Cargando…

“Locked” cancer cells are more sensitive to chemotherapy

The treatment of metastatic cancer is a great challenging issue throughout the world. Conventional chemotherapy can kill the cancer cells and, whereas, would exacerbate the metastasis and induce drug resistance. Here, a new combinatorial treatment strategy of metastatic cancer was probed via subsequ...

Descripción completa

Detalles Bibliográficos
Autores principales: Lyu, Yaqi, Xiao, Qingqing, Li, Yi, Wu, Yubing, He, Wei, Yin, Lifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584094/
https://www.ncbi.nlm.nih.gov/pubmed/31249880
http://dx.doi.org/10.1002/btm2.10130
_version_ 1783428474909753344
author Lyu, Yaqi
Xiao, Qingqing
Li, Yi
Wu, Yubing
He, Wei
Yin, Lifang
author_facet Lyu, Yaqi
Xiao, Qingqing
Li, Yi
Wu, Yubing
He, Wei
Yin, Lifang
author_sort Lyu, Yaqi
collection PubMed
description The treatment of metastatic cancer is a great challenging issue throughout the world. Conventional chemotherapy can kill the cancer cells and, whereas, would exacerbate the metastasis and induce drug resistance. Here, a new combinatorial treatment strategy of metastatic cancer was probed via subsequentially dosing dual nanomedicines, marimastat‐loaded thermosensitive liposomes (MATT‐LTSLs) and paclitaxel nanocrystals (PTX‐Ns), via intravenous and intratumoral injection. First, the metastasis was blocked and cancer cells were locked in the tumor microenvironment (TME) by delivering the matrix metalloproteinase (MMP) inhibitor, MATT, to the tumor with LTSLs, downregulating the MMPs by threefold and reducing the degradation of the extracellular matrix. And then, the “locked” cancer cells were efficiently killed via intratumoral injection of the other cytotoxic nanomedicine, PTX‐Ns, along with no metastasis and 100% inhibition of tumor growth. This work highlights the importance of the TME's integrity in the chemotherapy duration. We believe this is a generalized strategy for cancer treatment and has potential guidance for the clinical administration.
format Online
Article
Text
id pubmed-6584094
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-65840942019-06-27 “Locked” cancer cells are more sensitive to chemotherapy Lyu, Yaqi Xiao, Qingqing Li, Yi Wu, Yubing He, Wei Yin, Lifang Bioeng Transl Med Research Reports The treatment of metastatic cancer is a great challenging issue throughout the world. Conventional chemotherapy can kill the cancer cells and, whereas, would exacerbate the metastasis and induce drug resistance. Here, a new combinatorial treatment strategy of metastatic cancer was probed via subsequentially dosing dual nanomedicines, marimastat‐loaded thermosensitive liposomes (MATT‐LTSLs) and paclitaxel nanocrystals (PTX‐Ns), via intravenous and intratumoral injection. First, the metastasis was blocked and cancer cells were locked in the tumor microenvironment (TME) by delivering the matrix metalloproteinase (MMP) inhibitor, MATT, to the tumor with LTSLs, downregulating the MMPs by threefold and reducing the degradation of the extracellular matrix. And then, the “locked” cancer cells were efficiently killed via intratumoral injection of the other cytotoxic nanomedicine, PTX‐Ns, along with no metastasis and 100% inhibition of tumor growth. This work highlights the importance of the TME's integrity in the chemotherapy duration. We believe this is a generalized strategy for cancer treatment and has potential guidance for the clinical administration. John Wiley & Sons, Inc. 2019-06-10 /pmc/articles/PMC6584094/ /pubmed/31249880 http://dx.doi.org/10.1002/btm2.10130 Text en © 2019 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Lyu, Yaqi
Xiao, Qingqing
Li, Yi
Wu, Yubing
He, Wei
Yin, Lifang
“Locked” cancer cells are more sensitive to chemotherapy
title “Locked” cancer cells are more sensitive to chemotherapy
title_full “Locked” cancer cells are more sensitive to chemotherapy
title_fullStr “Locked” cancer cells are more sensitive to chemotherapy
title_full_unstemmed “Locked” cancer cells are more sensitive to chemotherapy
title_short “Locked” cancer cells are more sensitive to chemotherapy
title_sort “locked” cancer cells are more sensitive to chemotherapy
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584094/
https://www.ncbi.nlm.nih.gov/pubmed/31249880
http://dx.doi.org/10.1002/btm2.10130
work_keys_str_mv AT lyuyaqi lockedcancercellsaremoresensitivetochemotherapy
AT xiaoqingqing lockedcancercellsaremoresensitivetochemotherapy
AT liyi lockedcancercellsaremoresensitivetochemotherapy
AT wuyubing lockedcancercellsaremoresensitivetochemotherapy
AT hewei lockedcancercellsaremoresensitivetochemotherapy
AT yinlifang lockedcancercellsaremoresensitivetochemotherapy