Supramolecular Self-Assembly-Facilitated Aggregation of Tumor-Specific Transmembrane Receptors for Signaling Activation and Converting Immunologically Cold to Hot Tumors

© 2021 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 33(2021), 16 vom: 17. Apr., Seite e2008518
1. Verfasser: Li, Jun (VerfasserIn)
Weitere Verfasser: Fang, Yuan, Zhang, Yufan, Wang, Huaimin, Yang, Zhimou, Ding, Dan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2021
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article EphA2 receptors cancer theranostics immunologically cold/hot tumors molecule-targeted anticancer agents supramolecular self-assembling peptides Receptor, EphA2 EC 2.7.10.1 Peptides Antineoplastic Agents
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520 |a Supramolecular self-assembling peptide systems are attracting increasing interest in the field of cancer theranostics. Additionally, transformation of the immunologically cold tumor microenvironment into hot is of great importance for obtaining high antitumor responses for most immunotherapies. However, as far as it is known, there are nearly no studies on self-assembling peptides reported to be able to convert cold to hot tumors. Herein, a self-assembling peptide-based cancer theranostic agent (named DBT-2FFGYSA) is designed and synthesized, which can target tumor-specific transmembrane Eph receptor A2 (EphA2) receptors selectively and make the receptors form large aggregates. Such aggregate formation promotes the cross-phosphorylations among EphA2 receptors, leading to signal transduction of antitumor pathway. As a consequence, DBT-2FFGYSA can not only visualize EphA2 receptors in a fluorescence turn-on manner, but also specifically suppress the EphA2 receptor-overexpressed cancer cell proliferation and tumor growth. What is more, DBT-2FFGYSA also serves as an effective agent to convert immunologically cold tumors to hot by inducing the immunogenic cell death of EphA2 receptor-overexpressed cancer cells and recruiting massive tumor-infiltrating T cells. This study, thus, introduces a new category of agents capable of converting cold to hot tumors by pure supramolecular self-assembly without any aid of known anticancer drugs 
650 4 |a Journal Article 
650 4 |a EphA2 receptors 
650 4 |a cancer theranostics 
650 4 |a immunologically cold/hot tumors 
650 4 |a molecule-targeted anticancer agents 
650 4 |a supramolecular self-assembling peptides 
650 7 |a Receptor, EphA2  |2 NLM 
650 7 |a EC 2.7.10.1  |2 NLM 
650 7 |a Peptides  |2 NLM 
650 7 |a Antineoplastic Agents  |2 NLM 
700 1 |a Fang, Yuan  |e verfasserin  |4 aut 
700 1 |a Zhang, Yufan  |e verfasserin  |4 aut 
700 1 |a Wang, Huaimin  |e verfasserin  |4 aut 
700 1 |a Yang, Zhimou  |e verfasserin  |4 aut 
700 1 |a Ding, Dan  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 33(2021), 16 vom: 17. Apr., Seite e2008518  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnns 
773 1 8 |g volume:33  |g year:2021  |g number:16  |g day:17  |g month:04  |g pages:e2008518 
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