Plasminogen activator inhibitor-1 as an oncologic target: biology, therapeutic inhibitors, and clinical translation

Plasminogen activator inhibitor-1 (PAI-1) is a key regulator of cancer biology, influencing tumor progression, metastasis, and therapeutic resistance. Elevated levels of PAI-1 are consistently associated with poor prognosis across several malignancies, including breast, ovarian, lung, hepatobiliary, colorectal, and glioblastoma. Mechanistically, PAI-1 facilitates cancer cell survival, endothelial migration, and immune modulation. From a therapeutic standpoint, PAI-1 represents a promising target. Strategies to inhibit PAI-1, including small-molecule inhibitors and monoclonal antibodies, have demonstrated promise in preclinical research. Collectively, these findings underscore both the therapeutic potential and the translational challenges associated with targeting PAI-1 in future cancer treatment. This review examines the mechanistic foundations of the PAI-1 paradox, its prognostic and therapeutic implications in cancer, and the opportunities and challenges for clinical translation.

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Publication Details

Journal
Frontiers in Oncology
Published
2026-04-01
DOI
https://doi.org/10.3389/fonc.2026.1737975
Primary Topic
Protease and Inhibitor Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

Plasminogen activator inhibitor-1 as an oncologic target: biology, therapeutic inhibitors, and clinical translation

Ahmed Yaqinuddin, Nada Saed Homod Al Shaer, Mohammed Imran Khan, Maryam Alawi Al-Attas et al.
Frontiers in Oncology
Protease and Inhibitor Mechanisms
article

Plasminogen activator inhibitor-1 as an oncologic target: biology, therapeutic inhibitors, and clinical translation

Ahmed Yaqinuddin, Nada Saed Homod Al Shaer, Mohammed Imran Khan, Maryam Alawi Al-Attas, Aya Tleyjeh, Joudi Haitham Alibrahim
article en

Abstract

Plasminogen activator inhibitor-1 (PAI-1) is a key regulator of cancer biology, influencing tumor progression, metastasis, and therapeutic resistance. Elevated levels of PAI-1 are consistently associated with poor prognosis across several malignancies, including breast, ovarian, lung, hepatobiliary, colorectal, and glioblastoma. Mechanistically, PAI-1 facilitates cancer cell survival, endothelial migration, and immune modulation. From a therapeutic standpoint, PAI-1 represents a promising target. Strategies to inhibit PAI-1, including small-molecule inhibitors and monoclonal antibodies, have demonstrated promise in preclinical research. Collectively, these findings underscore both the therapeutic potential and the translational challenges associated with targeting PAI-1 in future cancer treatment. This review examines the mechanistic foundations of the PAI-1 paradox, its prognostic and therapeutic implications in cancer, and the opportunities and challenges for clinical translation.

Frontiers in OncologyVol. 16
Alfaisal University (SA), King Faisal Specialist Hospital & Research Centre (SA)
No poverty
Openalex Percentile: Top 35%
Protease and Inhibitor Mechanisms
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