Abstract

BackgroundMalignant mesothelioma (MM) is a very aggressive tumor that develops from mesothelial cells, mainly due to asbestos exposure. MM is categorized into three major histological subtypes: epithelioid, sarcomatoid, and biphasic, with the biphasic subtype containing both epithelioid and sarcomatoid components. Patients with sarcomatoid mesothelioma usually show a poorer prognosis than those with epithelioid mesothelioma, but it is not clear how these morphological phenotypes are determined or changed during the oncogenic transformation of mesothelial cells.MethodsWe introduced the E6 and E7 genes of human papillomavirus type 16 and human telomerase reverse transcriptase gene in human peritoneal mesothelial cells and established three morphologically different types of immortalized mesothelial cell lines.ResultsHOMC-B1 cells exhibited epithelioid morphology, HOMC-A4 cells were fibroblast-like, spindle-shaped, and HOMC-D4 cells had an intermediate morphology, indicating that these three cell lines closely mimicked the histological subtypes of MM. Gene expression profiling revealed increased expression of NOD-like receptor signaling-related genes in HOMC-A4 cells. Notably, the combination treatment of HOMC-D4 cells with TGF-β and IL-1β induced a morphological change from intermediate to sarcomatoid morphology.ConclusionsOur established cell lines are useful for elucidating the fundamental mechanisms of mesothelial cell transformation and mesothelial-to-mesenchymal transition.

Highlights

  • Malignant mesothelioma (MM) is a very aggressive tumor that develops from mesothelial cells, mainly due to asbestos exposure

  • Establishment of immortalized mesothelial cell lines To establish immortalized mesothelial cell lines, we first obtained mesothelial cells from the omental tissue, which was resected from a patient with gastric cancer and cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS)

  • Since human primary cells eventually undergo cell cycle arrest after a limited number of cell divisions, we introduced human papillomavirus 16 (HPV16) E6 and E7 genes and human telomerase reverse transcriptase genes into the cells using retroviral vectors to ensure their continuous growth (Fig. 1A)

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Summary

Introduction

Malignant mesothelioma (MM) is a very aggressive tumor that develops from mesothelial cells, mainly due to asbestos exposure. Patients with sarcomatoid mesothelioma usually show a poorer prognosis than those with epithelioid mesothelioma, but it is not clear how these morphological phenotypes are determined or changed during the oncogenic transformation of mesothelial cells. Mesothelial cells have characteristic microvilli at the cell surface, which are thought to play a role in protecting the mesothelium from damage. Malignant mesothelioma (MM) develops from mesothelial cells; the exact mechanism of this process has not yet been clearly determined. MM is caused by asbestos, and clinically overt MM tumors are usually diagnosed after a long latency of ~30–40 years [3, 4]. Curative treatment modalities are still limited for patients with MM, and the prognosis of patients is usually poor [6, 7]

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