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Review
. 2021 Apr 22:11:650453.
doi: 10.3389/fonc.2021.650453. eCollection 2021.

Extracellular Matrix: Emerging Roles and Potential Therapeutic Targets for Breast Cancer

Yunchun Zhao  1   2 , Xiaoling Zheng  1   2 , Yongquan Zheng  1   2 , Yue Chen  1   2 , Weidong Fei  1   2 , Fengmei Wang  1   2 , Caihong Zheng  1   2
Affiliations
Review

Extracellular Matrix: Emerging Roles and Potential Therapeutic Targets for Breast Cancer

Yunchun Zhao et al. Front Oncol. .

Abstract

Increasing evidence shows that the extracellular matrix (ECM) is an important regulator of breast cancer (BC). The ECM comprises of highly variable and dynamic components. Compared with normal breast tissue under homeostasis, the ECM undergoes many changes in composition and organization during BC progression. Induced ECM proteins, including fibrinogen, fibronectin, hyaluronic acid, and matricellular proteins, have been identified as important components of BC metastatic cells in recent years. These proteins play major roles in BC progression, invasion, and metastasis. Importantly, several specific ECM molecules, receptors, and remodeling enzymes are involved in promoting resistance to therapeutic intervention. Additional analysis of these ECM proteins and their downstream signaling pathways may reveal promising therapeutic targets against BC. These potential drug targets may be combined with new nanoparticle technologies. This review summarizes recent advances in functional nanoparticles that target the ECM to treat BC. Accurate nanomaterials may offer a new approach to BC treatment.

Keywords: breast cancer; extracellular matrix; nanoparticles; remodeling enzymes; therapeutic targets.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Synthesis and characterization of CLG@NCP-PEG NPs. Scheme for the preparation of NCP NPs and CLG-encapsulated CLG@NCP nanoparticles, surface modification, and pH-sensitive degradation. Reproduced with permission from (138).
Figure 2
Figure 2
Synthesis and characterization of Peptide PS/PTX micelles. (A) Scheme of the lock copolymer structural sequence. (B) Peptide-PEG-PLGA conjugate is mixed with PTX and self-assembled into Peptide PS/PTX micelles. (C) Surface-modified peptide PS/PTX micelles and is pH-sensitive and glutathione-sensitive degradation.
See this image and copyright information in PMC

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