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Home › Dataset Library › Transcription profiling of human CD3+ T lymphocytes from patients with Sazary Syndrome

Dataset: Transcription profiling of human CD3+ T lymphocytes from patients with Sazary Syndrome

This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal...

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This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal aberrations. Our data identified recurrent losses of 17p13.2-p11.2 and 10p12.1-q26.3 occurring in 71 and 68% of cases respectively; common gains were detected for 17p11.2-q25.3 (64%) and chromosome 8/8q (50%). Moreover, we identified novel genomic lesions recurring in more than 30% of tumours: loss of 9q13-q21.33 and gain of 10p15.3-10p12.2. In the Sézary Syndrome cases analysed, we could find several small and few large Uniparental Disomies involving interstitial or telomeric regions of LOH occurring mainly for chromosome 10 and to a lesser extent for chromosome 9 and 17. In the attempt to correlate Copy Number data and clinical parameters we find a relationship between complex pattern of chromosomal aberrations, involving at least three recurrent Copy Number alterations, and shorter survival. Integrating mapping and transcriptional data we were able to identify a total of 113 deregulated transcripts in aberrant chromosomal regions that included cancer related genes such as members of the NF-kB pathway (BAG4, BTRC, NKIRAS2, PSMD3, TRAF2) that might explain its constitutive activation in CTCL. Matching this list of genes with those discriminating patients with different survival times we identify several common candidates that might exert critical roles in Sézary Syndrome, like BUB3 and PIP5K1B. Experiment Overall Design: Affymetrix Gene Expression arrays were performed, according to the manufacturer's directions, on RNA extracted from cryopreserved lymphomonocytes purified by Ficoll density gradient centrifugation and positive selection using anti-human CD3-conjugated dynabeads (tumour samples). Gene expression analyses of Affymetrix HG-U133 A arrays were performed for 32 tumour samples.

Species:
human

Samples:
32

Source:
E-GEOD-17601

Updated:
Dec.12, 2014

Registered:
Jun.19, 2014


Factors: (via ArrayExpress)
Sample
GSE17601GSM439390
GSE17601GSM439391
GSE17601GSM439392
GSE17601GSM439393
GSE17601GSM439394
GSE17601GSM439395
GSE17601GSM439396
GSE17601GSM439397
GSE17601GSM439398
GSE17601GSM439399
GSE17601GSM439400
GSE17601GSM439401
GSE17601GSM439402
GSE17601GSM439403
GSE17601GSM439404
GSE17601GSM439405
GSE17601GSM439406
GSE17601GSM439407
GSE17601GSM439408
GSE17601GSM439409
GSE17601GSM439410
GSE17601GSM439411
GSE17601GSM439412
GSE17601GSM439413
GSE17601GSM439414
GSE17601GSM439415
GSE17601GSM439416
GSE17601GSM439417
GSE17601GSM439418
GSE17601GSM439419
GSE17601GSM439420
GSE17601GSM439421

Tags

  • cancer
  • chromosome
  • syndrome

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