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DC Field | Value | Language |
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dc.contributor.author | Kalra, S. | - |
dc.contributor.author | Mittal, A. | - |
dc.contributor.author | Gupta, K. | - |
dc.contributor.author | Singhal, V. | - |
dc.contributor.author | Gupta, A. | - |
dc.contributor.author | Mishra, T. | - |
dc.contributor.author | Naidu, S. | - |
dc.contributor.author | Sengupta, D. | - |
dc.contributor.author | Ahuja, G. | - |
dc.date.accessioned | 2021-07-06T18:55:53Z | - |
dc.date.available | 2021-07-06T18:55:53Z | - |
dc.date.issued | 2021-07-07 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/2032 | - |
dc.description.abstract | Ectopically expressed olfactory receptors (ORs) have been linked with multiple clinicallyrelevant physiological processes. Previously used tissue-level expression estimation largely shadowed the potential role of ORs due to their overall low expression levels. Even after the introduction of the single-cell transcriptomics, a comprehensive delineation of expression dynamics of ORs in tumors remained unexplored. Our targeted investigation into single malignant cells revealed a complex landscape of combinatorial OR expression events. We observed differentiation-dependent decline in expressed OR counts per cell as well as their expression intensities in malignant cells. Further, we constructed expression signatures based on a large spectrum of ORs and tracked their enrichment in bulk expression profiles of tumor samples from The Cancer Genome Atlas (TCGA). TCGA tumor samples stratified based on OR-centric signatures exhibited divergent survival probabilities. In summary, our comprehensive analysis positions ORs at the cross-road of tumor cell differentiation status and cancer prognosis. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Analysis of single-cell transcriptomes links enrichment of olfactory receptors with cancer cell differentiation status and prognosis | en_US |
dc.type | Article | en_US |
Appears in Collections: | Year-2020 |
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Fulltext.pdf | 7.36 MB | Adobe PDF | View/Open Request a copy |
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