The breast tumor microenvironment: role in cancer development, progression and response to therapy
- PMID: 29424261
- DOI: 10.1080/14737159.2018.1439382
The breast tumor microenvironment: role in cancer development, progression and response to therapy
Abstract
Numerous clinical and pre-clinical studies have provided ample evidence supporting that the tumor microenvironment plays a significant role during breast cancer development, progression and in determining the therapeutic response. Areas covered: This review focuses on the evolving concept of the microenvironment as the critical participant in each step of the multi-stage process of malignant progression. Currently, only a small number of molecules form part of routine molecular diagnostics in breast caner, but microenvironment-derived biomarkers are potential additions to existing predictive and prognostic marker panels. The authors discuss the dependency of the breast tumor cells on different components of the microenvironment for their survival, dissemination, dormancy and establishment in secondary sites to form overt metastasis, as well as the potential as a therapeutic target to improve breast cancer outcome. Expert commentary: Despite the importance in the development of breast cancer, the contribution of the microenvironment is not considered in routine diagnostic testing or informing therapeutic decisions. However, introduction of immunotherapy will increasingly require patient selection based on the stromal composition of the primary breast tumor. Better understanding of the role of specific microenvironment-derived molecules is likely to inform personalized therapy, leading to improved patient outcome.
Keywords: Breast cancer; bone; bone metastases; bone targeted agents; microenvironment.
Similar articles
-
Molecular insights into prostate cancer progression: the missing link of tumor microenvironment.J Urol. 2005 Jan;173(1):10-20. doi: 10.1097/01.ju.0000141582.15218.10. J Urol. 2005. PMID: 15592017 Review.
-
Bone Metastasis of Breast Cancer.Adv Exp Med Biol. 2019;1152:105-129. doi: 10.1007/978-3-030-20301-6_7. Adv Exp Med Biol. 2019. PMID: 31456182 Review.
-
Granulocytic immune infiltrates are essential for the efficient formation of breast cancer liver metastases.Breast Cancer Res. 2015 Mar 27;17(1):45. doi: 10.1186/s13058-015-0558-3. Breast Cancer Res. 2015. PMID: 25882816 Free PMC article.
-
Pathological Crosstalk between Metastatic Breast Cancer Cells and the Bone Microenvironment.Biomolecules. 2020 Feb 19;10(2):337. doi: 10.3390/biom10020337. Biomolecules. 2020. PMID: 32092997 Free PMC article. Review.
-
The influence of the pre-metastatic niche on breast cancer metastasis.Cancer Lett. 2016 Sep 28;380(1):281-8. doi: 10.1016/j.canlet.2015.11.009. Epub 2015 Nov 11. Cancer Lett. 2016. PMID: 26577808 Review.
Cited by
-
PUF60 accelerates the progression of breast cancer through downregulation of PTEN expression.Cancer Manag Res. 2019 Jan 17;11:821-830. doi: 10.2147/CMAR.S180242. eCollection 2019. Cancer Manag Res. 2019. PMID: 30697074 Free PMC article.
-
Contemporary evaluation of estrogen receptor and progesterone receptor expression in breast cancer-associated stroma.Breast Cancer Res Treat. 2022 Dec;196(3):453-461. doi: 10.1007/s10549-022-06754-6. Epub 2022 Oct 8. Breast Cancer Res Treat. 2022. PMID: 36208382
-
Preclinical PET Imaging of Granzyme B Shows Promotion of Immunological Response Following Combination Paclitaxel and Immune Checkpoint Inhibition in Triple Negative Breast Cancer.Pharmaceutics. 2022 Feb 18;14(2):440. doi: 10.3390/pharmaceutics14020440. Pharmaceutics. 2022. PMID: 35214172 Free PMC article.
-
The pleiotropic roles of adipocyte secretome in remodeling breast cancer.J Exp Clin Cancer Res. 2022 Jun 14;41(1):203. doi: 10.1186/s13046-022-02408-z. J Exp Clin Cancer Res. 2022. PMID: 35701840 Free PMC article. Review.
-
ADSCs stimulated by resistin promote breast cancer cell malignancy via CXCL5 in a breast cancer coculture model.Sci Rep. 2022 Sep 14;12(1):15437. doi: 10.1038/s41598-022-19290-6. Sci Rep. 2022. PMID: 36104403 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical