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Yi-Wen Shen
Researcher at Shanghai University
Publications - Â 11
Citations - Â 244
Yi-Wen Shen is an academic researcher from Shanghai University. The author has contributed to research in topics: Tumor microenvironment & Cancer. The author has an hindex of 4, co-authored 10 publications receiving 43 citations.
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Journal ArticleDOI
Mesoporous silica nanoparticles: facile surface functionalization and versatile biomedical applications in oncology
Rui Huang,Yi-Wen Shen,Ying-Yun Guan,Yi-Xin Jiang,Ye Wu,Khalid Rahman,Li-Jun Zhang,Hai-Jun Liu,Xin Luan +8 more
TL;DR: This review summarises the different synthetic methods for the preparation of well-ordered MSNs with tunable pore volume as well as the approaches of drugs loading, especially highlighting the facile surface functionalization for various purposes and versatile biomedical applications in oncology.
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The peptide PROTAC modality: a novel strategy for targeted protein ubiquitination.
Jinmei Jin,Ye Wu,Jin-Jiao Chen,Jin-Jiao Chen,Yi-Wen Shen,Li-Jun Zhang,Hong Zhang,Lili Chen,Hebao Yuan,Hong-Zhuan Chen,Hong-Zhuan Chen,Weidong Zhang,Xin Luan +12 more
TL;DR: It is highlighted that p-PROTAC combined with cell-penetrating peptides, constrained conformation technique, and targeted delivery systems could be the future efforts for potential translational research.
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Targeting CTGF in Cancer: An Emerging Therapeutic Opportunity
TL;DR: In this article, the authors comprehensively discuss the expression of CTGF and its regulation, oncogenic role, clinical relevance, targeting strategies, and therapeutic agents and propose that CTGF is a promising cancer therapeutic target that could potentially improve the clinical outcomes of cancer patients.
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Cytotoxic and antitumor peptides as novel chemotherapeutics.
Xin Luan,Ye Wu,Yi-Wen Shen,Hong Zhang,Yu-Dong Zhou,Yu-Dong Zhou,Hong-Zhuan Chen,Dale G. Nagle,Dale G. Nagle,Weidong Zhang,Weidong Zhang +10 more
TL;DR: In-depth review of several peptides provides examples for how this novel strategy can lead to the improved anti-tumor effects, with a particular focus on future directions for interdisciplinary research.
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Emerging protein degradation strategies: expanding the scope to extracellular and membrane proteins.
Jiayi Lin,Jinmei Jin,Yi-Wen Shen,Li-Jun Zhang,Gang Gong,Huiting Bian,Hong-Zhuan Chen,Dale G. Nagle,Ye Wu,Weidong Zhang,Weidong Zhang,Xin Luan +11 more
Abstract: Classic small molecule inhibitors that directly target pathogenic proteins typically rely on the accessible binding sites to achieve prolonged occupancy and influence protein functions. The emerging targeted protein degradation (TPD) strategies exemplified by PROteolysis TArgeting Chimeras (PROTACs) are revolutionizing conventional drug discovery modality to target proteins of interest (POIs) that were categorized as "undruggable" before, however, these strategies are limited within intracellular POIs. The novel new degrader technologies such as LYsosome-TArgeting Chimaeras (LYTACs) and Antibody-based PROTACs (AbTACs) have been successfully developed to expand the scope of TPD to extracellular and membrane proteins, fulfilling huge unmet medical needs. Here, we systematically review the currently viable protein degradation strategies, emphasize that LYTACs and AbTACs turn a new avenue for the development of TPD, and highlight the potential challenges and directions in this vibrant field.