5,279 research outputs found
Limitations of CD44v6 amplification for the detection of tumour cells in the blood of colorectal cancer patients
Based on the important role of CD44 splice variants in colorectal cancer progression and metastasis, we evaluated the use of CD44v6 expression to detect and assess the metastatic potential of colorectal tumour cells circulating in peripheral blood. A nested amplification was designed that allowed to detect 10–100 colon cancer cells. This assay was applied to blood samples from healthy donors. Strong signals were detected in all cases, indicating that it cannot be used to detect colorectal carcinoma cells in whole blood. We then included an enrichment step based on the use of an anti-epithelial cells monoclonal antibody (BerEP4) coupled to magnetic beads. The CD44v6 reverse transcription polymerase chain reaction (RT PCR) assay was performed on cDNA synthesized from blood samples treated with these beads. We analysed 18 samples from 12 patients with a gastrointestinal disease, and 36 samples from ten patients with a colorectal cancer. None of the patients used as negative controls were found to contain epithelial cells in their blood as determined by cytokeratin 19 RT-PCR. By contrast, CD44 transcripts containing exon v6 were detected in nine out of the 18 samples tested (50%). For the colorectal cancer patients, six out of the seven samples (85.7%) that were cytokeratin 19-positive were CD44v6-negative, whereas ten samples out of the 29 not containing epithelial cells were CD44v6-positive (34.5%). This is probably due to the persistence of CD8+ leucocytes in the enriched preparations, as determined by PCR analysis of the CD8 α-chain. We conclude that detection of CD44v6 transcripts using a sensitive nested RT-PCR assay has no potential value to detect and characterize colorectal cancer micrometastases from blood, even following an initial enrichment step. © 2000 Cancer Research Campaig
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Orientation and distribution of recent gullies in the southern hemisphere of Mars: observations from HRSC/MEX and MOC/MGS data
Abstract not available
Synchronous Behavior of Two Coupled Electronic Neurons
We report on experimental studies of synchronization phenomena in a pair of
analog electronic neurons (ENs). The ENs were designed to reproduce the
observed membrane voltage oscillations of isolated biological neurons from the
stomatogastric ganglion of the California spiny lobster Panulirus interruptus.
The ENs are simple analog circuits which integrate four dimensional
differential equations representing fast and slow subcellular mechanisms that
produce the characteristic regular/chaotic spiking-bursting behavior of these
cells. In this paper we study their dynamical behavior as we couple them in the
same configurations as we have done for their counterpart biological neurons.
The interconnections we use for these neural oscillators are both direct
electrical connections and excitatory and inhibitory chemical connections: each
realized by analog circuitry and suggested by biological examples. We provide
here quantitative evidence that the ENs and the biological neurons behave
similarly when coupled in the same manner. They each display well defined
bifurcations in their mutual synchronization and regularization. We report
briefly on an experiment on coupled biological neurons and four dimensional ENs
which provides further ground for testing the validity of our numerical and
electronic models of individual neural behavior. Our experiments as a whole
present interesting new examples of regularization and synchronization in
coupled nonlinear oscillators.Comment: 26 pages, 10 figure
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