis was performed to determine the correlation between succinate dehydrogenase complex subunit A(SDHA)expression and M2 macrophage infiltration.SDHA-knockdown or SDHA-overexpressing HCC cells were used for in vitro experiments,including co-culturing,flow cytometry,and enzyme-linked immunosorbent assay.Western blotting assay,functional assays,and subcutaneous tumor model mice were used to elucidate the molecular mechanisms underlying succinate-mediated HCC cell-macrophage interactions in the TME.Results:Higher infiltration of M2 macrophages correlated with worse prognosis in HCC patients.SDHA was downregulated in HCC tumor tissues and showed a negative correlation with M2 macrophage infiltration.SDHA knockdown promoted M2 macrophage polarization,whereas SDHA overexpression reversed this effect.Mechanistically,SDHA deficiency in HCC cells induced succinate accumulation,which promoted M2 macrophage polarization by activating the G protein-coupled receptor 91(GPR91)/signal transducer and activator of transcription 3(STAT3)pathway.Concurrently,succinate stimulation enhanced mitochondrial oxidative phosphorylation in M2 macrophages,thereby promoting HCC progression.Serum succinate levels were elevated in HCC patients.The receiver operating characteristic curve analysis indicated that serum succinate is a promising diagnostic marker for HCC(area under the curve=0.815).Conclusion:SDHA deficiency leads to succinate accumulation,which promotes M2 macrophage polarization through the GPR91/STAT3 pathway,thereby facilitating HCC progression.Based on these findings,serum succinate could be a promising diagnostic biomarker for HCC.
