demecolcine and Wilms-Tumor

Skin fibroblast cells from two unrelated male infants with a chromosome-instability disorder were analyzed for their response to colcemid-induced mitotic-spindle checkpoint. The infants both had severe growth and developmental retardation, microcephaly, and Dandy-Walker anomaly; developed Wilms tumor; and one died at age 5 mo, the other at age 3 years. Their metaphases had total premature chromatid separation (total PCS) and mosaic variegated aneuploidy. Mitotic-index analysis of their cells showed the absence of mitotic block after the treatment with colcemid, a mitotic-spindle inhibitor. Bromodeoxyuridine-incorporation measurement and microscopic analysis indicated that cells treated with colcemid entered G1 and S phases without sister-chromatid segregation and cytokinesis. Preparations of short-term colcemid-treated cells contained those cells with chromosomes in total PCS and all or clusters of them encapsulated by nuclear membranes. Cell-cycle studies demonstrated the accumulation of cells with a DNA content of 8C. These findings indicate that the infants' cells were insensitive to the colcemid-induced mitotic-spindle checkpoint.

Topics: Abnormalities, Multiple; Aneuploidy; Cells, Cultured; Child, Preschool; Chromatids; Chromosome Fragility; Chromosome Segregation; Demecolcine; DNA; Fibroblasts; Flow Cytometry; Growth Disorders; Humans; Infant; Male; Metaphase; Mitotic Index; Mosaicism; Nuclear Envelope; Skin; Spindle Apparatus; Syndrome; Wilms Tumor

Topics: Acrylamides; Alkaline Phosphatase; Animals; Cells, Cultured; Cricetinae; Demecolcine; Depression, Chemical; Electrophoresis; HeLa Cells; Histones; Humans; In Vitro Techniques; Mitosis; Neoplasm Proteins; Nucleoproteins; Phosphates; Rats; Vinblastine; Wilms Tumor