Diversity in the extracellular vesicle-derived microbiome of tissues according to tumor progression in pancreatic cancer

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dc.contributor.authorJ Y Jeong-
dc.contributor.authorT B Kim-
dc.contributor.authorJ Kim-
dc.contributor.authorH W Choi-
dc.contributor.authorE J Kim-
dc.contributor.authorH J Yoo-
dc.contributor.authorS Lee-
dc.contributor.authorH R Jun-
dc.contributor.authorWonbeak Yoo-
dc.contributor.authorS Kim-
dc.contributor.authorS C Kim-
dc.contributor.authorE Jun-
dc.date.accessioned2022-04-29T06:14:33Z-
dc.date.available2022-04-29T06:14:33Z-
dc.date.issued2020-
dc.identifier.issn2072-6694-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/25851-
dc.description.abstractThis study was conducted to identify the composition and diversity of the microbiome in tissues of pancreatic cancer and to determine its role. First, extracellular vesicles (EVs) were obtained from the paired tumor and normal tissues, and 16s rRNA gene sequencing was performed. We identified the microbiomes, compared the diversity between groups, and found that Tepidimonas was more abundant in tumors. Second, larger tumors resulted in lower levels of Leuconostoc and Sutterella, and increased lymph node metastasis resulted in higher levels of Comamonas and Turicibacter in tumor tissues. Moreover, in the case of tumor recurrence, the levels of Streptococcus and Akkermansia were decreased in tumor tissues. Finally, with the supernatant of Tepidimonasfonticaldi, proliferation and migration of cells increased, and epithelial-mesenchymal transition and the Tricarboxylic Acid (TCA) cycle-related metabolites were enhanced. The composition and diversity of EV-derived microbiomes are important for providing novel insights into theragnostic approaches in pancreatic cancer.-
dc.publisherMDPI-
dc.titleDiversity in the extracellular vesicle-derived microbiome of tissues according to tumor progression in pancreatic cancer-
dc.title.alternativeDiversity in the extracellular vesicle-derived microbiome of tissues according to tumor progression in pancreatic cancer-
dc.typeArticle-
dc.citation.titleCancers-
dc.citation.number9-
dc.citation.endPage2346-
dc.citation.startPage2346-
dc.citation.volume12-
dc.contributor.affiliatedAuthorWonbeak Yoo-
dc.contributor.alternativeName정진용-
dc.contributor.alternativeName김태범-
dc.contributor.alternativeName김진주-
dc.contributor.alternativeName최희완-
dc.contributor.alternativeName김어진-
dc.contributor.alternativeName유현주-
dc.contributor.alternativeName이송-
dc.contributor.alternativeName전혜령-
dc.contributor.alternativeName유원백-
dc.contributor.alternativeName김석호-
dc.contributor.alternativeName김송철-
dc.contributor.alternativeName전은성-
dc.identifier.bibliographicCitationCancers, vol. 12, no. 9, pp. 2346-2346-
dc.identifier.doi10.3390/cancers12092346-
dc.subject.keywordmicrobiome-
dc.subject.keywordextracellular vesicle-
dc.subject.keywordtissue-
dc.subject.keywordtumor progression-
dc.subject.keywordpancreatic cancer-
dc.subject.localmicrobiome-
dc.subject.localMicrobiom-
dc.subject.localmicrobiom-
dc.subject.localMicrobiome-
dc.subject.localExtracellular vesicle-
dc.subject.localextracellular vesicle-
dc.subject.localExtracellular vesicles-
dc.subject.localTissue-
dc.subject.localtissue-
dc.subject.localTumor Progression-
dc.subject.localTumor progression-
dc.subject.localtumor progression-
dc.subject.localPancreatic cancer-
dc.subject.localpancreatic cancer-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
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