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Review
. 2024 Apr 30:14:1389775.
doi: 10.3389/fonc.2024.1389775. eCollection 2024.

Research progress of cell membrane biomimetic nanoparticles for circulating tumor cells

Affiliations
Review

Research progress of cell membrane biomimetic nanoparticles for circulating tumor cells

Yingfeng Zhang et al. Front Oncol. .

Abstract

Early detection of cancer is crucial to reducing fatalities and improving patient outcomes. Metastasis is the first stage of aggressive cancers, often occurring before primary lesions can be seen. It occurs when cancerous cells disseminate to distant, non-malignant organs through the bloodstream, known as circulating tumor cells (CTCs). CTCs, or cancer tumor cells, are valuable indicators for predicting treatment response, metastasis progression, and disease progression. However, they are primarily used for research due to challenges like heterogeneity, separation from blood, and lack of clinical validation. Only a few methods have been approved for clinical use. One area of research is the isolation and identification of CTCs, which could significantly impact early cancer detection and prognosis. Current technologies using whole-blood samples use size, immunoaffinity, and density approaches, along with positive and negative enrichment techniques. Surface modification of nanomaterials is important for effective cancer therapies because it improves their ability to target and reduces interactions with healthy tissues. Consequently, researchers have created biomimetic nanoparticles covered with cell membranes using functional, targeted, and biocompatible coating technology. Nanoparticles with membranes can target specific cells, stay in circulation for longer, and avoid immune responses, which makes them much better at capturing CTCs. This study examines the current opportunities and difficulties associated with using cell membrane-coated nanoparticles as a capture technique for CTCs. In addition, we examine potential future developments in light of the current obstacles and investigate areas that require further research to fully understand its growing clinical possibilities.

Keywords: biomimetic nanoparticles; cell membrane; circulating tumor cells; diagnosis; progress.

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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
(A) Liquid biopsy. (B) CTCs are released from the main tumor and have a direct role in the process of metastasis, as described by Paget’s “seed and soil” hypothesis. (C) Isolation and identification of CTC. (D) A wide variety of cell membrane types have been extensively studied for their ability to encapsulate nanoparticles.
Figure 2
Figure 2
(A) Schematic illustration of the preparation of ethyl cellulose/chitosan microspheres (ECCMs) and their applications in cancer theranostics. (B) Schematic illustration of targeting CTCs and preventing them from forming new pre-metastatic clones through neutrophil-mimicking NPs (NM-NPs) used to deliver an anticancer drug.
Figure 3
Figure 3
(A) An individual CTCs may now be examined to produce proteomic, transcriptomic, and epigenomic data. (B) Epithelial-to-mesenchymal transition of CTCs.
Figure 4
Figure 4
(A) CTCs in the blood microenvironment, and their interaction with neutrophils, platelets, CAFs, and TAMs. CAFs, cancer-associated fibroblasts, TAMs, tumor-associated macrophages. (B) The utility of liquid biopsy during different stages of tumor progression.
Figure 5
Figure 5
(A) Technologies for CTC enrichment based on physical properties. (B) Microfiltration technique for cell separation. (C) Nanotechnology improves cancer detection and diagnosis.
Figure 6
Figure 6
(A) Schematic of the different forms of cell primitives and synthetic materials, respectively, and their potential as building blocks to fabricate cell primitive-based functional materials as newly emerging therapeutic formulations. (B) A schematic diagram of the preparation of membrane-coated biomimetic nanoparticles and their functions. (C) RBC membrane–coated nanoparticles. Cell membrane can be derived from RBCs using hypotonic treatment. (D) Schematic illustration of anti–PD-L1 delivery to primary-tumor resection sites by platelets, where TCR is T-cell receptor, and MHC is the major histocompatibility complex.
Figure 7
Figure 7
(A) Different source immune cells and various types of NPs formed via camouflaging different cell membranes. First, immune cell membranes are isolated from blood or their other sources and then extruded to obtain membrane vesicles. Finally, the vesicles fuse with core NPs to form membrane-camouflaged NPs. (B) Schematic illustration of neutrophils-mimicking nanoparticles loaded with carfilzomib (NM-NP-CFZ) that selectively deplete CTC and their site of colonization. (C) Schematic illustration of PCN@FM for combined tumor therapy.
Figure 8
Figure 8
(A) Tumors parameters implicated in the activation of NK cells. (B) Schematic illustration of the cancer cell membrane camouflaged cascade bioreactor for cancer targeting starvation therapy and PDT. (C) Mesenchymal stem cell membrane–coated growth-factor-loaded nanoparticles for tissue repair. Synthetics MSCs release loaded growth factors to promote tissue repair through cell proliferation, angiogenesis, and remuscularization.
Figure 9
Figure 9
(A) Hybrid RBC-cancer cell membrane–coated hollow copper sulfide NPs for PTT. (B) Steps to synthesize biomimetic immune cell membrane–based nanoplatforms. (C) A schematic diagram of the surface modification methods of RBCMs-based nanomedicine.
Figure 10
Figure 10
(A) Each class of nanoparticle (NP) features multiple subclasses, with some of the most common highlighted here. Each class has numerous broad advantages and disadvantages regarding cargo, delivery and patient response. (B) Common uptake pathways that ultimately determine NP fate within a cell.
Figure 11
Figure 11
(A) Schematic of the synthesis and application of cancer cell membrane–coated gold nanoparticles (CC-AuNPs) and cancer cell membrane–coated upconversion nanoparticles (CC-UCNPs) combined with a novel simultaneous dual-modal imaging platform for guided photothermal therapy (PTT) for cancer. (B) Schematic illustration to show the structure of tumor cell membrane coated, R873 loaded, and mannose modified PLGA NPs (NP-R@M-M), and their functions to induce anti-tumor immunity as a nanovaccine. (C) Fabrication process of leukocyte-mimicking immunomagnetic nanoplatform and general CTCs isolation process in blood samples. (D) Schematic of the preparation of HM-IMBs for high-performance isolation of CTCs.
Figure 12
Figure 12
(A) Illustration of the preparation of HM-Fe3O4@SiO2/Tetra-DNA-Ag2S nanoplatform for the efficient isolation and detection of rare CTCs. (B) Construction of IMS and the procedure of CTC enrichment. (C) Targeted co-delivery of PD-L1 monoclonal antibody and sorafenib to circulating tumor cells via platelet-functionalized nanocarriers. (D) Suppressive mechanism of regulatory T (Treg) cells.

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Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was also funded by project of Science and Technology Research Project of Chongqing Education Commission, KJQN202200462, study on the effect and mechanism of LncRNA RMST and Notch signaling pathway on trophoblast cells.

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