Development of anti-membrane type 1-matrix metalloproteinase nanobodies as immunoPET probes for triple negative breast cancer imaging.
| dc.contributor.author | Mulero, Francisca | |
| dc.contributor.author | Oteo, Marta | |
| dc.contributor.author | Garaulet, Guillermo | |
| dc.contributor.author | Magro, Natalia | |
| dc.contributor.author | Rebollo, Lluvia | |
| dc.contributor.author | Medrano, Guillermo | |
| dc.contributor.author | Santiveri, Clara | |
| dc.contributor.author | Romero, Eduardo | |
| dc.contributor.author | Sellek, Ricela E. | |
| dc.contributor.author | Margolles, Yago | |
| dc.contributor.author | Campos-Olivas, Ramón | |
| dc.contributor.author | Arroyo, Alicia | |
| dc.contributor.author | Fernández, Luis Ángel | |
| dc.contributor.author | Morcillo, Miguel Ángel | |
| dc.contributor.author | Martínez-Torrecuadrada, Jorge L. | |
| dc.date.accessioned | 2024-02-01T10:30:20Z | |
| dc.date.available | 2024-02-01T10:30:20Z | |
| dc.date.issued | 2024-02-01 | |
| dc.description.abstract | Triple-negative breast cancer (TNBC) is characterized by aggressiveness and high rates of metastasis. The identification of relevant biomarkers is crucial to improve outcomes for TNBC patients. Membrane type 1-matrix metalloproteinase (MT1-MMP) could be a good candidate because its expression has been reported to correlate with tumor malignancy, progression and metastasis. Moreover, single-domain variable regions (VHHs or Nanobodies) derived from camelid heavy-chain-only antibodies have demonstrated improvements in tissue penetration and blood clearance, important characteristics for cancer imaging. Here, we have developed a nanobody-based PET imaging strategy for TNBC detection that targets MT1-MMP. A llama-derived library was screened against the catalytic domain of MT1-MMP and a panel of specific nanobodies were identified. After a deep characterization, two nanobodies were selected to be labeled with gallium-68 (68Ga). ImmunoPET imaging with both ([68Ga]Ga-NOTA-3TPA14 and [68Ga]Ga-NOTA-3CMP75) in a TNBC mouse model showed precise tumor-targeting capacity in vivo with high signal-to-background ratios. (68Ga)Ga-NOTA-3CMP75 exhibited higher tumor uptake compared to (68Ga)Ga-NOTA-3TPA14. Furthermore, imaging data correlated perfectly with the immunohistochemistry staining results. In conclusion, we found a promising candidate for nanobody-based PET imaging to be further investigated as a diagnostic tool in TNBC. | es_ES |
| dc.identifier.doi | http://dx.doi.org/10.3389/fmed.2022.1058455 | |
| dc.identifier.other | eISSN: 2296-858X | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14855/2294 | |
| dc.language.iso | eng | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.subject | MT1-MMP | es_ES |
| dc.subject | TNBC (triple negative breast cancer) | es_ES |
| dc.subject | gallium-68 | es_ES |
| dc.subject | immunoPET | es_ES |
| dc.subject | nanobodies | es_ES |
| dc.title | Development of anti-membrane type 1-matrix metalloproteinase nanobodies as immunoPET probes for triple negative breast cancer imaging. | es_ES |
| dc.type | journal article | es_ES |
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