Tumor microenvironment complexity and therapeutic implications at a glance

被引:1354
作者
Baghba, Roghayyeh [1 ,2 ]
Roshangar, Leila [3 ]
Jahanban-Esfahlan, Rana [2 ]
Seidi, Khaled [4 ,5 ]
Ebrahimi-Kalan, Abbas [6 ]
Jaymand, Mehdi [7 ]
Kolahian, Saeed [8 ]
Javaheri, Tahereh [9 ]
Zare, Peyman [10 ,11 ]
机构
[1] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Sch Adv Med Sci, Dept Med Biotechnol, Tabriz, Iran
[3] Tabriz Univ Med Sci, Stem Cell Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[5] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[6] Tabriz Univ Med Sci, Sch Adv Med Sci, Dept Neurosci & Cognit, Tabriz, Iran
[7] Kermanshah Univ Med Sci, Nano Drug Delivery Res Ctr, Hlth Technol Inst, Kermanshah, Iran
[8] Univ Hosp Tuebingen, Dept Expt & Clin Pharmacol & Pharmacogen, Tubingen, Germany
[9] Boston Univ, Metropolitan Coll, Hlth Informat Lab, Boston, MA 02215 USA
[10] Polish Acad Sci, Dioscuri Ctr Chromatin Biol & Epigen, Nencki Inst Expt Biol, Warsaw, Poland
[11] Cardinal Stefan VVyszynski Univ Warsaw, Fac Med, PL-01938 Warsaw, Poland
关键词
Cancer cell interactions; Tumor microenvironment; Extracellular matrix; Cancer therapy; Stroma cell; Circulating tumor cells; Cell-free DNA; Apoptotic bodies; Exosome; Horizontal transfer; Cancer models; CANCER-ASSOCIATED FIBROBLASTS; CELL-FREE DNA; CIRCULATING NUCLEIC-ACIDS; EXTRACELLULAR-MATRIX; ENDOTHELIAL-CELLS; STROMAL FIBROBLASTS; VASCULAR PERICYTES; PANCREATIC-CANCER; OXIDATIVE STRESS; DRUG-RESISTANCE;
D O I
10.1186/s12964-020-0530-4
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The dynamic interactions of cancer cells with their microenvironment consisting of stromal cells (cellular part) and extracellular matrix (ECM) components (non-cellular) is essential to stimulate the heterogeneity of cancer cell, clonal evolution and to increase the multidrug resistance ending in cancer cell progression and metastasis. The reciprocal cell-cell/ECM interaction and tumor cell hijacking of non-malignant cells force stromal cells to lose their function and acquire new phenotypes that promote development and invasion of tumor cells. Understanding the underlying cellular and molecular mechanisms governing these interactions can be used as a novel strategy to indirectly disrupt cancer cell interplay and contribute to the development of efficient and safe therapeutic strategies to fight cancer. Furthermore, the tumor-derived circulating materials can also be used as cancer diagnostic tools to precisely predict and monitor the outcome of therapy. This review evaluates such potentials in various advanced cancer models, with a focus on 3D systems as well as lab-on-chip devices.
引用
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页数:19
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