Overexpression of aldolase, fructose-bisphosphate C and its association with spheroid formation in colorectal cancer

Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide. The spheroid colony formation assay is a useful method to identify cancer stem cells (CSCs). Using the DLD-1 and WiDr CRC cell lines, we performed microarray analyses of spheroid body-forming and parental cells and demonstrated that aldolase, fructose-bisphosphate C (ALDOC) was overexpressed in the spheroid body-forming cells of both lines. Cells transfected with small interfering RNA against ALDOC demonstrated lower proliferation, migration, and invasion compared with negative control cells. Both the number and size of spheres produced by the CRC cells were significantly reduced by ALDOC knockdown. Additionally, inhibition of ALDOC reduced lactate production. Immunohistochemistry was used to analyze ALDOC protein expression in tissues from 135 CRC patients and revealed that 66 (49%) cases were positive for ALDOC. The ALDOC-positive cases were associated with higher T and M grades and, as determined by Kaplan-Meier analysis, a poorer prognosis. Univariate and multivariate analyses indicated that ALDOC expression was an independent prognostic factor for CRC patients. Furthermore, ALDOC expression was associated with CD44 expression. These results suggest that ALDOC contributes to CRC progression and plays an important role in CSCs derived from CRC.

Automated summary

Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide. This study found that ALDOC is overexpressed in spheroid-forming cells of CRC and its knockdown leads to reduced proliferation, migration, invasion, and lactate production. ALDOC-positive expression is associated with poorer prognosis in CRC patients and is an independent prognostic factor. ALDOC expression is also associated with CD44 expression, suggesting its important role in CRC progression and cancer stem cells.