Petra Gener

Dr. Petra Gener


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2015 in Nanomedicine: Nanotechnology, Biology and Medicine
Verified
Journal Article
Closed access
PGPetra Gener
Petra Gener
Luis Pleno GouveiaLuis Pleno Gouveia
Luis Pleno Gouveia
GSGuillem Romero Sabat
Guillem Romero Sabat
Diana RafaelDiana Rafael
Diana Rafael
NFNúria Bergadà Fort
Núria Bergadà Fort
Simó Schwartz Jr.Simó Schwartz Jr.
Simó Schwartz Jr.

1 January 2021 in Cancer Drug Resistance
Verified
Journal Article
Open access
PDF file
AUAnna Ulldemolins
Anna Ulldemolins
JSJoaquin Seras-Franzoso
Joaquin Seras-Franzoso
FAFernanda Andrade
Fernanda Andrade
DRDiana Rafael
Diana Rafael
IAIbane Abasolo
Ibane Abasolo
Simó Schwartz Jr.Simó Schwartz Jr.
Simó Schwartz Jr.
Cancer Drug Resistance is an open access journal, focusing on pharmacological aspects of drug resistance and its reversal, molecular mechanisms of drug resistance and drug classes, etc. Both clinical and experimental aspects of drug resistance in cancer are included.

1 February 2020 in Nanomedicine: Nanotechnology, Biology and Medicine
Verified
Journal Article
Open access
PGPetra Gener
Petra Gener
SMSara Montero
Sara Montero
HXHelena Xandri-Monje
Helena Xandri-Monje
ZDZamira V. Díaz-Riascos
Zamira V. Díaz-Riascos
DRDiana Rafael
Diana Rafael
Simó Schwartz Jr.Simó Schwartz Jr.
Simó Schwartz Jr.
Tumor recurrence, metastatic spread and progressive gain of chemo-resistance of advanced cancers are sustained by the presence of cancer stem cells (CSCs) within the tumor. Targeted therapies with the aim to eradicate these cells are thus highly regarded. However, often the use of new anti-cancer therapies is hampered by pharmacokinetic demands. Drug delivery through nanoparticles has great potential to increase efficacy and reduce toxicity and adverse effects. However, its production has to be based on intelligent design. Likewise, we developed polymeric nanoparticles loaded with Zileuton™, a potent inhibitor of cancer stem cells (CSCs), which was chosen based on high throughput screening. Its great potential for CSCs treatment was subsequently demonstrated in in vitro and in in vivo CSC fluorescent models. Encapsulated Zileuton™ reduces amount of CSCs within the tumor and effectively blocks the circulating tumor cells (CTCs) in the blood stream and metastatic spread.

1 October 2015 in Nanomedicine: Nanotechnology, Biology and Medicine
Verified
Journal Article
Closed access
FAFernanda da Silva Andrade
Fernanda da Silva Andrade
José das NevesJosé das Neves
José das Neves
PGPetra Gener
Petra Gener
Simó Schwartz Jr.Simó Schwartz Jr.
Simó Schwartz Jr.
DFDomingos Ferreira
Domingos Ferreira
Bruno SarmentoBruno Sarmento
Bruno Sarmento

1 January 2018 in Drug Delivery
Verified
Journal Article
Open access
Diana RafaelDiana Rafael
Diana Rafael
PGPetra Gener
Petra Gener
FAFernanda da Silva Andrade
Fernanda da Silva Andrade
JSJoaquin Seras-Franzoso
Joaquin Seras-Franzoso
SMSara Montero
Sara Montero
MVMafalda Videira
Mafalda Videira
Development of RNA interference-based therapies with appropriate therapeutic window remains a challenge for advanced cancers. Because cancer stem cells (CSC) are responsible of sustaining the metastatic spread of the disease to distal organs and the progressive gain of resistance of advanced cancers, new anticancer therapies should be validated specifically for this subpopulation of cells. A new amphihilic-based gene delivery system that combines Pluronic® F127 micelles with polyplexes spontaneously formed by electrostatic interaction between anionic siRNA and cationic polyethylenimine (PEI) 10K, was designed (PM). Resultant PM gather the requirements for an efficient and safe transport of siRNA in terms of its physicochemical characteristics, internalization capacity, toxicity profile and silencing efficacy. PM were loaded with a siRNA against AKT2, an important oncogene involved in breast cancer tumorigenesis, with a special role in CSC malignancy. Efficacy of siAKT2-PM was validated in CSC isolated from two breast cancer cell lines: MCF-7 and Triple Negative MDA-MB-231 corresponding to an aggressive subtype of breast cancer. In both cases, we observed significant reduction on cell invasion capacity and strong inhibition of mammosphere formation after treatment. These results prompt AKT2 inhibition as a powerful therapeutic target against CSC and pave the way to the appearance of more effective nanomedicine-based gene therapies aimed to prevent CSC-related tumor recurrence.

26 November 2020 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
LHLaia Hernandez-Oller
Laia Hernandez-Oller
JSJoaquin Seras-Franzoso
Joaquin Seras-Franzoso
FAFernanda da Silva Andrade
Fernanda da Silva Andrade
Diana RafaelDiana Rafael
Diana Rafael
IAIbane Abasolo
Ibane Abasolo
Simó Schwartz Jr.Simó Schwartz Jr.
Simó Schwartz Jr.
Within tumors, Cancer Stem Cell (CSC) subpopulation has an important role in maintaining growth and dissemination while preserving high resistance against current treatments. It has been shown that, when CSCs are eliminated, the surrounding Differentiated Cancer Cells (DCCs) may reverse their phenotype and gain CSC-like features to preserve tumor progression and ensure tumor survival. This strongly suggests the existence of paracrine communication within tumor cells. It is evidenced that the molecular crosstalk is at least partly mediated by Extracellular Vesicles (EVs), which are cell-derived membranous nanoparticles that contain and transport complex molecules that can affect and modify the biological behavior of distal cells and their molecular background. This ability of directional transport of small molecules prospects EVs as natural Drug Delivery Systems (DDS). EVs present inherent homing abilities and are less immunogenic than synthetic nanoparticles, in general. Currently, strong efforts are focused into the development and improvement of EV-based DDS. Even though EV-DDS have already reached early phases in clinical trials, their clinical application is still far from commercialization since protocols for EVs loading, modification and isolation need to be standardized for large-scale production. Here, we summarized recent knowledge regarding the use of EVs as natural DDS against CSCs and cancer resistance.