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        <identifier>oai:figshare.com:article/34023546</identifier>
        <datestamp>2026-09-29T11:57:34Z</datestamp>
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          <dc:title>Image_1_A Penicillin Derivative Exerts an Anti-Metastatic Activity in Melanoma Cells Through the Downregulation of Integrin αvβ3 and Wnt/β-Catenin Pathway.tif</dc:title>
          <dc:creator>Elizabeth Barrionuevo (8488278)</dc:creator>
          <dc:creator>Florencia Cayrol (8488281)</dc:creator>
          <dc:creator>Graciela A. Cremaschi (8488284)</dc:creator>
          <dc:creator>Patricia G. Cornier (5798657)</dc:creator>
          <dc:creator>Dora B. Boggián (8488287)</dc:creator>
          <dc:creator>Carina M. L. Delpiccolo (8488290)</dc:creator>
          <dc:creator>Ernesto G. Mata (1581094)</dc:creator>
          <dc:creator>Leonor P. Roguin (8488293)</dc:creator>
          <dc:creator>Viviana C. Blank (8488296)</dc:creator>
          <dc:subject>Basic Pharmacology</dc:subject>
          <dc:subject>Clinical Pharmacology and Therapeutics</dc:subject>
          <dc:subject>Clinical Pharmacy and Pharmacy Practice</dc:subject>
          <dc:subject>Pharmaceutical Sciences</dc:subject>
          <dc:subject>Pharmacogenomics</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Toxicology (incl. Clinical Toxicology)</dc:subject>
          <dc:subject>Pharmacology and Pharmaceutical Sciences not elsewhere classified</dc:subject>
          <dc:subject>triazolylpeptidyl penicillin</dc:subject>
          <dc:subject>anti-metastatic effect</dc:subject>
          <dc:subject>murine melanoma</dc:subject>
          <dc:subject>β-catenin</dc:subject>
          <dc:subject>metalloproteinases-2 and -9</dc:subject>
          <dc:subject>integrin αvβ3</dc:subject>
          <dc:description>&lt;p&gt;The synthetic triazolylpeptidyl penicillin derivative, named TAP7f, has been previously characterized as an effective antitumor agent in vitro and in vivo against B16-F0 melanoma cells. In this study, we investigated the anti-metastatic potential of this compound on highly metastatic murine B16-F10 and human A375 melanoma cells. We found that TAP7f inhibited cell adhesion, migration and invasion in a dose-dependent manner. Additionally, we demonstrated that TAP7f downregulated integrin αvβ3 expression and Wnt/β-catenin pathway, a signaling cascade commonly related to tumor invasion and metastasis. Thus, TAP7f reduced both the enzymatic activity and the expression levels of matrix-metalloproteinases-2 and -9 in a time dependent manner. Moreover, TAP7f inhibited the expression of the transcription factor Snail and the mesenchymal markers vimentin, and N-cadherin, and up-regulated the expression of the epithelial marker E-cadherin, suggesting that the penicillin derivative affects epithelial–mesenchymal transition. Results obtained in vitro were supported by those obtained in a B16-F10-bearing mice metastatic model, that showed a significant TAP7f inhibition of lung metastasis. These findings suggest the potential of TAP7f as a chemotherapeutic agent for the treatment of metastatic melanoma.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-29T11:57:34Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.3389/fphar.2020.00127.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/figure/Image_1_A_Penicillin_Derivative_Exerts_an_Anti-Metastatic_Activity_in_Melanoma_Cells_Through_the_Downregulation_of_Integrin_v_3_and_Wnt_-Catenin_Pathway_tif/34023546</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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