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P4HA2 involved in SLUG-associated EMT predicts poor prognosis of patients with KRAS-positive colorectal cancer. | LitMetric

AI Article Synopsis

  • * The findings revealed that higher levels of SLUG and P4HA2 are linked to worse outcomes, including lympho-vascular invasion, tumor stage, and KRAS mutations, which also correlate with poor overall and disease-free survival.
  • * The research suggests that SLUG and P4HA2 could be significant prognostic biomarkers in CRC, with high P4HA2 expression being a strong independent predictor of tumor recurrence in KRAS mutated cases, pointing to potential new therapeutic strategies.

Article Abstract

This study aimed to examine the immunohistochemical expression of epithelial-mesenchymal transition biomarkers: P4HA2 and SLUG in colorectal carcinoma (CRC) specimens, then to assess their relation to clinicopathological features including KRAS mutations and patients' survival, and finally to study the correlation between them in CRC. The result of this study showed that SLUG and P4HA2 were significantly higher in association with adverse prognostic factors: presence of lympho-vascular invasion, perineural invasion, higher tumor budding, tumor stage, presence of lymph node metastasis, and presence of distant metastasis. CRC specimens with KRAS mutation were associated with significant higher SLUG and P4HA2 expression. High expression of both SLUG and P4HA2 was significantly unfavorable prognostic indicator as regards overall survival (OS) and disease-free survival (DFS). In KRAS mutated cases, high P4HA2 expression was the only significant poor prognostic indicator as regarding DFS. In conclusions, our data highlight that both SLUG and P4HA2 expression may serve as potentially important poor prognostic biomarkers in CRC and targeting these molecules may be providing a novel therapeutic strategy. In KRAS mutation group, high P4HA2 expression is the only independent prognostic factor for tumor recurrence, so it can be suggested to be a novel target for therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11343967PMC
http://dx.doi.org/10.1007/s00795-024-00385-0DOI Listing

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