Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells

IntroductionRadiotherapy represents a major treatment option for patients with pancreatic cancer, however, its benefits remain limited also due to the ability of cancer cells to migrate to the surrounding tissues. Low-LET ionizing radiation is well known to promote tumor cell migration and invasion,...

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Main Authors: Alexandra Charalampopoulou, Amelia Barcellini, Mario Ciocca, Riccardo Di Liberto, Francesca Pasi, Marco Giuseppe Pullia, Ester Orlandi, Angelica Facoetti
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Oncology
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Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.1003494/full
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author Alexandra Charalampopoulou
Amelia Barcellini
Mario Ciocca
Riccardo Di Liberto
Francesca Pasi
Marco Giuseppe Pullia
Ester Orlandi
Angelica Facoetti
author_facet Alexandra Charalampopoulou
Amelia Barcellini
Mario Ciocca
Riccardo Di Liberto
Francesca Pasi
Marco Giuseppe Pullia
Ester Orlandi
Angelica Facoetti
author_sort Alexandra Charalampopoulou
collection DOAJ
description IntroductionRadiotherapy represents a major treatment option for patients with pancreatic cancer, however, its benefits remain limited also due to the ability of cancer cells to migrate to the surrounding tissues. Low-LET ionizing radiation is well known to promote tumor cell migration and invasion, nevertheless, little data provided by studies using high-LET radiation has led to ambiguous findings. What is hypothesized to be fundamental in the modulation of migration of tumor cells exposed to ionizing radiation is the influence of the microenvironment. Therefore, the properties of cells that populate the tumor stroma cannot be ignored when studying the influence of radiation on the migratory and invasive capacity of cancer cells. This is especially important in the case of pancreatic malignancies that are characterized by an abundance of stromal cells, including cancer-associated fibroblasts, which are known to orchestrate the cross-talk with tumor cells.AimThe current study aims to investigate whether the presence of factors released by irradiated fibroblasts affects the migratory and invasive capacity of pancreatic cancer cells exposed to different doses of photons or C-ions.Materials and methodsAsPC-1 and AG01522 cells were irradiated with the same dose of photons or C-ions at room temperature. Through Boyden chamber assay, we tested whether factors secreted by irradiated fibroblasts may influence tumor cell migration, while the invasiveness of AsPC-1 cells was assessed using matrigel precoated inserts in which medium collected from non-irradiated (0 Gy), photon and C-ion irradiated fibroblasts, was added. Data were analyzed by Student t-test using GraphPad software. The mean ± s.d. was determined with a significance level of p<0.05.ResultsIn the presence of conditioned medium collected from 1 Gy and 2 Gy photon irradiated fibroblasts, the number of migrated tumor cells increased (P<0.0360, P<0.0001) but decreased at 4 Gy dose (P<0.002). There was a trend of reduction in migration (P<0.0460, P<0.038, P<0.0024, P<0.0002), as well as a decrease in invasiveness (P<0.0525, P<0.0035, P<0.0868, P<0.0310) after exposure to 0.5 Gy, 1 Gy, 2 Gy and 4 Gy of C-ions.ConclusionsThe presence of irradiated fibroblasts affected the invasiveness capability of pancreatic cancer cells, probably by the reciprocal release of soluble factors whose production is differently modulated after high or low-LET radiation. Understanding the effects of irradiation on the metastatic potential of pancreatic cancer cells is of utmost importance for improving the outcome and tailoring the therapeutic approach. This challenging scenario requires a continuous and multidisciplinary approach that involves clinicians together with researcher experts in oncological and radiation treatment. In the last years, including preclinical experiences in a multidisciplinary approach has proved to be a winning strategy in clinical oncological research.
