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Cancer-associated mesothelial cell–derived ANGPTL4 and STC1 promote the early steps of ovarian cancer metastasis
Preety Bajwa, Kasjusz Kordylewicz, Agnes Bilecz, Ricardo R. Lastra, Kristen Wroblewski, Yuval Rinkevich, Ernst Lengyel, Hilary A. Kenny
Preety Bajwa, Kasjusz Kordylewicz, Agnes Bilecz, Ricardo R. Lastra, Kristen Wroblewski, Yuval Rinkevich, Ernst Lengyel, Hilary A. Kenny
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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 6

Treatment with ANGPTL4- or STC1-neutralizing Abs inhibits ovarian metastasis.

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Treatment with ANGPTL4- or STC1-neutralizing Abs inhibits ovarian metast...
(A and B) IHC localization of ANGPTL4 or STC1 in omental samples from a patient with benign disease or patients with high-grade ovarian cancer (OC) with micro-metastases. Black arrows point to mesothelial cells (MCs). Red arrows point to OC. Scale bar: 500 μm. (C and D) ANGPTL4 or STC1 mRNA expression levels in MCs or cancer-associated mesothelial cells (CAMs). HBME-1 positive cells were FACS from benign omentum washes or ascites from patients with high-grade serous OC. Data are shown as the mean ± SEM (n = 3–4). ***P < 0.001 and ****P < 0.0001 using unpaired Student’s t tests. (E) Human ex vivo colonization assay. GFP-labeled Tyk-nu, OVCAR5, or Kuramachi OC cells were seeded on human omental tissue explants. The cultures were untreated or treated with an ANGPTL4 neutralizing Ab, a STC1-neutralizing Ab, the respective control IgGs, or both neutralizing Abs. The cancer cells were digested off the omentum and counted using a fluorescent imaging cytometer. Data are represented as the mean ± SEM (n = 5). **P < 0.01, ***P < 0.001, and ****P < 0.0001 calculated by 1-way ANOVA. (F) Mouse study design for G. (G) C57Bl/6 mice were treated with a control IgG or ANGPTL4 Ab (5mg/kg) for 30 minutes; and 48 hours after pchili/luciferase-labeled OC cell i.p. injection, the mouse omental tissues were collected, digested, and a luciferase assay was performed. Data are shown as the mean ± SEM (n = 5). **P < 0.01 by 1-way ANOVA.

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