AI Article Synopsis

  • Colorectal carcinoma (CRC) is a prevalent type of cancer in western countries, and circulating tumor cells (CTCs) in patients' blood offer insights into prognosis and treatment prediction.
  • The study examined CTC-associated markers (CK20, PLS3, LAD1, DEFA5) in patients with benign inflammatory intestinal disease (IID) to assess their potential for early CRC detection and differentiation from benign conditions.
  • Results indicated that while DEFA5 levels were higher in CRC and IID compared to healthy individuals, CK20 and PLS3 had lower levels in CRC, suggesting that PLS3 may help distinguish between malignant and non-malignant conditions but needs further validation for early detection of CRC.

Article Abstract

Colorectal carcinoma (CRC) belongs to the most common tumor entities in western countries. Circulating tumor cells (CTC) in blood of CRC patients are a powerful prognostic and predictive biomarker. However, whether CTC-associated markers can also be used for early CRC detection and discrimination from benign diseases is not known. This study investigated the presence of CTC-associated markers CK20, PLS3, LAD1, and DEFA5 in blood of patients with benign inflammatory intestinal disease (IID) and their correlation with malignancy. The detection rate of CK20 and DEFA5 significantly differed between diseased patients and healthy controls. LAD1 and PLS3 were detected in all samples with clear differences in gene expression. DEFA5 expression was higher in CRC and IID patients compared to healthy donors, while CK20 and PLS3 were lower in CRC compared to IID patients or healthy controls. Overall, all CTC-associated markers were detectable in blood of IID patients, but not correlating with inflammation severity. Finally, PLS3 emerged as a suitable marker for differentiation between malignant and non-malignant intestinal diseases or healthy controls, however its suitability for early CRC detection needs to be further validated.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750406PMC
http://dx.doi.org/10.3390/cancers14010047DOI Listing

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