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spelling doaj.art-515d15f45eb84841a6eeabe32f4e62ac2022-12-22T04:30:14ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-10-011210.3389/fonc.2022.10034941003494Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cellsAlexandra Charalampopoulou0Amelia Barcellini1Mario Ciocca2Riccardo Di Liberto3Francesca Pasi4Marco Giuseppe Pullia5Ester Orlandi6Angelica Facoetti7Research and Development Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyClinical Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyMedical-Physics Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyDepartment of Medical Physics, IRCCS Policlinico San Matteo Foundation, Pavia, ItalyMedical Oncology Unit, IRCCS Policlinico San Matteo Foundation, Pavia, ItalyResearch and Development Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyClinical Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyResearch and Development Department, National Center for Oncological Hadrontherapy (CNAO), Pavia, ItalyIntroductionRadiotherapy represents a major treatment option for patients with pancreatic cancer, however, its benefits remain limited also due to the ability of cancer cells to migrate to the surrounding tissues. Low-LET ionizing radiation is well known to promote tumor cell migration and invasion, nevertheless, little data provided by studies using high-LET radiation has led to ambiguous findings. What is hypothesized to be fundamental in the modulation of migration of tumor cells exposed to ionizing radiation is the influence of the microenvironment. Therefore, the properties of cells that populate the tumor stroma cannot be ignored when studying the influence of radiation on the migratory and invasive capacity of cancer cells. This is especially important in the case of pancreatic malignancies that are characterized by an abundance of stromal cells, including cancer-associated fibroblasts, which are known to orchestrate the cross-talk with tumor cells.AimThe current study aims to investigate whether the presence of factors released by irradiated fibroblasts affects the migratory and invasive capacity of pancreatic cancer cells exposed to different doses of photons or C-ions.Materials and methodsAsPC-1 and AG01522 cells were irradiated with the same dose of photons or C-ions at room temperature. Through Boyden chamber assay, we tested whether factors secreted by irradiated fibroblasts may influence tumor cell migration, while the invasiveness of AsPC-1 cells was assessed using matrigel precoated inserts in which medium collected from non-irradiated (0 Gy), photon and C-ion irradiated fibroblasts, was added. Data were analyzed by Student t-test using GraphPad software. The mean ± s.d. was determined with a significance level of p<0.05.ResultsIn the presence of conditioned medium collected from 1 Gy and 2 Gy photon irradiated fibroblasts, the number of migrated tumor cells increased (P<0.0360, P<0.0001) but decreased at 4 Gy dose (P<0.002). There was a trend of reduction in migration (P<0.0460, P<0.038, P<0.0024, P<0.0002), as well as a decrease in invasiveness (P<0.0525, P<0.0035, P<0.0868, P<0.0310) after exposure to 0.5 Gy, 1 Gy, 2 Gy and 4 Gy of C-ions.ConclusionsThe presence of irradiated fibroblasts affected the invasiveness capability of pancreatic cancer cells, probably by the reciprocal release of soluble factors whose production is differently modulated after high or low-LET radiation. Understanding the effects of irradiation on the metastatic potential of pancreatic cancer cells is of utmost importance for improving the outcome and tailoring the therapeutic approach. This challenging scenario requires a continuous and multidisciplinary approach that involves clinicians together with researcher experts in oncological and radiation treatment. In the last years, including preclinical experiences in a multidisciplinary approach has proved to be a winning strategy in clinical oncological research.https://www.frontiersin.org/articles/10.3389/fonc.2022.1003494/fulltumor microenvironmentpancreatic cancerlow-LEThigh-LETcarbon ionsmigration
spellingShingle Alexandra Charalampopoulou
Amelia Barcellini
Mario Ciocca
Riccardo Di Liberto
Francesca Pasi
Marco Giuseppe Pullia
Ester Orlandi
Angelica Facoetti
Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
Frontiers in Oncology
tumor microenvironment
pancreatic cancer
low-LET
high-LET
carbon ions
migration
title Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
title_full Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
title_fullStr Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
title_full_unstemmed Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
title_short Factors released by low and high-LET irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
title_sort factors released by low and high let irradiated fibroblasts modulate migration and invasiveness of pancreatic cancer cells
topic tumor microenvironment
pancreatic cancer
low-LET
high-LET
carbon ions
migration
url https://www.frontiersin.org/articles/10.3389/fonc.2022.1003494/full
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