Key result
Baseline median serum claudin-1 and claudin-7 levels were significantly lower in patients with colorectal cancer compared to healthy controls (8.4 vs 9.5 ng/ml, P=0.005; 11.57 vs 26.64 ng/ml, P<0.001).
Why the study?
Do serum CLDN1 and CLDN7 levels correlate with diagnosis and survival in patients with colorectal cancer?
Case-Control (n=180)
Yes
Do serum CLDN1 and CLDN7 levels correlate with diagnosis and survival in patients with colorectal cancer?
Reduced serum levels of CLDN1 and CLDN7 may serve as useful diagnostic markers for colorectal cancer, though they do not appear to predict survival outcomes.
May support serum claudins as diagnostic adjuncts in colorectal cancer; leaves open prognostic value pending prospective validation.
The present study aimed to investigate the serum levels and clinical relevance of claudin (CLDN) 1 and CLDN7 in patients with colorectal cancer (CRC). A total of 140 patients with a pathologically confirmed diagnosis of CRC were enrolled in this study. The serum levels of CLDN1 and CLDN7 were determined using the solid-phase sandwich ELISA method. A total of 40 healthy age- and gender-matched controls were included in the analysis. The median age of the patients was 60 years (range, 24-84 years). The localization of the tumor in the majority of the patients was the colon (n=81, 58%). Of the 55 metastatic patients who received palliative chemotheraphy, 31% were chemotherapy-responsive. The baseline median serum CLDN1 and CLDN7 levels were significantly lower in non-metastatic and metastatic patients compared with those in healthy controls (CLND1, P=0.008 and 0.002; and CLND7, P=0.002 and 0.002, respectively). Moreover, known clinical variables, including poor performance status and high carcinoembryonic antigen (CEA) levels were found to be associated with lower serum CLDN1 concentrations for all patients (P=0.03 and P=0.03, respectively). High T stage and high CEA levels were found to be correlated with lower serum CLDN7 concentrations for all patients (P=0.04 and 0.03, respectively). A correlation was identified between CLDN1 and CLDN7 levels in non-metastatic and metastatic CRC patients (both P-values <0.001). Our study results did not reveal any statistical significance for serum CLDN1 or CLND7 concentrations regarding progression-free and overall survival rate. Therefore, reduced serum levels of CLDN1 and CLND7 may be useful markers in the differential diagnosis of CRC.
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Karabulut et al. (2015) conducted a case-control in Colorectal cancer (n=180). Serum claudin-1 and claudin-7 levels vs. Healthy controls was evaluated on Baseline median serum CLDN1 level (ng/ml) (p=0.005). Baseline median serum claudin-1 and claudin-7 levels were significantly lower in patients with colorectal cancer compared to healthy controls (8.4 vs 9.5 ng/ml, P=0.005; 11.57 vs 26.64 ng/ml, P<0.001).
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