Research output: Contribution to journal › Review article › peer-review
Mutual influence of malignant cells and cellular microenvironment : prospects for manipulating tumour microenvironment with nanomaterials. / Malkova, Anna M.; Ageev, Sergei V.; Abdelhalim, Abdelsattar O.E.; Molchanov, Oleg E.; Maistrenko, Dmitrii N.; Semenov, Konstantin N.; Sharoyko, Vladimir V.
In: Cellular Therapy and Transplantation , Vol. 10, No. 3-4, 12.2021, p. 8-18.Research output: Contribution to journal › Review article › peer-review
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TY - JOUR
T1 - Mutual influence of malignant cells and cellular microenvironment
T2 - prospects for manipulating tumour microenvironment with nanomaterials
AU - Malkova, Anna M.
AU - Ageev, Sergei V.
AU - Abdelhalim, Abdelsattar O.E.
AU - Molchanov, Oleg E.
AU - Maistrenko, Dmitrii N.
AU - Semenov, Konstantin N.
AU - Sharoyko, Vladimir V.
N1 - Publisher Copyright: © 2021, Universitatsklinikum Hamburg - Eppendorf. All rights reserved.
PY - 2021/12
Y1 - 2021/12
N2 - Development and progression of neoplasia occurs in par-allel with changes in the surrounding stroma. Cancer cells may functionally reshape their microenvironment by secreting various cytokines, chemokines and generation of acidic medium. These factors contribute to differentiation of immune cells into immunosuppressive phenotype, stimulate the synthesis of a number of amino acid me-tabolism enzymes, growth factors, adhesion molecules, which promote invasion, angiogenesis and metastasis, and also reduce efficiency of anticancer drugs and radia-tion therapy. To increase effectiveness of the chemother-apy, multitargeted carbon nanomaterials may be applied. In particular, nanomaterials based on modified graphene make it possible to create multicomponent therapeutic constructs, including macromolecules, polymers, and effector agents. Initial experiments with unmodified graphenes demonstrated their toxicity associated with their accumulation in parenchymal organs and initiation of inflammatory processes. In the past few years, a series of works has been published in which the possibility of reducing the toxicity of graphene oxide through function-alisation has been demonstrated. This review summaris-es the experimental data on the creation of covalent and non-covalent conjugates based on graphene oxide and demonstrates their in vitro efficacy on various tumour cell lines. Separately, there are few data on the effect of nanomaterials based on graphene oxide on the tumour microenvironment.
AB - Development and progression of neoplasia occurs in par-allel with changes in the surrounding stroma. Cancer cells may functionally reshape their microenvironment by secreting various cytokines, chemokines and generation of acidic medium. These factors contribute to differentiation of immune cells into immunosuppressive phenotype, stimulate the synthesis of a number of amino acid me-tabolism enzymes, growth factors, adhesion molecules, which promote invasion, angiogenesis and metastasis, and also reduce efficiency of anticancer drugs and radia-tion therapy. To increase effectiveness of the chemother-apy, multitargeted carbon nanomaterials may be applied. In particular, nanomaterials based on modified graphene make it possible to create multicomponent therapeutic constructs, including macromolecules, polymers, and effector agents. Initial experiments with unmodified graphenes demonstrated their toxicity associated with their accumulation in parenchymal organs and initiation of inflammatory processes. In the past few years, a series of works has been published in which the possibility of reducing the toxicity of graphene oxide through function-alisation has been demonstrated. This review summaris-es the experimental data on the creation of covalent and non-covalent conjugates based on graphene oxide and demonstrates their in vitro efficacy on various tumour cell lines. Separately, there are few data on the effect of nanomaterials based on graphene oxide on the tumour microenvironment.
KW - acidosis
KW - carbon nanomaterials
KW - cytokines
KW - immune system
KW - microenvironment
KW - progression
KW - Tumour
UR - http://www.scopus.com/inward/record.url?scp=85126923083&partnerID=8YFLogxK
U2 - 10.18620/ctt-1866-8836-2021-10-3-4-8-18
DO - 10.18620/ctt-1866-8836-2021-10-3-4-8-18
M3 - Review article
AN - SCOPUS:85126923083
VL - 10
SP - 8
EP - 18
JO - Cellular Therapy and Transplantation
JF - Cellular Therapy and Transplantation
SN - 1867-416X
IS - 3-4
ER -
ID: 100131271