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Cancer-associated mesothelial cell–derived ANGPTL4 and STC1 promote the early steps of ovarian cancer metastasis
Preety Bajwa, … , Ernst Lengyel, Hilary A. Kenny
Preety Bajwa, … , Ernst Lengyel, Hilary A. Kenny
Published February 16, 2023
Citation Information: JCI Insight. 2023;8(6):e163019. https://doi.org/10.1172/jci.insight.163019.
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Research Article Cell biology Oncology

Cancer-associated mesothelial cell–derived ANGPTL4 and STC1 promote the early steps of ovarian cancer metastasis

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Abstract

Ovarian cancer (OvCa) preferentially metastasizes in association with mesothelial cell–lined surfaces. We sought to determine if mesothelial cells are required for OvCa metastasis and detect alterations in mesothelial cell gene expression and cytokine secretion upon interaction with OvCa cells. Using omental samples from patients with high-grade serous OvCa and mouse models with Wt1-driven GFP-expressing mesothelial cells, we validated the intratumoral localization of mesothelial cells during human and mouse OvCa omental metastasis. Removing mesothelial cells ex vivo from human and mouse omenta or in vivo using diphtheria toxin-mediated ablation in Msln-Cre mice significantly inhibited OvCa cell adhesion and colonization. Human ascites induced angiopoietin-like 4 (ANGPTL4) and stanniocalcin 1 (STC1) expression and secretion by mesothelial cells. Inhibition of STC1 or ANGPTL4 via RNAi obstructed OvCa cell-induced mesothelial cell to mesenchymal transition while inhibition of ANGPTL4 alone obstructed OvCa cell-induced mesothelial cell migration and glycolysis. Inhibition of mesothelial cell ANGPTL4 secretion via RNAi prevented mesothelial cell–induced monocyte migration, endothelial cell vessel formation, and OvCa cell adhesion, migration, and proliferation. In contrast, inhibition of mesothelial cell STC1 secretion via RNAi prevented mesothelial cell–induced endothelial cell vessel formation and OvCa cell adhesion, migration, proliferation, and invasion. Additionally, blocking ANPTL4 function with Abs reduced the ex vivo colonization of 3 different OvCa cell lines on human omental tissue explants and in vivo colonization of ID8p53–/–Brca2–/– cells on mouse omenta. These findings indicate that mesothelial cells are important to the initial stages of OvCa metastasis and that the crosstalk between mesothelial cells and the tumor microenvironment promotes OvCa metastasis through the secretion of ANGPTL4.

Authors

Preety Bajwa, Kasjusz Kordylewicz, Agnes Bilecz, Ricardo R. Lastra, Kristen Wroblewski, Yuval Rinkevich, Ernst Lengyel, Hilary A. Kenny

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Figure 1

Localization of mesothelial cells during OvCa metastasis.

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Localization of mesothelial cells during OvCa metastasis.
(A) IHC locali...
(A) IHC localization of calretinin in omental samples from patients with high-grade serous ovarian cancer (OC) with micrometastases. Black arrows, mesothelial cells (MCs) located on the surface of the omentum and adjacent to OC cells. Black arrowheads, MCs located within the tumor. Red arrows, OC cells. (B) Mouse study design for C and D Wt1tm1(EGFP/Cre)Wtp/J heterozygous mice received an i.p. injection of mCherry-labeled ID8p53–/–Brca2–/– cells and omenta was collected 18 hours and 5 days after injection. (C) IHC localization of mCherry or GFP in mouse omenta. Black arrows, GFP-expressing MCs located on the surface of tumor. Black arrowheadss, GFP-expressing intratumoral MCs. (D) Immunofluorescence. Localization of podoplanin (PDPN, red) and GFP (green) in mouse omenta. Nuclei are stained with Hoechst (blue). Dotted white line is the surface of the tumor/omentum. White arrows point to double-positive MCs on the surface. White arrowheads point to double-positive intratumoral MCs. Scale bar: 500 μm.

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