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Gut microbiota of patients with different subtypes of gastric cancer and gastrointestinal stromal tumors

Sarhadi, Virinder (författare)
Univ Helsinki, Dept Pathol, Fac Med, Helsinki 00014, Finland.
Mathew, Binu (författare)
Univ Turku, Dept Comp, Turku, Finland.
Kokkola, Arto (författare)
Univ Cent Hosp Helsinki, HUCH Gastrointestinal Clin, Helsinki, Finland.
visa fler...
Karla, Tiina (författare)
Thermo Fisher Sci, Vantaa, Finland.
Tikkanen, Milja (författare)
Thermo Fisher Sci, Vantaa, Finland.
Rautelin, Hilpi (författare)
Uppsala universitet,Klinisk mikrobiologi
Lahti, Leo (författare)
Univ Turku, Dept Comp, Turku, Finland.
Puolakkainen, Pauli (författare)
Univ Cent Hosp Helsinki, HUCH Gastrointestinal Clin, Helsinki, Finland.
Knuutila, Sakari (författare)
Univ Helsinki, Dept Pathol, Fac Med, Helsinki 00014, Finland.
visa färre...
Univ Helsinki, Dept Pathol, Fac Med, Helsinki 00014, Finland Univ Turku, Dept Comp, Turku, Finland. (creator_code:org_t)
2021-02-17
2021
Engelska.
Ingår i: Gut Pathogens. - : BioMed Central (BMC). - 1757-4749. ; 13:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Gastric adenocarcinoma is associated with H. pylori infection and inflammation that can result in the dysbiosis of gastric microbiota. The association of intestinal microbiota with gastric adenocarcinoma subtypes or with gastric gastrointestinal stromal tumors (GIST) is however not well known. Therefore, we performed 16S rRNA gene sequencing on DNA isolated from stool samples of Finnish patients and controls to study differences in microbiota among different histological subtypes of gastric adenocarcinoma, gastric GIST and healthy controls. Results We found that gut microbiota alpha diversity was lowest in diffuse adenocarcinoma patients, followed by intestinal type and GIST patients, although the differences were not significant compared to controls. Beta-diversity analysis however showed significant differences in microbiota composition for all subtypes compared to controls. Significantly higher abundance of Enterobacteriaceae was observed in both adenocarcinoma subtypes, whereas lower abundance of Bifidobacteriaceae was seen only in diffuse adenocarcinoma and of Oscillibacter in intestinal adenocarcinoma. Both GIST and adenocarcinoma patients had higher abundance of Enterobacteriaceae and lower abundance of Lactobacillaceae and Oscillibacter while lower abundance of Lachnoclostridium, Bifidobacterium, Parabacteroides and Barnesiella was seen only in the adenocarcinoma patients. Conclusions Our analysis shows association of higher Enterobacteriaceae abundance with all types of gastric tumors. Therefore it could be potentially useful as a marker of gastric malignancies. Lower gut microbiota diversity might be indicative of poorly differentiated, invasive, advanced or aggressive tumors and could possibly be a prognostic marker for gastric tumors.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Gastroenterologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Diffuse gastric adenocarcinoma
Intestinal gastric adenocarcinoma
GIST
Gut microbiota

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