Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma

Vascular-targeted PDT (vPDT) has produced promising results in the treatment of many cancers, including drug-resistant ones, but little is known about its efficacy in lymphoma. Unfortunately, the lack of a specific therapeutic target and a hypoxic microenvironment for lymphoma jeopardizes the effica...

Full description

Bibliographic Details
Main Authors: Ziying Li, Yanxue Yin, Weiwei Jin, Bo Zhang, Han Yan, Heng Mei, Huafang Wang, Tao Guo, Wei Shi, Yu Hu
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2020.524712/full
_version_ 1818116143823454208
author Ziying Li
Ziying Li
Yanxue Yin
Yanxue Yin
Weiwei Jin
Bo Zhang
Bo Zhang
Bo Zhang
Han Yan
Han Yan
Heng Mei
Heng Mei
Huafang Wang
Huafang Wang
Tao Guo
Tao Guo
Wei Shi
Wei Shi
Yu Hu
Yu Hu
author_facet Ziying Li
Ziying Li
Yanxue Yin
Yanxue Yin
Weiwei Jin
Bo Zhang
Bo Zhang
Bo Zhang
Han Yan
Han Yan
Heng Mei
Heng Mei
Huafang Wang
Huafang Wang
Tao Guo
Tao Guo
Wei Shi
Wei Shi
Yu Hu
Yu Hu
author_sort Ziying Li
collection DOAJ
description Vascular-targeted PDT (vPDT) has produced promising results in the treatment of many cancers, including drug-resistant ones, but little is known about its efficacy in lymphoma. Unfortunately, the lack of a specific therapeutic target and a hypoxic microenvironment for lymphoma jeopardizes the efficacy of vPDT severely. In this study, we designed a lymphoma tissue factor-targeted “O2-evolving” strategy combining PDT with catalase and HMME-encapsulated, EGFP-EGF1-modified PEG-PLGA nanoparticles (CENPs) to boost PDT efficiency; this combination takes advantage of the low oxygen tension of lymphoma. In our results, CENPs accumulated effectively in the vascular lymphoma in vivo and in vitro, and this accumulation increased further with PDT treatment. Per positron emission tomography imaging, combining CENPs with PDT inhibited lymphoma glucose metabolism significantly. The expression of hypoxia-inducible factor (HIF)-1α in the entrapped catalase groups reduced markedly. These data show that the combined administration of PDT and CENPs can prompt tissue factor-cascade-targeted and self-supply of oxygen and that it has a good therapeutic effect on malignant lymphoma.
first_indexed 2024-12-11T04:17:50Z
format Article
id doaj.art-9050cc58e4914e1795f71ff6fa6115be
institution Directory Open Access Journal
issn 2234-943X
language English
last_indexed 2024-12-11T04:17:50Z
publishDate 2020-11-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Oncology
spelling doaj.art-9050cc58e4914e1795f71ff6fa6115be2022-12-22T01:21:12ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2020-11-011010.3389/fonc.2020.524712524712Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant LymphomaZiying Li0Ziying Li1Yanxue Yin2Yanxue Yin3Weiwei Jin4Bo Zhang5Bo Zhang6Bo Zhang7Han Yan8Han Yan9Heng Mei10Heng Mei11Huafang Wang12Huafang Wang13Tao Guo14Tao Guo15Wei Shi16Wei Shi17Yu Hu18Yu Hu19Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaDepartment of Cardiovascular, Optical Valley School District, Hubei Province Academy of Traditional Chinese Medicine, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaDepartment of Systems Biology, National Cancer Institute Comprehensive Cancer Center, Beckman Research Institute, City of Hope, Monrovia, CA, United StatesInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaInstitute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaTargeted Biotherapy Key Laboratory of Ministry of Education, Wuhan, ChinaVascular-targeted PDT (vPDT) has produced promising results in the treatment of many cancers, including drug-resistant ones, but little is known about its efficacy in lymphoma. Unfortunately, the lack of a specific therapeutic target and a hypoxic microenvironment for lymphoma jeopardizes the efficacy of vPDT severely. In this study, we designed a lymphoma tissue factor-targeted “O2-evolving” strategy combining PDT with catalase and HMME-encapsulated, EGFP-EGF1-modified PEG-PLGA nanoparticles (CENPs) to boost PDT efficiency; this combination takes advantage of the low oxygen tension of lymphoma. In our results, CENPs accumulated effectively in the vascular lymphoma in vivo and in vitro, and this accumulation increased further with PDT treatment. Per positron emission tomography imaging, combining CENPs with PDT inhibited lymphoma glucose metabolism significantly. The expression of hypoxia-inducible factor (HIF)-1α in the entrapped catalase groups reduced markedly. These data show that the combined administration of PDT and CENPs can prompt tissue factor-cascade-targeted and self-supply of oxygen and that it has a good therapeutic effect on malignant lymphoma.https://www.frontiersin.org/articles/10.3389/fonc.2020.524712/fullcatalasephotodynamic therapytissue factornanoparticlesEGFP-EGF1protein
spellingShingle Ziying Li
Ziying Li
Yanxue Yin
Yanxue Yin
Weiwei Jin
Bo Zhang
Bo Zhang
Bo Zhang
Han Yan
Han Yan
Heng Mei
Heng Mei
Huafang Wang
Huafang Wang
Tao Guo
Tao Guo
Wei Shi
Wei Shi
Yu Hu
Yu Hu
Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
Frontiers in Oncology
catalase
photodynamic therapy
tissue factor
nanoparticles
EGFP-EGF1protein
title Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
title_full Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
title_fullStr Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
title_full_unstemmed Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
title_short Tissue Factor-Targeted “O2-Evolving” Nanoparticles for Photodynamic Therapy in Malignant Lymphoma
title_sort tissue factor targeted o2 evolving nanoparticles for photodynamic therapy in malignant lymphoma
topic catalase
photodynamic therapy
tissue factor
nanoparticles
EGFP-EGF1protein
url https://www.frontiersin.org/articles/10.3389/fonc.2020.524712/full
work_keys_str_mv AT ziyingli tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT ziyingli tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT yanxueyin tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT yanxueyin tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT weiweijin tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT bozhang tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT bozhang tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT bozhang tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT hanyan tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT hanyan tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT hengmei tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT hengmei tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT huafangwang tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT huafangwang tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT taoguo tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT taoguo tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT weishi tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT weishi tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT yuhu tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma
AT yuhu tissuefactortargetedo2evolvingnanoparticlesforphotodynamictherapyinmalignantlymphoma