2019
DOI: 10.3389/fmicb.2019.01458
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Analysis of the Relationship Between the Degree of Dysbiosis in Gut Microbiota and Prognosis at Different Stages of Primary Hepatocellular Carcinoma

Abstract: Gut microbiota dysbiosis is closely associated with primary hepatocellular carcinoma (HCC). Recent studies have evaluated the early diagnosis of primary HCC through analysis of gut microbiota dysbiosis. However, the relationship between the degree of dysbiosis and the prognosis of primary HCC remains unclear. Because primary HCC is accompanied by dysbiosis and dysbiosis usually increases the circulatory concentrations of endotoxin and other harmful bacterial substances, which further increases liver damage, we… Show more

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Cited by 82 publications
(88 citation statements)
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“…The V4-V5 hypervariable region of the prokaryotic 16S rRNA gene was amplified using the universal primer pair 515F and 909R, with a 12-nt sample-specific barcode sequence included at the 5′-end of the 515F sequence to distinguish between samples (Huang et al, 2018;Ni et al, 2019). Polymerase chain reaction was performed and the amplicons were sequenced using a HiSeq system at Guangdong Meilikang Bio-Science, Ltd. (Guangdong, China), as described previously (Ni et al, 2017;Huang et al, 2018;Xiang et al, 2018).…”
Section: Dna Extraction and High-throughput Sequencingmentioning
confidence: 99%
“…The V4-V5 hypervariable region of the prokaryotic 16S rRNA gene was amplified using the universal primer pair 515F and 909R, with a 12-nt sample-specific barcode sequence included at the 5′-end of the 515F sequence to distinguish between samples (Huang et al, 2018;Ni et al, 2019). Polymerase chain reaction was performed and the amplicons were sequenced using a HiSeq system at Guangdong Meilikang Bio-Science, Ltd. (Guangdong, China), as described previously (Ni et al, 2017;Huang et al, 2018;Xiang et al, 2018).…”
Section: Dna Extraction and High-throughput Sequencingmentioning
confidence: 99%
“…PCR was performed, and amplicons were sequenced using a MiSeq system at Guangdong Meilikang Bio-Science, Ltd. (China), as described previously (1). The raw sequences were merged using FLASH-1.2.8 software and processed using the QIIME pipeline 1.9.0 as described previously(1)(19). Chimeric sequences were identified and removed using the Uchime algorithm and the no-chimeric sequences were clustered into OTUs at 97% identity using UPARSE software (20) (21).…”
Section: Methodsmentioning
confidence: 99%
“…The paired-end reads from the raw DNA fragments were merged using FLASH software. The merged tags were assigned to each sample according to the sample-specific barcodes, and the low-quality sequences were detected and removed using QIIME 1.9.0 software according to previous reports (Li et al, 2017; Huang et al, 2018; Ni et al, 2017; Ni et al, 2019). Chimeric sequences were detected and removed using Uchime algorithm (Edgar et al, 2011) embedded to QIIME 1.9.0 software.…”
Section: Methodsmentioning
confidence: 99%