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Search: L773:1574 7891 OR L773:1878 0261 > Combined RNA/tissue...

Combined RNA/tissue profiling identifies novel Cancer/testis genes

Jamin, Soazik P. (author)
Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France.
Hikmet, Feria (author)
Uppsala universitet,Klinisk och experimentell patologi,Science for Life Laboratory, SciLifeLab
Mathieu, Romain (author)
Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France.;Univ Hosp, Dept Urol, Rennes, France.
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Jégou, Bernard (author)
Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France.
Lindskog, Cecilia (author)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Klinisk och experimentell patologi
Chalmel, Frédéric (author)
Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France.
Primig, Michael (author)
Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France.
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Univ Rennes, INSERM, EHESP, Irset Inst Rech Sante Environm & Travail,UMR S, Rennes, France Klinisk och experimentell patologi (creator_code:org_t)
2021-06-23
2021
English.
In: Molecular Oncology. - : John Wiley & Sons. - 1574-7891 .- 1878-0261. ; 15:11, s. 3003-3023
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Cancer/Testis (CT) genes are induced in germ cells, repressed in somatic cells, and derepressed in somatic tumors, where these genes can contribute to cancer progression. CT gene identification requires data obtained using standardized protocols and technologies. This is a challenge because data for germ cells, gonads, normal somatic tissues, and a wide range of cancer samples stem from multiple sources and were generated over substantial periods of time. We carried out a GeneChip-based RNA profiling analysis using our own data for testis and enriched germ cells, data for somatic cancers from the Expression Project for Oncology, and data for normal somatic tissues from the Gene Omnibus Repository. We identified 478 candidate loci that include known CT genes, numerous genes associated with oncogenic processes, and novel candidates that are not referenced in the Cancer/Testis Database (). We complemented RNA expression data at the protein level for SPESP1, GALNTL5, PDCL2, and C11orf42 using cancer tissue microarrays covering malignant tumors of breast, uterus, thyroid, and kidney, as well as published RNA profiling and immunohistochemical data provided by the Human Protein Atlas (). We report that combined RNA/tissue profiling identifies novel CT genes that may be of clinical interest as therapeutical targets or biomarkers. Our findings also highlight the challenges of detecting truly germ cell-specific mRNAs and the proteins they encode in highly heterogenous testicular, somatic, and tumor tissues.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Cancer
testis genes
GeneChip
Oncogenes
RNA-Sequencing
Tissue microarrays

Publication and Content Type

ref (subject category)
art (subject category)

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