Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor

Abstract Background Overwhelming Fe accumulation in tumor arouses strong oxidative stress. To benefit the cancer patients, Fe(II) delivered by carbon nanoparticles-Fe(II) complex (CNSI-Fe) should be visualized to ensure the successful intratumoral injection and the antitumor mechanisms should be inv...

Full description

Bibliographic Details
Main Authors: Ping Xie, Yuanfang Huang, Kexin Tang, Xian Wu, Cheng Zeng, Sheng-Tao Yang, Xiaohai Tang
Format: Article
Language:English
Published: BMC 2023-04-01
Series:Cancer Nanotechnology
Subjects:
Online Access:https://doi.org/10.1186/s12645-023-00196-5
_version_ 1797841156034265088
author Ping Xie
Yuanfang Huang
Kexin Tang
Xian Wu
Cheng Zeng
Sheng-Tao Yang
Xiaohai Tang
author_facet Ping Xie
Yuanfang Huang
Kexin Tang
Xian Wu
Cheng Zeng
Sheng-Tao Yang
Xiaohai Tang
author_sort Ping Xie
collection DOAJ
description Abstract Background Overwhelming Fe accumulation in tumor arouses strong oxidative stress. To benefit the cancer patients, Fe(II) delivered by carbon nanoparticles-Fe(II) complex (CNSI-Fe) should be visualized to ensure the successful intratumoral injection and the antitumor mechanisms should be investigated at molecular level. Results Intracellular Fe accumulations associating with the uptakes of CNSI-Fe were observed both in vitro and in vivo. The retention of Fe(II) in tumor over 72 h was visualized by magnetic resonance imaging. CNSI-Fe inhibited the tumor growth and expanded the lifespan of colonic tumor-bearing mice. The antitumor activity of CNSI-Fe was attributed to the increases of OH radicals and the oxidative stress in tumor cells, which resulted in cell apoptosis and ferroptosis. The transcriptome analyses confirmed the changes of ferroptosis and inflammation signaling pathways by CNSI-Fe treatment. The low toxicity of CNSI-Fe was indicated by the serum biochemistry, hematology, and histopathology. Conclusion CNSI-Fe induced the efficient apoptosis and ferroptosis of colonic tumor for cancer therapy. Our results would benefit the clinical applications of CNSI-Fe and stimulate great interest in the nanomedicine.
first_indexed 2024-04-09T16:26:30Z
format Article
id doaj.art-881d148168d7441fa8f6efd113dbf175
institution Directory Open Access Journal
issn 1868-6958
1868-6966
language English
last_indexed 2024-04-09T16:26:30Z
publishDate 2023-04-01
publisher BMC
record_format Article
series Cancer Nanotechnology
spelling doaj.art-881d148168d7441fa8f6efd113dbf1752023-04-23T11:09:35ZengBMCCancer Nanotechnology1868-69581868-69662023-04-0114111610.1186/s12645-023-00196-5Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumorPing Xie0Yuanfang Huang1Kexin Tang2Xian Wu3Cheng Zeng4Sheng-Tao Yang5Xiaohai Tang6State Key Laboratory of Oral Diseases, West China, College of Stomatology, Sichuan UniversitySichuan Enray Pharmaceutical Sciences CompanySichuan Enray Pharmaceutical Sciences CompanyKey Laboratory of Pollution Control Chemistry and Environmental Functional Materials for Qinghai-Tibet Plateau of the National Ethnic Affairs Commission, School of Chemistry and Environment, Southwest Minzu UniversitySichuan Enray Pharmaceutical Sciences CompanyKey Laboratory of Pollution Control Chemistry and Environmental Functional Materials for Qinghai-Tibet Plateau of the National Ethnic Affairs Commission, School of Chemistry and Environment, Southwest Minzu UniversitySichuan Enray Pharmaceutical Sciences CompanyAbstract Background Overwhelming Fe accumulation in tumor arouses strong oxidative stress. To benefit the cancer patients, Fe(II) delivered by carbon nanoparticles-Fe(II) complex (CNSI-Fe) should be visualized to ensure the successful intratumoral injection and the antitumor mechanisms should be investigated at molecular level. Results Intracellular Fe accumulations associating with the uptakes of CNSI-Fe were observed both in vitro and in vivo. The retention of Fe(II) in tumor over 72 h was visualized by magnetic resonance imaging. CNSI-Fe inhibited the tumor growth and expanded the lifespan of colonic tumor-bearing mice. The antitumor activity of CNSI-Fe was attributed to the increases of OH radicals and the oxidative stress in tumor cells, which resulted in cell apoptosis and ferroptosis. The transcriptome analyses confirmed the changes of ferroptosis and inflammation signaling pathways by CNSI-Fe treatment. The low toxicity of CNSI-Fe was indicated by the serum biochemistry, hematology, and histopathology. Conclusion CNSI-Fe induced the efficient apoptosis and ferroptosis of colonic tumor for cancer therapy. Our results would benefit the clinical applications of CNSI-Fe and stimulate great interest in the nanomedicine.https://doi.org/10.1186/s12645-023-00196-5Carbon nanoparticlesFerrous ironAntitumor activityFerroptosisMagnetic resonance imaging
spellingShingle Ping Xie
Yuanfang Huang
Kexin Tang
Xian Wu
Cheng Zeng
Sheng-Tao Yang
Xiaohai Tang
Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
Cancer Nanotechnology
Carbon nanoparticles
Ferrous iron
Antitumor activity
Ferroptosis
Magnetic resonance imaging
title Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
title_full Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
title_fullStr Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
title_full_unstemmed Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
title_short Carbon nanoparticles-Fe(II) complex for efficient theranostics of xenografted colonic tumor
title_sort carbon nanoparticles fe ii complex for efficient theranostics of xenografted colonic tumor
topic Carbon nanoparticles
Ferrous iron
Antitumor activity
Ferroptosis
Magnetic resonance imaging
url https://doi.org/10.1186/s12645-023-00196-5
work_keys_str_mv AT pingxie carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT yuanfanghuang carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT kexintang carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT xianwu carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT chengzeng carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT shengtaoyang carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor
AT xiaohaitang carbonnanoparticlesfeiicomplexforefficienttheranosticsofxenograftedcolonictumor