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Identification of TPM2 and CNN1 as Novel Prognostic Markers in Functionally Characterized Human Colon Cancer-Associated Stromal Cells

Mele, Valentina (author)
University Hospital Basel
Basso, Camilla (author)
Regional Hospital of Lugano,Università della Svizzera Italiana
Governa, Valeria (author)
Lund University,Lunds universitet,Tumörmikromiljö,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Tumörmikromiljön,Forskargrupper vid Lunds universitet,Tumor microenvironment,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund University Research Groups
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Glaus Garzon, Jesus F. (author)
University of Zurich
Muraro, Manuele G. (author)
University Hospital Basel
Däster, Silvio (author)
University Hospital Basel
Nebiker, Christian A. (author)
University Hospital Basel
Mechera, Robert (author)
University Hospital Basel
Bolli, Martin (author)
University Hospital Basel
Schmidt, Alexander (author)
University of Basel
Geiger, Roger (author)
Università della Svizzera Italiana
Spagnoli, Giulio C. (author)
Christoforidis, Dimitri (author)
Università della Svizzera Italiana,Regional Hospital of Lugano
Majno, Pietro E. (author)
Regional Hospital of Lugano,Università della Svizzera Italiana
Borsig, Lubor (author)
University of Zurich
Iezzi, Giandomenica (author)
Università della Svizzera Italiana,Regional Hospital of Lugano
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 (creator_code:org_t)
2022-04-16
2022
English.
In: Cancers. - : MDPI AG. - 2072-6694. ; 14:8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Stromal infiltration is associated with poor prognosis in human colon cancers. However, the high heterogeneity of human tumor-associated stromal cells (TASCs) hampers a clear identification of specific markers of prognostic relevance. To address these issues, we established short-term cultures of TASCs and matched healthy mucosa-associated stromal cells (MASCs) from human primary colon cancers and, upon characterization of their phenotypic and functional profiles in vitro and in vivo, we identified differentially expressed markers by proteomic analysis and evaluated their prognostic significance. TASCs were characterized by higher proliferation and differentiation potential, and enhanced expression of mesenchymal stem cell markers, as compared to MASCs. TASC triggered epithelial–mesenchymal transition (EMT) in tumor cells in vitro and promoted their metastatic spread in vivo, as assessed in an orthotopic mouse model. Proteomic analysis of matched TASCs and MASCs identified a panel of markers preferentially expressed in TASCs. The expression of genes encoding two of them, calponin 1 (CNN1) and tropomyosin beta chain isoform 2 (TPM2), was significantly associated with poor outcome in independent databases and outperformed the prognostic significance of currently proposed TASC markers. The newly identified markers may improve prognostication of primary colon cancers and identification of patients at risk.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

CNN1
colon cancer
prognostic markers
proteomics
TPM2
tumor-associated stromal cells

Publication and Content Type

art (subject category)
ref (subject category)

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