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Association of MAD2 expression with mitotic checkpoint competence in hepatoma cells
Authors:Karen Man-Fong Sze  Yick-Pang Ching  Dong-Yan Jin  Irene Oi-Lin Ng
Affiliation:(1) Department of Biochemistry, University of Hong Kong, Faculty of Medicine, Hong Kong, China;(2) Department of Pathology, University of Hong Kong, Queen Mary Hospital Pokfulam, Room 127B, University Pathology Building, Hong Kong, China
Abstract:
Chromosomal instability (CIN) refers to high rates of chromosomal gains and losses and is a major cause of genomic instability of cells. It is thought that CIN caused by loss of mitotic checkpoint contributes to carcinogenesis. In this study, we evaluated the competence of mitotic checkpoint in hepatoma cells and investigated the cause of mitotic checkpoint defects. We found that 6 (54.5%) of the 11 hepatoma cell lines were defective in mitotic checkpoint control as monitored by mitotic indices and flow-cytometric analysis after treatment with microtubule toxins. Interestingly, all 6 hepatoma cell lines with defective mitotic checkpoint showed significant underexpression of mitotic arrest deficient 2 (MAD2), a key mitotic checkpoint protein. The level of MAD2 underexpression was significantly associated with defective mitotic checkpoint response (p<0.001). In addition, no mutations were found in the coding sequences of MAD2 in all 11 hepatoma cell lines. Our findings suggest that MAD2 deficiency may cause a mitotic checkpoint defect in hepatoma cells.
Keywords:MAD2  Cell cycle control  Mitotic checkpoint  Spindle assembly checkpoint  Hepatocellular carcinoma  Carcinogenesis  Genome instability  Chromosomal instability  Microtubule toxin
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