AI Article Synopsis

  • Aberrantly activated Notch signaling is implicated in the development and progression of colorectal cancer, leading to the investigation of Notch1 and Notch2 as potential prognostic predictors.
  • In a study of 1003 colorectal cancer specimens, immunohistochemistry revealed that Notch1 and Notch2 protein levels showed a significant negative correlation, indicating opposing roles in tumor behavior.
  • These receptors were found to be inversely related to key clinical factors like tumor differentiation and metastasis, suggesting their potential as independent adverse prognostic indicators for patient outcomes.

Article Abstract

Background: Aberrantly activated Notch signaling has been shown to play a key role in carcinogenesis and progression of various human malignancies. In this study, we investigated the expression of Notch1 and Notch2 in colorectal cancer to determine whether they could serve as prognostic predictors.

Patients And Methods: The protein expression of Notch1 and Notch2 was examined by immunohistochemistry in 1003 clinical colorectal cancer specimens. Notch1 and Notch2 protein levels were investigated by immunohistochemistry. Statistical analysis was carried out to assess their prognostic value.

Results: Significantly negative correlation between Notch1 and Notch2 was found in colorectal cancer (P < 0.001). Notch1 and Notch2 were proved to be inversely correlated with tumor differentiation, depth of invasion, lymph node metastases, distant metastasis, TNM (tumor-node-metastasis) stage and survival of patients, suggesting opposite function of the two receptors. Notch1 and Notch2 were proved to be adverse independent prognostic predictors (P < 0.001). Moreover, a synergistic effect of positive Notch1 and negative Notch2 coexpression on predicting poor overall survival was proved.

Conclusions: Notch1 and Notch2 may be independent adverse prognostic predictors for patients with colorectal cancer. These results would contribute to identify more efficient prognostic predictors and therapeutic targets.

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Source
http://dx.doi.org/10.1093/annonc/mdq776DOI Listing

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