Transcriptional response of wild-type and ataxia telangiectasia lymphoblasts following exposure to equitoxic doses of ionizing radiation.

Experiments were designed to compare the transcriptional response to ionizing radiation (IR) of wild-type (WT) and ataxia telangiectasia (AT) cells. mRNA levels were assessed 2, 4 and 24 h after exposure to equitoxic doses using cDNA microarrays. Data reveal distinct patterns of gene expression between AT and WT cells since IR-responsive genes were mostly cell-type specific, this group representing 87 and 94% of the responding genes in WT and AT cells, respectively.

Gene expression profiling of differentiated thyroid neoplasms: diagnostic and clinical implications.

Purpose: The purpose of this research was to identify novel genes that can be targeted as diagnostic and clinical markers of differentiated thyroid tumors.

Experimental Design: Gene expression analysis using microarray platform was performed on 6 pathologically normal thyroid samples and 12 primary follicular and papillary thyroid neoplasms. Microarrays containing probes for 5,760 human full-length cDNAs were used for hybridization with total RNA from normal and tumor thyroid samples labeled with Cy3-dUTP and Cy5-dUTP, respectively.

Progesterone prevents radiation-induced apoptosis in breast cancer cells.

Sex steroid hormones play an essential role in the control of homeostasis in the mammary gland. Although the involvement of progesterone in cellular proliferation and differentiation is well established, its exact role in the control of cell death still remains unclear. As dysregulation of the apoptotic process plays an important role in the pathogenesis of breast cancer, we investigated the regulation of apoptosis by progesterone in various breast cancer cell lines.

Down-regulation of telomerase activity after progesterone treatment of human breast cancer cells: essential role of the cell cycle status.

Steroid hormones have been implicated in the regulation of cellular proliferation and of telomerase activity. Because progestin modulates cell cycle progression in vitro, we investigated if the regulation of telomerase activity by progesterone could be cell cycle-dependent. We found that progesterone treatment of the T47D breast cancer cell line induced both the down-regulation of hTERT (human telomerase reverse transcriptase) mRNA expression and telomerase activity together with a cell cycle blockage characterized by a accumulation of cells in G0/G1-phase.