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Daiane Rosolen

Bio: Daiane Rosolen is an academic researcher from Universidade Federal de Santa Catarina. The author has contributed to research in topics: microRNA & Apoptosis. The author has an hindex of 3, co-authored 5 publications receiving 26 citations.

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TL;DR: The results showed twenty altered miRNAs between no ACLF and ACLF patients, and twenty-seven in patients who died in 30 days compared with who survived, and of these, miR-25-3p was independently related to ACLf and 30-day mortality.
Abstract: Acute-on-chronic liver failure (ACLF) is a condition characterized by acute decompensation of cirrhosis, associated with organ failure(s), and high short-term mortality. The microRNAs or miRNAs are small non-coding RNA molecules, stable in circulating samples such as biological fluids, and the difference in expression levels may indicate the presence, absence and/or stage of the disease. We analyzed here the miRNA profiling to identify potential diagnostic or prognostic biomarkers for ACLF. The major miRNAs discovered were validated in a cohort of patients with acute decompensation of cirrhosis grouped in no ACLF or ACLF according to EASL-CLIF definition. Relationship between serum miRNAs and variables associated with liver-damage and survival outcomes were verified to identify possible prognostic markers. Our results showed twenty altered miRNAs between no ACLF and ACLF patients, and twenty-seven in patients who died in 30 days compared with who survived. In validation phase, miR-223-3p and miR-25-3p were significantly altered in ACLF patients and in those who died in 30 days. miR-223-3p and miR-25-3p expression were associated with the lowest survival in 30 days. The decrease in miR-223-3p and miR-25-3p expression was associated with the presence of ACLF and poor prognosis. Of these, miR-25-3p was independently related to ACLF and 30-day mortality.

18 citations

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TL;DR: In this paper, the expression profile of exosomal microRNAs (miRNAs) derived from metastatic prostate cancer (mPCa) cell lines (LNCaP and PC-3) was evaluated by miRNA microarray analysis.

13 citations

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TL;DR: M1 and M5 presented antiadipogenic and antitumoral activities that was associated to apoptosis and necrosis is a possible consequence of the FASN reduction, which in turn might result in a fuel decrease to cell proliferation.

10 citations

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TL;DR: It was strongly confirmed that maleimide derivatives promoted cell death in leukemia cells triggered by oxidative stress, indicating that these compounds might be promising antitumor agents or lead molecules.
Abstract: Maleimides consist of an important class of compounds easily synthesized with multiple functional group modification that provides expressive pharmacological properties including, antitumoral activity, mediated mainly by oxidative stress. For this reason, the present study was designed to evaluate the cytotoxicity and the role of reactive oxygen species (ROS) in maleimide-induced cell death. Cell viability assays were performed to determine the cell death type in leukemia cell line induced by the compounds. The oxidative stress in maleimidetreated cells was characterized by antioxidant enzymes activities, intracellular ROS generation, and lipid peroxidation. In addition, we evaluated mitochondrial membrane potential and ATP level. Maleimide derivatives exhibited cytotoxic effects in leukemia cells with significantly increased ROS generation. However, cell viability was partly restored by catalase-treated cells. Caspases activities and caspase-independent key genes related to apoptosis were not altered by maleimides, suggesting necrosis as the main cell death process. Maleimide-induced necrosis was associated with oxidative stress, as an imbalance between ROS levels and glutathione reductase (GR) activity. This damage was also demonstrated by loss of mitochondrial membrane potential (MMP) and ATP depletion in cells treated with maleimide derivatives. These findings strongly confirmed that maleimide derivatives promoted cell death in leukemia cells triggered by oxidative stress, indicating that these compounds might be promising antitumor agents or lead molecules.

