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Clinicopathological examination of dipeptidase 1 expression in colorectal cancer. | LitMetric

AI Article Synopsis

  • Dipeptidase 1 (DPEP1) is an important enzyme in metabolism, previously thought to suppress tumors but linked to poorer outcomes in colorectal cancer (CRC).
  • * The study investigated DPEP1 expression in CRC tissues using advanced techniques and found higher levels in cancerous versus non-cancerous tissue.
  • * Despite increased DPEP1 correlating with lymph node metastasis, there was no connection with other cancer markers, suggesting a need for more research on its role in CRC.

Article Abstract

Dipeptidase 1 (DPEP1) is a zinc-dependent metalloproteinase that is fundamental in glutathione and leukotriene metabolism. was initially considered as a tumor suppressor gene in Wilms' tumor and breast cancer. However, it has been reported that DPEP1 is upregulated in colorectal cancers (CRCs) and high DPEP1 expression levels are associated with poorer patient survival. The role of genes in CRC, as well as their expression, requires investigation. Therefore, the present study investigated DPEP1 expression using reverse transcription-quantitative polymerase chain reaction or immunohistochemistry on surgically resected samples from CRC cases, and further examined the biological significance of DPEP1 by comparing the expression of the epithelial to mesenchymal transition (EMT) markers, including epithelial cadherin and Vimentin to clarify the function of DPEP1 in CRC, particularly in metastasis. The level of DPEP1 expression was identified to be significantly increased in tumorous tissue samples compared with that in non-tumorous tissue samples. In addition, increased DPEP1 mRNA expression levels were associated with positive lymph node metastasis in the included cohort. However, no positive correlations were observed between DPEP1 and EMT markers in the cohort. The results indiciates that further investigations into the upregulation of DPEP1 in colorectal carcinogenesis and the role of therapeutic or prognostic biomarkers are required.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374953PMC
http://dx.doi.org/10.3892/br.2017.870DOI Listing

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