[No authors listed]
Breast cancer affects one in every eight women, and has been associated with higher rates of female mortality than any other cancer type, with the exception of lung cancer. It has been reported that chondromodulin I (ChM-I) was able to suppress tumor angiogenesis and growth in vivo. In order to investigate the antitumor action of ChMâI on human breast cancer cells, a plasmid expressing ChMâI was constructed and transfected into human breast cancer cells using an adenoviral vector. Reverse transcriptionâpolymerase chain reaction detected ChMâI expression in human breast cancer cell lines, whereas no expression was detected in the control groups. In order to assess the effect of ChMâI on human breast cancer cells, cell counting kitâ8 (CCKâ8) and colony formation analyses were used to detect tumor cell proliferation, and the proliferation of ChMâIâtransfected cells was significantly reduced, as compared with the control. In addition, the mRNA expression levels of cell cycleâassociated genes in ChMâIâtransfected cells were significantly decreased, as compared with the control, which suggested that ChMâI transfection was able to inhibit the expression of genes associated with the cell cycle. The results of the present study indicated that ChMâI was able to inhibit the growth of breast cancer cells; thus suggesting that ChM-I may have potential clinical applications in the treatment of breast cancer.
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