Objective:To explore the key molecules regulated by norcantharidin(NCTD)in colon cancer treatment.Methods:We used cell counting kit-8 and 5-ethnyl-20-deoxyuridine/Hoechst staining assays to study the effects of NCTD o...Objective:To explore the key molecules regulated by norcantharidin(NCTD)in colon cancer treatment.Methods:We used cell counting kit-8 and 5-ethnyl-20-deoxyuridine/Hoechst staining assays to study the effects of NCTD on cell proliferation in colon cancer.Annexin V-fluorescein isothiocyanate/propidium iodide staining was used to evaluate apoptosis,whereas Transwell assays were conducted to evaluate migration and invasion.We performed RNA sequencing to analyze the changes in gene expression after treatment.Differential analysis was performed using differential expression sequencing 2(Deseq2)in R.Cytoscape was used to construct a competing endogenous RNA(ceRNA)network and Gene Expression Omnibus(GEO)datasets were used to validate sine oculis homeobox homolog 4(SIX4)expression in colon cancer tissues.Furthermore,the prognostic potential of SIX4 was evaluated using receiver-oper-ating characteristic curves.We conducted an immune infiltration analysis to explore the SIX4 relation-ship with the immune microenvironment in colon cancer.Finally,SIX4 expression,pan-cancer prognosis,tumor mutation burden(TMB)correlations,microsatellite instability(MSI),and mismatch repair(MMR)were analyzed.Results:NCTD inhibited colon cancer cell proliferation(P<0.0001),induced apoptosis(P=0.0007),and suppressed the migration and invasion of colon cancer cells.The H19/miR-193b-3p/SIX4 axis was identified as the key ceRNA network involved in the anticancer activity of NCTD.SIX4 is highly expressed in colon cancer tissues,shortening patient survival and affecting immune infiltration.A pan-cancer analysis showed that SIX4 overexpression affects the survival of various cancers.Finally,we correlated SIX4 expression with TMB,MSI,and MMR expression.Conclusion:NCTD inhibits the malignant behaviour of colon cancer cells.SIX4 is abnormally expressed in multiple tumor types,significantly affecting the overall survival of patients with cancer,and is a core regulatory target of NCTD in the treatment of colon cancer.展开更多
The aim of this research work was to enhance the fermentative production of exopolysaccharide(EPS)with mixed fruit waste as a key substrate.Xanothomonas campestries was isolated from spoiled orange and its EPS product...The aim of this research work was to enhance the fermentative production of exopolysaccharide(EPS)with mixed fruit waste as a key substrate.Xanothomonas campestries was isolated from spoiled orange and its EPS production efficiency was determined using EPS medium.Prior to optimisation,the production was 3.4 g/L,upon optimizing the medium the production improved to 9.2 g/L.The medium formulation was studied by sequential addition of medium components and replacement of sugar with mixed fruit waste.In formulated medium,the production enhanced to 11.1 g/L.For further optimisation,the response surface methodology was used,which resulted in the enhancement of production to 14.5 g/L.The scale-up study was undertaken in a 10 L shake flask and fermenter.In 10 L flask EPS,production was 14.45 g/L in 100 h,whereas in 10 L fermenter it was 21.10 g/L in 60h only.The optimisation studies gave nearly 500%(6.2fold)enhanced EPS production and dwindle in fermentation time.Replacement of sucrose with fruit waste extract made the process environment-friendly;omission of L-cystine and use of 50%reduced amount of sodium acetate in the medium lowered the production cost of EPS.The developed process resulted in the utilization of fruit waste and was also useful in solving the fruit waste disposal problem.展开更多
基金funded by the National Natural Science Foundation of China(82074284)China National Traditional Chinese Medicine Inheritance and Innovation Team Sub-project(ZYYCXTD-C-202005-10)+1 种基金China Medical Association of Minorities Research Project(2020MZ298-110101)Open Fund Project,Associated Key Laboratory of Traditional Mongolia Medicine Research and Development,National Ethnic Affairs Commission and Ministry of Education of China(MDK2020013).
文摘Objective:To explore the key molecules regulated by norcantharidin(NCTD)in colon cancer treatment.Methods:We used cell counting kit-8 and 5-ethnyl-20-deoxyuridine/Hoechst staining assays to study the effects of NCTD on cell proliferation in colon cancer.Annexin V-fluorescein isothiocyanate/propidium iodide staining was used to evaluate apoptosis,whereas Transwell assays were conducted to evaluate migration and invasion.We performed RNA sequencing to analyze the changes in gene expression after treatment.Differential analysis was performed using differential expression sequencing 2(Deseq2)in R.Cytoscape was used to construct a competing endogenous RNA(ceRNA)network and Gene Expression Omnibus(GEO)datasets were used to validate sine oculis homeobox homolog 4(SIX4)expression in colon cancer tissues.Furthermore,the prognostic potential of SIX4 was evaluated using receiver-oper-ating characteristic curves.We conducted an immune infiltration analysis to explore the SIX4 relation-ship with the immune microenvironment in colon cancer.Finally,SIX4 expression,pan-cancer prognosis,tumor mutation burden(TMB)correlations,microsatellite instability(MSI),and mismatch repair(MMR)were analyzed.Results:NCTD inhibited colon cancer cell proliferation(P<0.0001),induced apoptosis(P=0.0007),and suppressed the migration and invasion of colon cancer cells.The H19/miR-193b-3p/SIX4 axis was identified as the key ceRNA network involved in the anticancer activity of NCTD.SIX4 is highly expressed in colon cancer tissues,shortening patient survival and affecting immune infiltration.A pan-cancer analysis showed that SIX4 overexpression affects the survival of various cancers.Finally,we correlated SIX4 expression with TMB,MSI,and MMR expression.Conclusion:NCTD inhibits the malignant behaviour of colon cancer cells.SIX4 is abnormally expressed in multiple tumor types,significantly affecting the overall survival of patients with cancer,and is a core regulatory target of NCTD in the treatment of colon cancer.
基金We are grateful to the Department of Science and Technology(DST),New Delhi,India awarding INSPIRE Fellowship to Dr.Kinjal.H.Upadhyay.Dr Bhargav C Patel for correction of text and plagiarism check.
文摘The aim of this research work was to enhance the fermentative production of exopolysaccharide(EPS)with mixed fruit waste as a key substrate.Xanothomonas campestries was isolated from spoiled orange and its EPS production efficiency was determined using EPS medium.Prior to optimisation,the production was 3.4 g/L,upon optimizing the medium the production improved to 9.2 g/L.The medium formulation was studied by sequential addition of medium components and replacement of sugar with mixed fruit waste.In formulated medium,the production enhanced to 11.1 g/L.For further optimisation,the response surface methodology was used,which resulted in the enhancement of production to 14.5 g/L.The scale-up study was undertaken in a 10 L shake flask and fermenter.In 10 L flask EPS,production was 14.45 g/L in 100 h,whereas in 10 L fermenter it was 21.10 g/L in 60h only.The optimisation studies gave nearly 500%(6.2fold)enhanced EPS production and dwindle in fermentation time.Replacement of sucrose with fruit waste extract made the process environment-friendly;omission of L-cystine and use of 50%reduced amount of sodium acetate in the medium lowered the production cost of EPS.The developed process resulted in the utilization of fruit waste and was also useful in solving the fruit waste disposal problem.
