Role of the Extracellular Matrix in Cancer: Insights into Tumor Progression and Therapy

被引:7
作者
Desai, Nimeet [1 ]
Sahel, Deepak [2 ]
Kubal, Bhakti [3 ]
Postwala, Humzah [4 ]
Shah, Yesha [4 ]
Chavda, Vivek P. [5 ]
Fernandes, Clara [3 ]
Khatri, Dharmendra K. [6 ]
Vora, Lalitkumar K. [7 ]
机构
[1] Univ Liverpool, Dept Eye & Vis Sci, Liverpool L7 8TX, England
[2] Oregon State Univ, Coll Pharm, Dept Pharmaceut Sci, Portland, OR 97201 USA
[3] Bombay Coll Pharm, Dept Pharmaceut, Kalina 400098, Mumbai, India
[4] LM Coll Pharm, Dept Pharmacol & Pharm Practice, Ahmadabad 380009, India
[5] LM Coll Pharm, Dept Pharmaceut & Pharmaceut Technol, Ahmadabad 380009, India
[6] NIMS Univ Rajasthan, NIMS Inst Pharm, Dept Pharmacol, Jaipur 303121, India
[7] Queens Univ Belfast, Sch Pharm, 97 Lisburn Rd, Belfast BT9 7BL, North Ireland
关键词
cancer; collagen-targeted therapy; extracellular matrix; hyaluronan inhibition; matrix stiffness regulation; NOTCH SIGNALING PATHWAY; HEPATIC STELLATE CELLS; TGF-BETA; LYSYL OXIDASE; GROWTH-FACTOR; REPLICATIVE SENESCENCE; PREMATURE SENESCENCE; DERMAL FIBROBLASTS; GENE-EXPRESSION; HYALURONIC-ACID;
D O I
10.1002/adtp.202400370
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The extracellular matrix (ECM) serves not only as a structural scaffold but also as an active regulator of cancer progression, profoundly influencing tumor behaviour and the tumor microenvironment (TME). This review focuses into the pivotal role of ECM alterations in facilitating tumor metastasis and explores therapeutic strategies aimed at counteracting these changes. We analyse targeted interventions against collagen, including approaches to inhibit its biosynthesis and disrupt associated signalling pathways critical for tumor architecture and cell migration. Additionally, therapies addressing hyaluronan are reviewed, highlighting methods to suppress its synthesis and enzymatic strategies to degrade it, thereby mitigating its tumor-promoting effects. The discussion extends to innovative approaches for modulating ECM stiffness, focusing on the roles of cancer-associated fibroblasts and lysyl oxidases, which are key contributors to ECM remodelling and mechanical signalling. By strategically modifying these ECM components, these interventions aim to enhance the efficacy of existing cancer treatments, tackle resistance mechanisms, and achieve more durable therapeutic outcomes. Insights from recent studies and clinical trials highlight the promise of these strategies in overcoming treatment resistance and improving patient outcomes. Advancing our understanding of ECM biology leads to the development of innovative and more effective cancer therapies.
引用
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页数:41
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