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1000 Titel
  • TGFβ signalling pathway impacts brain metastases profiles in locally advanced colorectal cancer
1000 Autor/in
  1. Jacob, Sven |
  2. Balonov, Ilja |
  3. Jurinovic, Vindi |
  4. Heiliger, Christian |
  5. Tschaidse, Tengis |
  6. Kumbrink, Jörg |
  7. Kirchner, Thomas |
  8. Werner, Jens |
  9. Angele, Martin K. |
  10. Michl, Marlies |
  11. Neumann, Jens |
1000 Verlag Springer Netherlands
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-03-18
1000 Erschienen in
1000 Quellenangabe
  • 41(5):687-697
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10585-024-10277-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11499386/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Rationale</jats:title> <jats:p>Colorectal Cancer (CRC) represents the third most common type of cancer in Germany and the second most common cancer-related cause of death worldwide. Distant metastases are still the main limit for patient survival. While liver metastases as well as peritoneal carcinomatosis can often either be resected or treated with systemic therapy, little options remain for brain metastases. Additionally, a number of studies has already investigated hepatic, peritoneal, pulmonary as well as continuing distant metastases in colorectal cancer. Yet, with respect to tumor biology and brain metastases, little is known so far.</jats:p> </jats:sec><jats:sec> <jats:title>Material and methods</jats:title> <jats:p>Two cohorts, M0 without distant spread and BRA with brain metastases were build. RNA was isolated from paraffin embedded specimen. Gene expression was performed by an RNA NanoString-Analysis using the nCounter® PanCancer Progression Panel by NanoString-Technologies (Hamburg, Germany). Results were analysed by principal component analysis, gene expression and pathway analysis using commonly available databases such as KEGG as benchmark for comparison.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>We were able to determine a gene signature that provides a sophisticated group separation between M0 and BRA using principal component analysis. All genes with strong loading characteristics on principal component 1 were cross-referenced with the subsequently performed accurate gene set enrichment analysis (GSEA). The GSEA revealed a clear dysregulation of the TGFβ pathway in compared cohorts M0 and BRA. Interestingly, the targeted pathways analysis of the identified genes confirmed that in fact almost all strong loading genes of PC1 play a role in the TGFβ pathway.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Our results suggest the TGFβ pathway as a crucial player in the development of brain metastases in primary CRC. In some types of colorectal cancer, downregulation of the TGFβ pathway might hinder primary colorectal cancer to metastasize to the nervous system. While the paradoxical functioning of the TGFβ pathway is still not fully understood, these shed light on yet another clinical implication of this complex pathway.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Gene Expression Regulation, Neoplastic [MeSH]
lokal Female [MeSH]
lokal Brain Neoplasms/secondary [MeSH]
lokal Aged [MeSH]
lokal Adult [MeSH]
lokal TGFβ signalling pathway influences CRC brain metastasis
lokal Humans [MeSH]
lokal Transforming Growth Factor beta/genetics [MeSH]
lokal Middle Aged [MeSH]
lokal Colorectal cancer
lokal Hematogenous spread
lokal Transforming Growth Factor beta/metabolism [MeSH]
lokal Male [MeSH]
lokal Biomarkers, Tumor/metabolism [MeSH]
lokal Research
lokal Colorectal Neoplasms/pathology [MeSH]
lokal Biomarkers, Tumor/genetics [MeSH]
lokal Brain metastasis
lokal Signal Transduction [MeSH]
lokal Colorectal Neoplasms/genetics [MeSH]
lokal Gene Expression Profiling [MeSH]
lokal Gene signature
lokal Pathway analysis
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/SmFjb2IsIFN2ZW4=|https://frl.publisso.de/adhoc/uri/QmFsb25vdiwgSWxqYQ==|https://frl.publisso.de/adhoc/uri/SnVyaW5vdmljLCBWaW5kaQ==|https://frl.publisso.de/adhoc/uri/SGVpbGlnZXIsIENocmlzdGlhbg==|https://frl.publisso.de/adhoc/uri/VHNjaGFpZHNlLCBUZW5naXM=|https://frl.publisso.de/adhoc/uri/S3VtYnJpbmssIErDtnJn|https://frl.publisso.de/adhoc/uri/S2lyY2huZXIsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/V2VybmVyLCBKZW5z|https://frl.publisso.de/adhoc/uri/QW5nZWxlLCBNYXJ0aW4gSy4=|https://frl.publisso.de/adhoc/uri/TWljaGwsIE1hcmxpZXM=|https://frl.publisso.de/adhoc/uri/TmV1bWFubiwgSmVucw==
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  1. Ludwig-Maximilians-Universität München |
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    1000 Förderer Ludwig-Maximilians-Universität München |
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1000 Erstellt am 2025-02-06T01:38:24.620+0100
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1000 Objekt bearb. Tue Aug 05 07:23:34 CEST 2025
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