5 citations

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TL;DR: In this article , the authors determined the chemical composition and evaluated the antioxidant activity and antifungal properties of essential oils of oregano and mint against the fungi Aspergillus flavus and Penicillium commune as possible alternatives for food preservation.
Abstract: This study determined the chemical composition and evaluated the antioxidant activity and antifungal properties of essential oils of oregano (Origanum vulgare) and mint (Mentha arvensis) against the fungi Aspergillus flavus and Penicillium commune as possible alternatives for food preservation. The antimicrobial activity of both oils is shown by their minimum inhibitory concentration (4 mg/mL) for oregano oil, and (8 mg/mL) for mint oil, and minimum inhibitory dose (< 110 µl/L) for oregano oil, and (< 1500 µL/L) for mint oil. In addition, both oils presented antioxidant activity superior to 70% at the concentrations of 0.5 mg/mL for oregano oil and 30 mg/mL for mint oil after 360 min of reaction. As a control, the oils were evaluated for their cytotoxic potential using cells in culture and the method based on mitochondrial activity. Both oils were cytotoxic to both cell lines tested, with cells' survival rates less than 20% when in contact with 25 μg/mL of oils concentrations. Overall, the essential oils have activity against Aspergillus flavus and Penicillium commune, and their volatile components expressed high antifungal activity that expands their use for situations in which direct contact with the liquid is undesired. However, both essential oils showed high cytotoxicity.

3 citations


Cited by
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TL;DR: How the tumor and its microenvironment influences T cell trafficking and function with a focus on melanoma, and pancreatic and ovarian cancer, is discussed, and how scientific advances may help overcome these hurdles are discussed.

453 citations

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TL;DR: The attention will be focused on the contribution of ROS to the signaling of HIF, NFκB, and Sirtuins as a leitmotif of cancer initiation and progression.
Abstract: The presence of ROS is a constant feature in living cells metabolizing O2. ROS concentration and compartmentation determine their physiological or pathological effects. ROS overproduction is a feature of cancer cells and plays several roles during the natural history of malignant tumor. ROS continuously contribute to each step of cancerogenesis, from the initiation to the malignant progression, acting directly or indirectly. In this review, we will (a) underline the role of ROS in the pathway leading a normal cell to tumor transformation and progression, (b) define the multiple roles of ROS during the natural history of a tumor, (c) conciliate many conflicting data about harmful or beneficial effects of ROS, (d) rethink the importance of oncogene and tumor suppressor gene mutations in relation to the malignant progression, and (e) collocate all the cancer hallmarks in a mechanistic sequence which could represent a "physiological" response to the initial growth of a transformed stem/pluripotent cell, defining also the role of ROS in each hallmark. We will provide a simplified sketch about the relationships between ROS and cancer. The attention will be focused on the contribution of ROS to the signaling of HIF, NFκB, and Sirtuins as a leitmotif of cancer initiation and progression.

239 citations

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TL;DR: HFD‐fed miR‐223KO mice develop a full spectrum ofNAFLD, representing a clinically relevant mouse NAFLD model; miR •223 plays a key role in controlling steatosis‐to‐NASH progression by inhibiting hepatic Cxcl10 and Taz expression and may be a therapeutic target for the treatment of NASH.

87 citations

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TL;DR: In this paper, the specific miRNA profile which can act as new biomarkers for distinguishing acute respiratory syndrome coronavirus 2 (COVID-19) from the healthy group and those in the post-acute phase of the disease was elucidated.

59 citations

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TL;DR: In this paper , a review of exosomal miRNAs (liquid biopsy) as biomarkers in the diagnosis and prognosis of various cancers is presented. But the authors focus on the use of liquid biopsies as a supplement to biopsy, as it enables disease progression to be detected months before clinical and radiographic confirmation.
Abstract: Detecting cancer at an early stage before clinical manifestation could be an effective strategy to decrease cancer mortality. Thus, identifying liquid biopsy biomarkers with high efficacy could be a promising approach for non-invasive diagnosis of cancer.Liquid biopsies are increasingly used as a supplement to biopsy, as it enables disease progression to be detected months before clinical and radiographic confirmation. Many bodily fluids contain exosomal microRNAs (miRNAs) which could provide a new class of biomarkers for early and minimally invasive cancer diagnosis due to the stability of miRNAs in exosomes. In this review, we mainly focused on the exosomal miRNAs (liquid biopsy) as biomarkers in the diagnosis and prognosis of various cancers.Exosomal miRNAs can be used as diagnostic and prognosis biomarkers that provide unique insights and a more dynamic perspective of the progression and therapeutic responses in various malignancies. Therefore, the development of novel and more sensitive technologies that exploit exosomal miRNAs should be a priority for cancer management.

45 citations