1.Impact of different eating ways on survival of patients with esophageal perforation after esophageal squamous cell carcinoma radiotherapy
Chuanshan YAO ; Lei MA ; Quanxiao XU ; Chenlu FENG
Chongqing Medicine 2025;54(9):2098-2102
Objective To explore the effects of different eating methods(tube feeding,esophageal stents,intravenous nutrition)on the survival of the patients with esophageal perforation after esophageal squamous cell carcinoma radiotherapy.Methods A retrospective analysis was conducted on the clinical data of 61 inpatients with esophageal perforation after esophageal squamous cell carcinoma radiotherapy in Nanyang Municipal First People's Hospital from January 2013 to December 2022.According to the different perforation sites,they were divided into the esophagomediastinal fistula group(n=38)and esophagotracheal fistula group(n=23).The Kaplan-Meier method was used to evaluate the survival situation of the patients with different eating patterns,and the nutritional status of the patients one in 1 month after esophageal perforation was eval-uated.Results All patients died within 12 months(median survival time was 4.3 months).The 3-month and 6-month survival rates of the patients with tube feeding were 81.2%and 37.5%respectively,those of the pa-tients with esophageal stents were 63.2%and 15.8%,and those of the patients with intravenous nutrition were 40.0%and 0 respectively,and the differences were statistically significant(P<0.05).In the esophago-mediastinal fistula group,the 3-month and 6-month survival rates of the patients with tube feeding were 85.0%and 45.0%respectively,those of patients with esophageal stents were 75.0%and 16.7%respectively,and those of the patients with intravenous nutrition were 50.0%and 0 respectively,and the differences were statistically significant(P<0.05).In the esophagotracheal fistula group,the 3-month and 6-month survival rates of the patients with tube feeding were 75.0%and 25.0%respectively,those of the patients with esopha-geal stents were 42.9%and 14.3%respectively,and those of the patients with intravenous nutrition were 25.0%and 0 respectively,and the differences were not statistically significant(P>0.05).The nutritional sta-tus score of the patients with intravenous nutrition was significantly higher than that of the patients with tube feeding and esophageal stents(P<0.05),but there was no statistically significant difference in the nutritional status score between the patients with tube feeding and the patients with esophageal stents(P>0.05).Conclusion Com-pared with esophageal stents and intravenous nutrition,tube feeding could achieve relatively higher survival rates and better nutritional status.
2.Integrated analysis of gut microbiome and host immune responses in COVID-19.
Xiaoguang XU ; Wei ZHANG ; Mingquan GUO ; Chenlu XIAO ; Ziyu FU ; Shuting YU ; Lu JIANG ; Shengyue WANG ; Yun LING ; Feng LIU ; Yun TAN ; Saijuan CHEN
Frontiers of Medicine 2022;16(2):263-275
Emerging evidence indicates that the gut microbiome contributes to the host immune response to infectious diseases. Here, to explore the role of the gut microbiome in the host immune responses in COVID-19, we conducted shotgun metagenomic sequencing and immune profiling of 14 severe/critical and 24 mild/moderate COVID-19 cases as well as 31 healthy control samples. We found that the diversity of the gut microbiome was reduced in severe/critical COVID-19 cases compared to mild/moderate ones. We identified the abundance of some gut microbes altered post-SARS-CoV-2 infection and related to disease severity, such as Enterococcus faecium, Coprococcus comes, Roseburia intestinalis, Akkermansia muciniphila, Bacteroides cellulosilyticus and Blautia obeum. We further analyzed the correlation between the abundance of gut microbes and host responses, and obtained a correlation map between clinical features of COVID-19 and 16 severity-related gut microbe, including Coprococcus comes that was positively correlated with CD3+/CD4+/CD8+ lymphocyte counts. In addition, an integrative analysis of gut microbiome and the transcriptome of peripheral blood mononuclear cells (PBMCs) showed that genes related to viral transcription and apoptosis were up-regulated in Coprococcus comes low samples. Moreover, a number of metabolic pathways in gut microbes were also found to be differentially enriched in severe/critical or mild/moderate COVID-19 cases, including the superpathways of polyamine biosynthesis II and sulfur oxidation that were suppressed in severe/critical COVID-19. Together, our study highlighted a potential regulatory role of severity related gut microbes in the immune response of host.
COVID-19
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Clostridiales
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Gastrointestinal Microbiome
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Humans
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Immunity
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Leukocytes, Mononuclear
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SARS-CoV-2
3.Inhibitory effect of decorinon invasion of colorectal adenocarcinoma cell line HCT116 in vitro
Chenlu FENG ; Min ZHANG ; Jixia WANG ; Xiangli MENG ; Xiufeng CHU ; Ping LU
Basic & Clinical Medicine 2017;37(6):849-854
Objective To investigate the effect and mechanism of decorin (DCN) on invasion of colorectal cancer cell line HCT116 in vitro.Methods Transwell assay was employed to detect the invasion of HCT116 cells;Real-time PCR was used to detect the expression of CD133 and TIMP-2 mRNA of HCT116 cells;Western blot method was used to detect the expression of HIF-1α, CD133 and TIMP-2 protein of HCT116 cells.Results 1) When the concentrations of DCN was 0, 1 and 3 mg/L, under the conditions of normal oxygen and hypoxia, the numbers of invasive cells were (241±46), (168±46), (51±17) fields in each well (P<0.01) and (207±61), (213±64), (156±54), (44±17) fields in each well (P<0.01).2) Under the normoxic conditions, the TIMP-2 mRNA and protein in HCT116 cells were increased by DCN (3 mg/L) (P<0.01), but that of CD133 were not affected.3) DCN (3 mg/L) significantly decreased the expression of HIF-1α/CD133/TIMP-2 protein in HCT116 cells under hypoxia (P<0.01), but had no significant effect on the expression of CD133 mRNA.ConclusionsUnder the conditions of hypoxia and normal oxygen, DCN may function through different mechanisms to inhibit the invasion of colorectal adenocarcinoma cell line HCT116 in vitro.

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