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Yi-Wen Shen

Researcher at Shanghai University

Publications -  11
Citations -  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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Mesoporous silica nanoparticles: facile surface functionalization and versatile biomedical applications in oncology

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.

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.

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.

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.