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Topics {✒️}

cancer cell-adipocyte interaction/crosstalk pre-publication history emt-inducing transcription factors article download pdf precise multi-cancer invasion epithelial-mesenchymal transition mesenchymal-epithelial transition cancer-type-specific stage suggests emt-specific gene expression transcription factor slug weiyi cheng & jianzhong huang slug-based emt slug-based signature originally obtained full size image epithelial-mesenchymal transitions underlying biological mechanism bmc med genomics mesenchymal transition process emt-related transition invasiveness remain unclear real-time pcr mesenchymal transition signature core epithelial related subjects investigate gene expression gene expression omnibus privacy choices/manage cookies gene expression analysis gene expression signature full access bmc cancer 11 mesenchymal stem cell inhba-transfected ngp cells breast cancer invasion emt core signature ovarian cancer development epithelio-mesenchymal transformation human cancer cells tumour progression underlying biological mechanisms full size table cancer stem cells cells express nat rev cancer motrescu er emt generates cells metastasis-inhibiting therapeutics biomed central article anastassiou

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WebPage:
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         headline:Human cancer cells express Slug-based epithelial-mesenchymal transition gene expression signature obtained in vivo
         description:The biological mechanisms underlying cancer cell motility and invasiveness remain unclear, although it has been hypothesized that they involve some type of epithelial-mesenchymal transition (EMT). We used xenograft models of human cancer cells in immunocompromised mice, profiling the harvested tumors separately with species-specific probes and computationally analyzing the results. Here we show that human cancer cells express in vivo a precise multi-cancer invasion-associated gene expression signature that prominently includes many EMT markers, among them the transcription factor Slug, fibronectin, and α-SMA. We found that human, but not mouse, cells express the signature and Slug is the only upregulated EMT-inducing transcription factor. The signature is also present in samples from many publicly available cancer gene expression datasets, suggesting that it is produced by the cancer cells themselves in multiple cancer types, including nonepithelial cancers such as neuroblastoma. Furthermore, we found that the presence of the signature in human xenografted cells was associated with a downregulation of adipocyte markers in the mouse tissue adjacent to the invasive tumor, suggesting that the signature is triggered by contextual microenvironmental interactions when the cancer cells encounter adipocytes, as previously reported. The known, precise and consistent gene composition of this cancer mesenchymal transition signature, particularly when combined with simultaneous analysis of the adjacent microenvironment, provides unique opportunities for shedding light on the underlying mechanisms of cancer invasiveness as well as identifying potential diagnostic markers and targets for metastasis-inhibiting therapeutics.
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      headline:Human cancer cells express Slug-based epithelial-mesenchymal transition gene expression signature obtained in vivo
      description:The biological mechanisms underlying cancer cell motility and invasiveness remain unclear, although it has been hypothesized that they involve some type of epithelial-mesenchymal transition (EMT). We used xenograft models of human cancer cells in immunocompromised mice, profiling the harvested tumors separately with species-specific probes and computationally analyzing the results. Here we show that human cancer cells express in vivo a precise multi-cancer invasion-associated gene expression signature that prominently includes many EMT markers, among them the transcription factor Slug, fibronectin, and α-SMA. We found that human, but not mouse, cells express the signature and Slug is the only upregulated EMT-inducing transcription factor. The signature is also present in samples from many publicly available cancer gene expression datasets, suggesting that it is produced by the cancer cells themselves in multiple cancer types, including nonepithelial cancers such as neuroblastoma. Furthermore, we found that the presence of the signature in human xenografted cells was associated with a downregulation of adipocyte markers in the mouse tissue adjacent to the invasive tumor, suggesting that the signature is triggered by contextual microenvironmental interactions when the cancer cells encounter adipocytes, as previously reported. The known, precise and consistent gene composition of this cancer mesenchymal transition signature, particularly when combined with simultaneous analysis of the adjacent microenvironment, provides unique opportunities for shedding light on the underlying mechanisms of cancer invasiveness as well as identifying potential diagnostic markers and targets for metastasis-inhibiting therapeutics.
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