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2000
Volume 24, Issue 17
  • ISSN: 1389-4501
  • E-ISSN: 1873-5592

Abstract

Pancreatic cancer (PC) is one the most lethal malignancies worldwide affecting around half a million individuals each year. The treatment of PC is relatively difficult due to the difficulty in making an early diagnosis. Transforming growth factor-beta (TGF-β) is a multifunctional factor acting as both a tumor promoter in early cancer stages and a tumor suppressor in advanced disease. Programmed death-ligand 1 (PD-L1) is a ligand of programmed death-1 (PD-1), an immune checkpoint receptor, allowing tumor cells to avoid elimination by immune cells. Recently, targeting the TGF-β signaling and PD-L1 pathways has emerged as a strategy for cancer therapy. In this review, we have summarized the current knowledge regarding these pathways and their contribution to tumor development with a focus on PC. Moreover, we have reviewed the role of TGF-β and PD-L1 blockade in the treatment of various cancer types, including PC, and discussed the clinical trials evaluating TGF-β and PD-L1 antagonists in PC patients.

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/content/journals/cdt/10.2174/0113894501264450231129042256
2023-12-01
2025-05-22
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/content/journals/cdt/10.2174/0113894501264450231129042256
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  • Article Type:
    Review Article
Keyword(s): cancer patients; carcinogenesis; cytotoxic T cells; Pancreatic cancer; PD-L1; TGF-β
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