Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model

Inflammation is associated with an increased risk of developing various cancers in both animals and humans, primarily solid tumors but also myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). Multi-walled carbon nanotubes (MWCNTs), a type of carbon...

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Main Authors: Qingqing Wang, Jingdan Han, Mujia Wei, Huikai Miao, Min Zhang, Biao Wu, Yao Chen, Yanwen Zheng, Robert Peter Gale, Bin Yin
Format: Article
Language:English
Published: MDPI AG 2024-09-01
Series:Toxics
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Online Access:https://www.mdpi.com/2305-6304/12/9/646
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author Qingqing Wang
Jingdan Han
Mujia Wei
Huikai Miao
Min Zhang
Biao Wu
Yao Chen
Yanwen Zheng
Robert Peter Gale
Bin Yin
author_facet Qingqing Wang
Jingdan Han
Mujia Wei
Huikai Miao
Min Zhang
Biao Wu
Yao Chen
Yanwen Zheng
Robert Peter Gale
Bin Yin
author_sort Qingqing Wang
collection DOAJ
description Inflammation is associated with an increased risk of developing various cancers in both animals and humans, primarily solid tumors but also myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). Multi-walled carbon nanotubes (MWCNTs), a type of carbon nanotubes (CNTs) increasingly used in medical research and other fields, are leading to a rising human exposure. Our study demonstrated that exposing mice to MWCNTs accelerated the progression of spontaneous MOL4070LTR virus-induced leukemia. Additionally, similar exposures elevated pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α and induced reactive oxygen species (ROS) in a murine macrophage cell line. These effects were significantly reduced in immunodeficient mice and when mice were treated with methoxypolyethylene glycol amine (PEG)-modified MWCNTs. These findings underscore the necessity of evaluating the safety of MWCNTs, particularly for those with hematologic cancers.
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institution Kabale University
issn 2305-6304
language English
publishDate 2024-09-01
publisher MDPI AG
record_format Article
series Toxics
spelling doaj-art-1bc448f41851400f823276edc894125a2025-01-03T02:57:14ZengMDPI AGToxics2305-63042024-09-0112964610.3390/toxics12090646Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse ModelQingqing Wang0Jingdan Han1Mujia Wei2Huikai Miao3Min Zhang4Biao Wu5Yao Chen6Yanwen Zheng7Robert Peter Gale8Bin Yin9Clinical Medical Research Center, The Affiliated Wuxi No.2 People’s Hospital of Nanjing Medical University, Wuxi 214002, ChinaClinical Medical Research Center, The Affiliated Wuxi No.2 People’s Hospital of Nanjing Medical University, Wuxi 214002, ChinaClinical Medical Research Center, The Affiliated Wuxi No.2 People’s Hospital of Nanjing Medical University, Wuxi 214002, ChinaDepartment of Laboratory Medicine, Jiangnan University Medical Center, Wuxi 214002, ChinaDepartment of Laboratory Medicine, Jiangnan University Medical Center, Wuxi 214002, ChinaDepartment of Laboratory Medicine, Jiangnan University Medical Center, Wuxi 214002, ChinaDepartment of Laboratory Medicine, Jiangnan University Medical Center, Wuxi 214002, ChinaCyrus Tang Hematology Center, Jiangsu Institute of Hematology, The First Affiliated Hospital, Soochow University, Suzhou 215123, ChinaHaematology Research Centre, Department of Immunology and Inflammation, Imperial College London, London SW7 2AZ, UKClinical Medical Research Center, The Affiliated Wuxi No.2 People’s Hospital of Nanjing Medical University, Wuxi 214002, ChinaInflammation is associated with an increased risk of developing various cancers in both animals and humans, primarily solid tumors but also myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). Multi-walled carbon nanotubes (MWCNTs), a type of carbon nanotubes (CNTs) increasingly used in medical research and other fields, are leading to a rising human exposure. Our study demonstrated that exposing mice to MWCNTs accelerated the progression of spontaneous MOL4070LTR virus-induced leukemia. Additionally, similar exposures elevated pro-inflammatory cytokines such as interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α and induced reactive oxygen species (ROS) in a murine macrophage cell line. These effects were significantly reduced in immunodeficient mice and when mice were treated with methoxypolyethylene glycol amine (PEG)-modified MWCNTs. These findings underscore the necessity of evaluating the safety of MWCNTs, particularly for those with hematologic cancers.https://www.mdpi.com/2305-6304/12/9/646multi-walled carbon nanotubesleukemiaPEGinflammationMOL4070LTR
spellingShingle Qingqing Wang
Jingdan Han
Mujia Wei
Huikai Miao
Min Zhang
Biao Wu
Yao Chen
Yanwen Zheng
Robert Peter Gale
Bin Yin
Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
Toxics
multi-walled carbon nanotubes
leukemia
PEG
inflammation
MOL4070LTR
title Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
title_full Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
title_fullStr Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
title_full_unstemmed Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
title_short Multi-Walled Carbon Nanotubes Accelerate Leukaemia Development in a Mouse Model
title_sort multi walled carbon nanotubes accelerate leukaemia development in a mouse model
topic multi-walled carbon nanotubes
leukemia
PEG
inflammation
MOL4070LTR
url https://www.mdpi.com/2305-6304/12/9/646
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