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Sökning: onr:"swepub:oai:DiVA.org:hj-63214" > Emerging role and c...

Emerging role and clinical implication of mRNA scavenger decapping enzyme in colorectal cancer

Dimberg, Jan (författare)
Jönköping University,HHJ, Avdelningen för klinisk diagnostik,Jönköping Univ, Sch Hlth & Welf, Dept Nat Sci & Biomed, Jönköping, Sweden.
Shamoun, Levar (författare)
Department of Laboratory Medicine and Pathology, Region Jönköping County, Jönköping, Sweden,Dept Lab Med & Pathol, Jönköping, Region Jonkopin, Sweden.
Johansson, Gustaf (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Uppsala Univ, Sweden
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Landerholm, Kalle (författare)
Linköpings universitet,Avdelningen för kirurgi, ortopedi och onkologi,Medicinska fakulteten,Dept Surg, Region Jönköping County, Sweden
Wågsäter, Dick, Professor (författare)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Uppsala Univ, Sweden
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 (creator_code:org_t)
Elsevier, 2023
2023
Engelska.
Ingår i: Pathology, Research and Practice. - : Elsevier. - 0344-0338 .- 1618-0631. ; 253
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Turnover of RNA is a regulated process that in part controls gene expression. This process is partly controlled by the scavenger decapping enzyme (DcpS). This study aimed to investigate the expression of DcpS in colorectal cancer (CRC) tissue, to evaluate its prognostic significance in patients with CRC and to investigate potentially targeted genes by DcpS.METHODS: Immunohistochemical analysis was used to determine localization of DcpS in normal and CRC tissue, western blot analysis for quantification of protein expression and qPCR for mRNA expression in normal and CRC tissue and expression in cell lines after silencing using siRNA. Gene array analysis was used to study regulation of genes after silencing of DcpS. Proliferation was studied using BRDU.RESULTS: DcpS expression was localized to the epithelial cells of both control and cancer tissue. Tumor and paired control tissue samples from 100 patients who underwent surgical resection for primary colorectal adenocarcinomas were utilized. mRNA and protein of DcpS was significantly up-regulated in the patients with CRC and the mRNA level was higher in rectal cancer tissue compared to colon cancer tissue (p < 0.05). Lowest tertile levels of DcpS mRNA in cancer tissue was associated with a decreased cancer-specific survival rate with a hazard ratio (HR) of 4.7 (95% CI=1.02-12.3), independent of disease stage. The low level of DcpS mRNA was a predictor of poorer survival in patients with rectal and disseminated cancer and in patients receiving adjuvant treatment (p < 0.05). After silencing DcpS in Caco-2 cancer cells, altered expression of several genes associated with RNA, cell cycle regulation, alternative splicing and microRNA was observed and resulted in 23% increase in proliferation.CONCLUSIONS: These results indicate that DcpS has potential as a prognostic factor for CRC but further studies in a broader cohort are warranted to evaluate the significance of the findings in the clinic.

Ämnesord

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

Nyckelord

Biomarker
Cancer specific survival
Pathways
Prognostic factor
Silencing

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