Publications by authors named "Javad Sharifi Rad"

Didemnins, a class of cyclic depsipeptides derived from marine organisms exhibit notable anticancer properties. Among them, Didemnin B has been extensively researched for its strong antitumor activity and progression to clinical trials. Nonetheless, its clinical application has been impeded by challenges like poor bioavailability and dose-limiting toxicity.

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The p53-MDM2 pathway plays a crucial role regulating tumor suppression and is a focal point of cancer research. This literature review delves into the complex interplay between the tumor suppressor protein p53 and its main regulator MDM2, highlighting their interaction and implications in cancer development and progression. The review compiles and summarizes the existing understanding of the biology and regulation of p53 and MDM2, emphasizing their roles in various cellular processes, including cell cycle regulation, DNA repair, apoptosis, and metabolism.

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  • Cancer therapy faces issues like drug resistance and severe side effects, prompting exploration of novel, cost-effective treatments like Piper nigrum (black pepper) extract as a complementary anticancer agent.
  • Piper nigrum contains bioactive compounds such as piperine that show significant anticancer effects, including tumor inhibition and enhancing the effectiveness of traditional chemotherapy while reducing side effects.
  • The review identifies challenges such as variability and bioavailability of PNE, underscoring the need for further research to validate its use in clinical settings and improve cancer treatment outcomes.
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Diabetes mellitus (DM) prevalence is rising worldwide. Current therapies comprising subcutaneous insulin injections can cause adverse effects such as lipodystrophy, local reactions like redness and swelling, fluid retention, and allergic reactions. Nanoparticle carriers for oral insulin are groundbreaking compared to existing methods because they are non-invasive treatments, showing operational convenience, controlled release profile, and ability to simulate the physiological delivery route into the bloodstream.

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Recent research has increasingly focused on phytochemicals as promising anticancer agents, with glucosinolates (GSLs) and their hydrolytic derivatives playing a central role. These sulfur-containing compounds, found in plants of the Brassicales order, are converted by myrosinase enzymes into biologically active products, primarily isothiocyanates (ITCs) and indoles, which exhibit significant anticancer properties. Indole-3-carbinol, diindolylmethane, sulforaphane (SFN), phenethyl isothiocyanate (PEITC), benzyl isothiocyanate, and allyl isothiocyanate have shown potent anticancer effects in animal models, particularly in breast, prostate, lung, melanoma, bladder, hepatoma, and gastrointestinal cancers.

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Betulin is a bioactive compound found in large quantities in birch bark and has a triterpene pentacyclic structure. Through the oxidation of betulin, betulinic acid is obtained, which is found in large quantities in nature. Betulin and betulinic acid have multiple pharmacological properties such as antiviral, anti-inflammatory, and anticancer properties.

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Interest in biological therapy for cancer has surged due to its precise targeting of cancer cells and minimized impact on surrounding healthy tissues. This review discusses various biological cancer therapies, highlighting advanced alternatives over conventional chemotherapy alone. It explores DNA and RNA-based vaccines, T-cell modifications, adoptive cell transfer, CAR T cell therapy, angiogenesis inhibitors, and the combination of immunotherapy with chemotherapy, offering a holistic view of the potential in cancer treatment.

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  • * Recent studies highlight its pharmacological properties, particularly those of methyl antcinate A (MAA), which shows significant anti-cancer, anti-inflammatory, and gastro-protective effects.
  • * There is a need for further research and clinical trials to better understand MAA's anti-tumor effects and to explore the structure-activity relationships of antcins for potential therapeutic applications.
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  • * This study reviews methods from 2000 to 2023, focusing on how traditional knowledge combined with modern techniques, including AI, can enhance the search for bioactive compounds.
  • * The review emphasizes the historic significance of natural products, outlines current technological improvements in isolating bioactive compounds, and discusses challenges like biodiversity sustainability while suggesting innovative solutions.
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  • * Withania somnifera, or Ashwagandha, contains Withaferin A (WFA), a compound with anti-inflammatory and anti-tumor properties that shows promise against various cancers with low toxicity.
  • * WFA's anticancer mechanisms include inducing apoptosis and inhibiting key signaling pathways, showing effectiveness in preclinical studies across several cancer types; further clinical trials are needed to confirm its potential in human treatment.
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  • This study investigates the pain-relieving (analgesic) and anxiety-reducing (anxiolytic) effects of citronellal (CTL) in Swiss mice using innovative, cost-effective models.
  • Results showed that CTL significantly decreased various anxiety and pain-related behaviors in mice compared to a control group, even outperforming standard drugs like diclofenac sodium in some tests.
  • In addition, in silico studies suggested that CTL interacts with specific receptors (GABA) and enzymes (COX), indicating its potential as an effective anxiolytic and analgesic agent through these molecular pathways.
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  • Flavopiridol is a potent CDK inhibitor derived from rohitukine, known for its anticancer effects such as cell cycle arrest and apoptosis, though clinical use is limited by toxicity and drug resistance.
  • Its efficacy is influenced by structural modifications, particularly in the D ring, leading to synthetic derivatives that show improved anticancer activity.
  • Future research should prioritize enhancing flavopiridol's therapeutic profile, reducing toxicity, and exploring combination therapies, especially with immunotherapy, to overcome resistance in cancer treatment.
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Thapsigargin, a sesquiterpene lactone derived from Thapsia garganica L., has demonstrated mixed potential as an anticancer agent due to its potent ability to disrupt calcium signaling and induce apoptosis. This review evaluates the chemopreventive and chemotherapeutic potential of thapsigargin, focusing on its molecular mechanisms and toxicity.

