Publications by authors named "Ali Zari"

Article Synopsis
  • Plant-based natural compounds, particularly from apricot cultivars, were studied for their potential anti-diabetic, anti-Alzheimer, and anti-cancer effects, using both qualitative and quantitative biochemical profiling.
  • High-performance liquid chromatography (HPLC) showed significant secondary metabolite content in 10 apricot cultivars, with extracts particularly inhibiting breast cancer cells (MCF-7).
  • Correlation and statistical analyses revealed strong relationships among bioactive compounds, with specific cultivars like 'Irani' and 'Tilton' standing out for their high levels of beneficial compounds, indicating their potential therapeutic value.
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Background: The histone variant macroH2A (mH2A), the most deviant variant, is about threefold larger than the conventional histone H2A and consists of a histone H2A-like domain fused to a large Non-Histone Region responsible for recruiting PARP-1 to chromatin. The available data suggest that the histone variant mH2A participates in the regulation of transcription, maintenance of heterochromatin, NAD metabolism, and double-strand DNA repair.

Results: Here, we describe a novel function of mH2A, namely its implication in DNA oxidative damage repair through PARP-1.

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DNA methylation is one of the most important epigenetic mark involved in many physiologic cellular processes and pathologies. During mitosis, the transmission of DNA methylation patterns from a mother to the daughter cells is ensured through the action of the Ubiquitin-like, containing PHD and RING domains, 1/DNA methyltransferase 1 (UHRF1/DNMT1) tandem. UHRF1 is involved in the silencing of many tumor suppressor genes (TSGs) via mechanisms that remain largely to be deciphered.

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HIRIP3 is a mammalian protein homologous to the yeast H2A.Z deposition chaperone Chz1. However, the structural basis underlying Chz's binding preference for H2A.

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Article Synopsis
  • Multiple myeloma (MM) is a serious disease characterized by abnormal plasma cell growth and high mortality rates, prompting research for effective treatments.
  • A study investigated 100 natural ingredients for their ability to inhibit the IgH enzyme linked to MM, identifying Diospyrin and Parviflorone F as notable inhibitors, with Parviflorone F showing better binding stability in simulations.
  • Ultimately, Parviflorone F was recognized as a strong potential inhibitor of the IgH domain, warranting further research into its therapeutic applications for MM.
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Article Synopsis
  • Inherited defects in the MBD4 gene increase the risk for adenomatous polyposis and colorectal cancer by causing a specific type of DNA damage known as C > T transitions.
  • Research shows that MBD4 plays a crucial role in maintaining DNA methylation and repairing G/T mismatches, with its absence leading to widespread hypomethylation and transcriptional changes in genes and repetitive elements.
  • The study concludes that MBD4 is essential for correcting deaminated 5-methylcytosines, highlighting its importance in protecting DNA from methylation-related damage in both healthy and diseased states.
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Background: Tyrosine-protein kinase Fyn (Fyn) is a critical signaling molecule involved in various cellular processes, including neuronal development, synaptic plasticity, and disease pathogenesis. Dysregulation of Fyn kinase has been implicated in various complex diseases, including neurodegenerative disorders such as Alzheimer's and Parkinson's diseases, as well as different cancer types. Therefore, identifying small molecule inhibitors that can inhibit Fyn activity holds substantial significance in drug discovery.

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Breast cancer (BC) is one of the most widespread types of cancer affecting females, and therefore, early diagnosis is critical. BC is a complex heterogeneous disease affected by several key pathways. Among these, WNT proteins and their frizzled receptors (FZD) have been demonstrated to be crucial in regulating a number of cellular and molecular events in BC tumorigenesis.

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: Colchicine has been proposed as a cytokine storm-blocking agent for COVID-19 due to its efficacy as an anti-inflammatory drug. The findings of the studies were contentious on the role of colchicine in preventing deterioration in COVID-19 patients. We aimed to evaluate the efficacy of colchicine in COVID-19-hospitalized patients.

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Alterations to the EGFR (epidermal growth factor receptor) gene, which primarily occur in the axon 18-21 position, have been linked to a variety of cancers, including ovarian, breast, colon, and lung cancer. The use of TK inhibitors (gefitinib, erlotinib, lapatinib, and afatinib) and monoclonal antibodies (cetuximab, panitumumab, and matuzumab) in the treatment of advanced-stage cancer is very common. These drugs are becoming less effective in EGFR targeted cancer treatment and developing resistance to cancer cell eradication, which sometimes necessitates stopping treatment due to the side effects.

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Aptamers, the nucleic acid analogs of antibodies, bind to their target molecules with remarkable specificity and sensitivity, making them promising diagnostic and therapeutic tools. The systematic evolution of ligands by exponential enrichment (SELEX) is time-consuming and expensive. However, regardless of those issues, it is the most used in vitro method for selecting aptamers.

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The current study was conducted to examine the in vitro anticancer potential of (bark, leaves, pulp and seed). The plant material was collected from UT of J&K and methodical bioassays were carried out on ten human cancer cell lines (Michigan Cancer Foundation-7 (MCF-7), M.D.

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Wnt signalling receptors, Frizzleds (FZDs), play a pivotal role in many cellular events during embryonic development and cancer. Female breast cancer (BC) is currently the worldwide leading incident cancer type that cause 1 in 6 cancer-related death. FZD receptors expression in cancer was shown to be associated with tumour development and patient outcomes including recurrence and survival.

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Conventional cancer treatments have shown several unfavourable adverse effects, as well as an increase in anticancer drug resistance, which worsens the impending cancer therapy. Thus, the emphasis is currently en route for natural products. There is currently great interest in the natural bioactive components from medicinal plants possessing anticancer characteristics.

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Ovarian cancer (OC) is the deadliest among all gynecological cancers. Epidemiological studies showed that obesity might influence many cancers including OC. One of the key factors that may link obesity and OC is leptin (LEP), known as an adipokine with pleiotropic effects on body homeostasis.

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is a medicinal plant native to Peru that has been traditionally used in the treatment of various inflammatory disorders. In this study, the effectiveness of as an anti-cancer agent was assessed using the growth and survival of B16-BL6 mouse melanoma cells. B16-BL6 cell cultures treated with both ethanol and phosphate-buffered saline (PBS) extracts of displayed up to 80% lower levels of growth and increased apoptosis compared to vehicle controls.

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