Publications by authors named "Ana M Chudzinski-Tavassi"

Article Synopsis
  • Melanoma is a aggressive skin cancer that is hard to treat due to its ability to spread, making targeted therapies and immunotherapies necessary but challenging.
  • Crotoxin (CTX), a toxin from snake venom, shows promise for anti-cancer effects, especially against melanoma, though its high toxicity limits its use in clinical settings.
  • This study found that both native and detoxified CTX were effective at killing melanoma cells, triggering cell death and preventing their proliferation, with the detoxified version showing less harmful effects, paving the way for safer CTX-based treatments.
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  • It emphasizes [another important aspect or argument] and presents evidence or examples such as [specific detail or study].
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Snake bites are a severe problem in the countryside of Brazil and are usually attributed to snakes of the genera Bothrops, Crotalus, and Lachesis. Snake venom can release ectoenzymes and nucleotidases that modulate the purinergic system. In addition to serum therapy against snake poisoning, medicinal plants with anti-inflammatory activities, such as Tabebuia aurea, is empirically applied in accidents that occur in difficult-to-access areas.

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Most anti-inflammatory drugs currently adopted to treat chronic inflammatory joint diseases can alleviate symptoms but they do not lead to remission. Therefore, new and more efficient drugs are needed to block the course of joint inflammatory diseases. Animal venoms, rich in bioactive compounds, can contribute as valuable tools in this field of research.

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Transplanted mesenchymal stromal cells (MSCs) exhibit a robust anti-inflammatory and homing capacity in response to high inflammatory signals, as observed in studies focused on rheumatic diseases that target articular cartilage (AC) health. However, AC degradation in osteoarthritis (OA) does not necessarily coincide with a highly inflammatory joint profile. Often, by the time patients seek medical attention, they already have damaged AC.

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Introduction: Osteolytic bone metastasis in advanced breast cancer stages are a major complication for patient´s quality life and a sign of low survival prognosis. Permissive microenvironments which allow cancer cell secondary homing and later proliferation are fundamental for metastatic processes. The causes and mechanisms behind bone metastasis in breast cancer patients are still an unsolved puzzle.

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been responsible for the severe pandemic of acute respiratory disease, coronavirus disease 2019 (COVID-19), experienced in the 21st century. The clinical manifestations range from mild symptoms to abnormal blood coagulation and severe respiratory failure. In severe cases, COVID-19 manifests as a thromboinflammatory disease.

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Salivary glands are vital structures responsible for successful tick feeding. The saliva of ticks contains numerous active molecules that participate in several physiological processes. A Kunitz-type factor Xa (FXa) inhibitor, similar to the tissue factor pathway inhibitor (TFPI) precursor, was identified in the salivary gland transcriptome of ticks.

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The COVID-19 pandemic caused by the severe acute syndrome virus 2 (SARS-CoV-2) has been around since November 2019. As of early June 2022, more than 527 million cases were diagnosed, with more than 6.0 million deaths due to this disease.

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The pursuit of better therapies for disorders creating deficiencies in skeletal muscle regeneration is in progress, and several biotoxins are used in skeletal muscle research. Since recombinant proteins derived from Lonomia obliqua bristles, recombinant Lonomia obliqua Stuart-factor activator (rLosac) and recombinant Lonomia obliqua prothrombin activator protease (rLopap) act as cytoprotective agents and promote cell survival, we hypothesize that both rLosac and rLopap favour the skeletal muscle regeneration process. In the present work, we investigate the ability of these recombinant proteins rLosac and rLopap to modulate the production of key mediators of the myogenic process.

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The COVID-19 pandemic, caused by SARS-CoV-2, had its first cases identified in late 2019 and was considered a clinical pandemic in March 2020. In March 2022, more than 500 million people were infected and 6,2 million died as a result of this disease, increasingly associated with changes in human hemostasis, such as hypercoagulation. Numerous factors contribute to the hypercoagulable state, and endothelial dysfunction is the main one, since the activation of these cells can strongly activate platelets and the coagulation system.

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Cell adhesion and migration are crucial for cancer progression and malignancy. Drugs available for the treatment of metastatic melanoma are expensive and unfit for certain patients. Therefore, there is still a need to identify new drugs that block tumor cell development.

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Tuberculosis is one of the deadliest infectious diseases and a huge healthcare burden in many countries. New vaccines, including recombinant BCG-based candidates, are currently under evaluation in clinical trials. Our group previously showed that a recombinant BCG expressing LTAK63 (rBCG-LTAK63), a genetically detoxified subunit A of heat-labile toxin (LT) from , induces improved protection against () in mouse models.

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We determined the phytochemical composition, anti-inflammatory mechanism of action, ROS/RNS scavenging capacity and systemic toxicity of a purified subfraction (S8) of . The composition of S8 was assessed by LC-ESI-QTOF-MS; the anti-inflammatory activity in RAW264.7 macrophages through NF-κB activation and biomarkers by multiplex in THP-1 cells; neutrophil migration, intravital microscopy and ICAM-1 expression in mice; NETs formation and CD11b expression; S8 scavenging capacity of ROS/RNS; toxicity in larvae model.

