CXC Chemokine‐Driven Vascular Reprogramming: Modulating Tumor Vasculature to Boost Therapeutic Response
Aberrant tumor vasculature drives hypoxia, immune exclusion, and therapeutic resistance. However, current vascular normalization strategies remain primarily VEGF-centered, relying on morphological and perfusion metrics with limited molecular readouts to monitor vessel function. This highlights the need for alternative frameworks to identify therapeutic windows and enhance vascular-immune strategies. Here, we introduce a chemokine-centered perspective that positions the CXC chemokine network as a dynamic regulator of vascular functionality. We highlight three core mechanistic dimensions: bidirectionality, temporal dynamics, and tissue specificity, and further emphasize the functional synergy emerging from their network-level interactions. Building on these features, we propose the functional vascular normalization score (FVNS) and the chemokine-guided vascular normalization window (VNW) as molecular tools for real-time vascular assessment and therapeutic stratification. Finally, we outline CXC-targeted strategies, including CXCR2/CXCR4 blockade, CXCL9/10/11 augmentation, and spatiotemporally controlled delivery platforms, which may extend and personalize the VNW. This chemokine-focused paradigm provides a functional and implementable approach for the integration of vascular normalization and immune modulation in cancer therapy.
Authors
- Ziying Yi (ORCID: https://orcid.org/0000-0002-5462-5212)
- Chong Li (ORCID: https://orcid.org/0000-0001-6375-0181)
- Yao Li (ORCID: https://orcid.org/0009-0007-2980-5274)
- Wu
- Yinde Huang
- Fan Zhang
- Hongdan Chen
- Zeyu Yang
Institutions
- Southwest University (CN)
- First People's Hospital of Chongqing (CN)
- Chongqing Medical and Pharmaceutical College (CN)
- Southern Medical University (CN)
Publication Details
- Journal
- Advanced Science
- Published
- 2026-01-20
- DOI
- https://doi.org/10.1002/advs.202523331
- Primary Topic
- Angiogenesis and VEGF in Cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00