Publications

Sort by: Author [ Title  (Asc)] Type Year
A B C D E F G H I J K L M N O P Q R S [T] U V W X Y Z   [Show ALL]
T
Alves-Barroco, C., L. Rivas-García, A. R. Fernandes, and P. V. Baptista. "Tackling Multidrug Resistance in Streptococci - From Novel Biotherapeutic Strategies to Nanomedicines." Front Microbiol 11 (2020): 579916. AbstractWebsite

n/a

Pedrosa, Pedro, Luísa M. Corvo, Margarida Ferreira-Silva, Pedro Martins, Manuela Colla Carvalheiro, Pedro M. Costa, Carla Martins, L. M. D. R. S. Martins, Pedro V. Baptista, and Alexandra R. Fernandes. "Targeting Cancer Resistance via Multifunctional Gold Nanoparticles." International Journal of Molecular Sciences 20 (2019). AbstractWebsite

Resistance to chemotherapy is a major problem facing current cancer therapy, which is continuously aiming at the development of new compounds that are capable of tackling tumors that developed resistance toward common chemotherapeutic agents, such as doxorubicin (DOX). Alongside the development of new generations of compounds, nanotechnology-based delivery strategies can significantly improve the in vivo drug stability and target specificity for overcoming drug resistance. In this study, multifunctional gold nanoparticles (AuNP) have been used as a nanoplatform for the targeted delivery of an original anticancer agent, a Zn(II) coordination compound [Zn(DION)2]Cl2 (ZnD), toward better efficacy against DOX-resistant colorectal carcinoma cells (HCT116 DR). Selective delivery of the ZnD nanosystem to cancer cells was achieved by active targeting via cetuximab, NanoZnD, which significantly inhibited cell proliferation and triggered the death of resistant tumor cells, thus improving efficacy. In vivo studies in a colorectal DOX-resistant model corroborated the capability of NanoZnD for the selective targeting of cancer cells, leading to a reduction of tumor growth without systemic toxicity. This approach highlights the potential of gold nanoformulations for the targeting of drug-resistant cancer cells.

Pedrosa, P., M. L. Corvo, M. Ferreira-Silva, P. Martins, MC Carvalheiro, P. M. Costa, C. Martins, D.RS L. M. Martins, P. V. Baptista, and A. R. Fernandes. "Targeting Cancer Resistance via Multifunctional Gold Nanoparticles." Int J Mol Sci 20 (2019). AbstractWebsite

n/a

Raposo, L. R., C. Roma-Rodrigues, J. Jesus, L. M. D. R. S. Martins, A. J. Pombeiro, P. V. Baptista, and A. R. Fernandes. "Targeting canine mammary tumours via gold nanoparticles functionalized with promising Co(II) and Zn(II) compounds." Veterinary and Comparative Oncology 15 (2017): 1537-1542. Abstract

n/a

Roma-Rodrigues, C., R. Mendes, P. V. Baptista, and A. R. Fernandes. "Targeting Tumor Microenvironment for Cancer Therapy." Int J Mol Sci 20 (2019). AbstractWebsite

n/a

Roma-Rodrigues, Catarina, Luis Raposo, Rita Cabral, Fabiana Paradinha, Pedro V. Baptista, and Alexandra R. Fernandes. "Tumor microenvironment modulation via gold nanoparticles targeting malicious exosomes: implications in cancer diagnostics and Therapy." Int. J. Mol. Sci. 18 (2017): 162. AbstractWebsite

Exosomes are nanovesicles formed in the endosomal pathway with an important role in paracrine and autocrine cell communication. Exosomes secreted by cancer cells, malicious exosomes, have important roles in tumor microenvironment maturation and cancer progression. The knowledge of the role of exosomes in tumorigenesis prompted a new era in cancer diagnostics and therapy, taking advantage of the use of circulating exosomes as tumor biomarkers due to their stability in body fluids and targeting malignant exosomes’ release and/or uptake to inhibit or delay tumor development. In recent years, nanotechnology has paved the way for the development of a plethora of new diagnostic and therapeutic platforms, fostering theranostics. The unique physical and chemical properties of gold nanoparticles (AuNPs) make them suitable vehicles to pursuit this goal. AuNPs’ properties such as ease of synthesis with the desired shape and size, high surface:volume ratio, and the possibility of engineering their surface as desired, potentiate AuNPs’ role in nanotheranostics, allowing the use of the same formulation for exosome detection and restraining the effect of malicious exosomes in cancer progression.