Abstract | OBJECTIVE: METHODS: Immunoexpression of PAI-1 was analyzed in 60 OTSCC specimens and classified as low-expression (≤50% of positive cells) or high-expression (>50%). In vitro effects of recombinant human PAI-1 (rhPAI-1) were assessed through functional assays on the OTSCC-derived cell line SCC-25. Three cell groups were evaluated: G0 (control), G10 (10 nM rhPAI-1), and G20 (20 nM rhPAI-1). RESULTS: High membrane expression of PAI-1 was associated with tumor budding (p = 0.046) and high-risk cases (p = 0.043). Cytoplasmic and membrane expression of PAI-1 was not associated with patient survival. Cell viability (p = 0.020) and progression to the S-phase of the cell cycle (p = 0.024) were higher in G10 and G20 at 24 h. The percentages of apoptotic/necrotic cells were not affected by rhPAI-1. The presence of rhPAI-1 increased cell migration (p = 0.039) and invasion (p = 0.039) after 24 and 72 h, respectively. CONCLUSION: Our findings indicate the involvement of PAI-1 in the biological behavior of OTSCC, although its expression may not predict patient survival. The in vitro results suggest that PAI-1 stimulates cell proliferation, migration and invasion and may contribute to the aggressive phenotype of OTSCC.
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Authors | Rodrigo Porpino Mafra, Vladimir Galdino Sabino, Larissa Santos Amaral Rolim, Cyntia Helena Pereira de Carvalho, Cassiano Francisco Weege Nonaka, Carlos Augusto Galvão Barboza, Lélia Batista de Souza, Leão Pereira Pinto |
Journal | Experimental and molecular pathology
(Exp Mol Pathol)
Vol. 124
Pg. 104722
(02 2022)
ISSN: 1096-0945 [Electronic] Netherlands |
PMID | 34800515
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2021 Elsevier Inc. All rights reserved. |
Chemical References |
- Plasminogen Activator Inhibitor 1
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Carcinoma, Squamous Cell
(metabolism, pathology)
- Cell Line, Tumor
- Female
- Humans
- Immunohistochemistry
- Male
- Middle Aged
- Plasminogen Activator Inhibitor 1
(metabolism)
- Prognosis
- Retrospective Studies
- Squamous Cell Carcinoma of Head and Neck
(metabolism, pathology)
- Tongue Neoplasms
(metabolism, pathology)
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