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. 2023 Dec;43(12):2776-2793.
doi: 10.1111/liv.15751. Epub 2023 Oct 7.

Intrinsic cancer cell phosphoinositide 3-kinase δ regulates fibrosis and vascular development in cholangiocarcinoma

Vanessa Bou Malham  1   2 , Nassima Benzoubir  1   2 , Javier Vaquero  3   4 , Christophe Desterke  5 , Jean Agnetti  1   2 , Pei Xuan Song  1   2 , Ester Gonzalez-Sanchez  3   6   7   8 , Ander Arbelaiz  3 , Sophie Jacques  9 , Emanuel Di Valentin  10 , Souad Rahmouni  9 , Tuan Zea Tan  11 , Didier Samuel  1   2   12 , Jean Paul Thiery  13 , Mylène Sebagh  1   2   14 , Laura Fouassier  3 , Ama Gassama-Diagne  1   2
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Free article

Intrinsic cancer cell phosphoinositide 3-kinase δ regulates fibrosis and vascular development in cholangiocarcinoma

Vanessa Bou Malham et al. Liver Int. 2023 Dec.
Free article

Abstract

Background & aims: The class I- phosphatidylinositol-3 kinases (PI3Ks) signalling is dysregulated in almost all human cancers whereas the isoform-specific roles remain poorly investigated. We reported that the isoform δ (PI3Kδ) regulated epithelial cell polarity and plasticity and recent developments have heightened its role in hepatocellular carcinoma (HCC) and solid tumour progression. However, its role in cholangiocarcinoma (CCA) still lacks investigation.

Approach & results: Immunohistochemical analyses of CCA samples reveal a high expression of PI3Kδ in the less differentiated CCA. The RT-qPCR and immunoblot analyses performed on CCA cells stably overexpressing PI3Kδ using lentiviral construction reveal an increase of mesenchymal and stem cell markers and the pluripotency transcription factors. CCA cells stably overexpressing PI3Kδ cultured in 3D culture display a thick layer of ECM at the basement membrane and a wide single lumen compared to control cells. Similar data are observed in vivo, in xenografted tumours established with PI3Kδ-overexpressing CCA cells in immunodeficient mice. The expression of mesenchymal and stemness genes also increases and tumour tissue displays necrosis and fibrosis, along with a prominent angiogenesis and lymphangiogenesis, as in mice liver of AAV8-based-PI3Kδ overexpression. These PI3Kδ-mediated cell morphogenesis and stroma remodelling were dependent on TGFβ/Src/Notch signalling. Whole transcriptome analysis of PI3Kδ using the cancer cell line encyclopedia allows the classification of CCA cells according to cancer progression.

Conclusions: Overall, our results support the critical role of PI3Kδ in the progression and aggressiveness of CCA via TGFβ/src/Notch-dependent mechanisms and open new directions for the classification and treatment of CCA patients.

Keywords: EMT; extracellular-matrix; stemness; tumour growth; vasculature development.

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References

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