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The new outbreak of coronavirus disease 2019 (COVID-19) has infected and caused the death of millions of people worldwide. Intensive efforts are underway around the world to establish effective treatments. Immunoglobulin from immunized animals or plasma from convalescent patients might constitute a specific treatment to guarantee the neutralization of the virus in the early stages of infection, especially in patients with risk factors and a high probability of progressing to severe disease.

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Article Synopsis
  • * The immunosensor employs 50-nm gold nanoparticles (AuNPs) attached to antibodies targeting the SARS-CoV-2 spike protein, with various spectroscopic methods confirming its effectiveness.
  • * This method shows a high level of specificity, demonstrating no response to influenza viruses, and suggests potential for broader applications in other detection technologies for affordable mass COVID-19 testing.
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  • * A new model using a glycated extracellular matrix (ECM-GC) combined with human sensory-like neurons was developed to screen for pain-relief compounds, confirming neuronal markers and the activation of pain-related genetic expressions.
  • * The study found that ECM-GC increased substance P release, a neuropeptide linked to pain, but morphine effectively reduced this release, indicating the potential of this model for testing analgesic treatments.
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Hemostatic disorders are caused either by platelet-related dysfunctions, defective blood coagulation, or by a combination of both, leading to an increased susceptibility to cardiovascular diseases (CVD) and other related illnesses. The unique specificity of anticoagulants from hematophagous arthropods, such as ticks, suggests that tick saliva holds great promise for discovering new treatments for these life-threatening diseases. In this study, we combined in silico and in vitro analyses to characterize the first recombinant serpin, herein called Dromaserpin, from the sialotranscriptome of the tick.

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Cathepsin L (CatL) is a lysosomal cysteine protease primarily involved in the terminal degradation of intracellular and endocytosed proteins. More specifically, in humans, CatL has been implicated in cancer progression and metastasis, as well as coronary artery diseases and others. Given this, the search for potent CatL inhibitors is of great importance.

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  • The text honors the Butantan Institute on its 120th anniversary by highlighting its research on envenoming in Brazil, where over 42,000 caterpillar-related accidents occur annually.
  • It emphasizes the establishment of new toxinology research centers at Butantan and the production of an antilonomic serum (ALS) to address public health needs.
  • Additionally, the study of bristle extract revealed new molecules with unique properties, potentially paving the way for innovative drugs targeting cell regeneration and inflammatory conditions.
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Article Synopsis
  • Envenomation from contact with caterpillar bristles causes severe pain, systemic inflammatory reactions, and can lead to serious health issues, including death, although the immune response specifics are not well understood.
  • The study focused on how venom affects THP-1-derived macrophages, examining its cytotoxic effects and the inflammatory markers and cytokines it triggers.
  • Findings revealed that venom activates the NF-κB pathway in macrophages, leading to increased expression of certain markers and a release of various pro-inflammatory substances, highlighting macrophages' crucial role in the inflammatory response to caterpillar envenomation.
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  • Pararamosis is a disease caused by contact with the hairs of the Brazilian moth, leading to joint inflammation and cartilage damage that mimics conditions like osteoarthritis and rheumatoid arthritis.
  • The study investigated the toxic effects of caterpillar hair extract on human chondrocytes, focusing on inflammatory markers like cytokines and matrix metalloproteinases (MMPs), using techniques like RT-qPCR and RNA-seq.
  • Results showed increased levels of inflammatory proteins and a decrease in cartilage components, indicating a significant impact of the hair extract on cartilage health and suggesting potential pathways for treating the inflammatory response associated with this disease.
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Breast cancer is the most common malignant tumor among women worldwide, and triple-negative breast cancer is the most aggressive type of breast cancer, which does not respond to hormonal therapies. The protease inhibitor, EcTI, extracted from seeds of Enterolobium contortisiliquum, acts on the main signaling pathways of the MDA-MB-231 triple-negative breast cancer cells. This inhibitor, when bound to collagen I of the extracellular matrix, triggers a series of pathways capable of decreasing the viability, adhesion, migration, and invasion of these cells.

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We have investigated Amblyomin-X-treated horse melanomas to better understand its mode of action through transcriptome analysis and the in vivo model. Amblyomin-X is a Kunitz-type homologous protein that selectively leads to the death of tumor cells via ER stress and apoptosis, currently under investigation as a new drug candidate for cancer treatment. Melanomas are immunogenic tumors, and a better understanding of the immune responses is warranted.

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Non-coding RNAs (ncRNAs) comprise a diversity of RNA species, which do not have the potential to encode proteins. Non-coding RNAs include two classes of RNAs, namely: short regulatory ncRNAs and long non-coding RNAs (lncRNAs). The short regulatory RNAs, containing up to 200 nucleotides, include small RNAs, such as microRNAs (miRNA), short interfering RNAs (siRNAs), piwi-interacting RNAs (piRNAs), and small nucleolar RNAs (snoRNAs).

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