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  • HS-1793 is a new synthetic derivative of resveratrol, known for its health benefits like anticancer and anti-inflammatory effects, but has better bioavailability than resveratrol itself.
  • * It was discovered in 2007 and has shown promising results in metabolic processes, pharmacokinetics, and pharmacodynamics.
  • * The review discusses recent research on HS-1793, assessing its efficacy and setting the stage for future clinical trials in human diseases.*
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Diosmin, a potent bioflavonoid derived from citrus fruits, has gained significant attention for its anticancer potential, reflecting a critical need in the ongoing battle against cancer. Amidst increasing cancer incidence, the quest for safer and more effective treatments has brought diosmin to the forefront, given its unique pharmacological profile distinct from other flavonoids. Diosmin's anticancer mechanisms are multifaceted, involving apoptosis induction, angiogenesis inhibition, and metastasis prevention.

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  • * It focuses on the promising anticancer properties of mangrove plants and their compounds, which have been shown to have multiple beneficial biological effects such as anti-inflammatory and antioxidant activities.
  • * The study reviews the preclinical evidence gathered from various academic sources to suggest that mangrove-derived compounds could be valuable in developing new cancer therapies through several mechanisms, including inducing cell death and inhibiting tumor growth.
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  • * This review highlights α-solanine, a plant-derived glycoalkaloid from potatoes, which shows potential anticancer properties based on extensive research over the past two decades.
  • * The study emphasizes the need for further research to enhance the efficacy and safety of α-solanine in cancer therapy while also suggesting potato peels as a sustainable source for extraction.
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Many naturally derived compounds are currently used in oncotherapy. Besides official medicine, complementary and alternative medicine practices, including old herbal remedies, are widely used and accepted as additional tools in cancer treatment. Nakai (AGN), a medicinal herb in Asia, has roots historically used in medicine.

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Anticancer drug discovery needs serious attention to overcome the high mortality rate caused by cancer. There are still many obstacles to treating this disease, such as the high cost of chemotherapeutic drugs, the resulting side effects from the drug, and the occurrence of multidrug resistance. Herbaceous plants are a reservoir of natural compounds that can be anticancer drugs with novel mechanisms of action.

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Long non-coding RNAs (lncRNAs) have been in the spotlight for the past two decades due to their extensive role in regulating a wide range of cellular processes. Development, differentiation, regulation, and modulation are some of the vital cellular cascades coordinated by these molecules. Despite their importance, there has been limited literature on their practical implications in cancer prevention.

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Camptothecin (CPT), an alkaloid isolated from the Camptotheca tree, has demonstrated significant anticancer properties in a range of malignancies. However, its therapeutic efficacy is limited by its hydrophobicity, poor bioavailability, and systemic toxicity. Derivatives, analogues, and nanoformulations of CPT have been synthesized to overcome these limitations.

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Glypican-3 (GPC-3) is predominantly found in the placenta and fetal liver, with limited expression in adult tissues. Its re-expression in hepatocellular carcinoma (HCC) and secretion into the serum highlights its potential as a diagnostic marker. GPC-3 is involved in important cellular processes such as proliferation, metastasis, apoptosis, and epithelial-mesenchymal transition through various signaling pathways including Wnt, IGF, YAP, and Hedgehog.

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  • Metabolic dysfunction-associated steatohepatitis (MASH) and its progression to hepatocellular carcinoma (HCC) are influenced by unique molecular and immune features, especially connected to the gut microbiome.
  • The "gut-liver axis" reflects the crucial interaction between the gut microbiota and the liver, impacting the development and disease progression through microbial metabolites and immune responses.
  • A literature review from various databases highlights the gut microbiota's significant role in MASH and HCC, calling for more clinical research to improve diagnostic methods and create targeted therapies to help treat liver diseases.
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For centuries, cannabinoids have been utilized for their medicinal properties, particularly in Asian and South-Asian countries. Cannabis plants, known for their psychoactive and non-psychoactive potential, were historically used for spiritual and remedial healing. However, as cannabis became predominantly a recreational drug, it faced prohibition.

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Cancer remains a major global health challenge, prompting the search for effective and less toxic treatments. Anethole, a bioactive compound found in essential oils of anise and fennel, commonly used as a food preservative, has recently garnered attention for its potential anti-cancer properties. This comprehensive review aims to systematically assess the anti-cancer effects of anethole, elucidating its mechanisms of action, pharmacokinetics, bioavailability, and synergistic potential with conventional cancer therapies.

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