Publications by authors named "Buzdin A"

Background: Immune checkpoint inhibitors (ICIs) treatment have shown high efficacy for about 15 cancer types. However, this therapy is only effective in 20-30% of cancer patients. Thus, the precise biomarkers of ICI response are an urgent need.

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The metabolism of zinc and manganese plays a pivotal role in cancer progression by mediating cancer cell growth and metastasis. The SLC30A family proteins and mediate the efflux of zinc, manganese, and probably other transition element ions outside the cytoplasm to the extracellular space or into intracellular membrane compartments. The SLC39A family members and are their functional antagonists that transfer these ions into the cytoplasm.

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Background: In clinical practice, various methods are used to identify gene rearrangements in tumor samples, ranging from "classic" techniques, such as IHC, FISH, and RT-qPCR, to more advanced highly multiplexed approaches, such as NanoString technology and NGS panels. Each of these methods has its own advantages and disadvantages, but they share the drawback of detecting only a restricted (although sometimes quite extensive) set of preselected biomarkers. At the same time, whole transcriptome sequencing (WTS, RNAseq) can, in principle, be used to detect gene fusions while simultaneously analyzing an incomparably wide range of tumor characteristics.

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Inorganic polyphosphates and respective metabolic pathways and enzymes are important factors for yeast active growth in unfavorable conditions. However, particular proteins of polyphosphate metabolism remain poorly explored in this context. Here we report biochemical and transcriptomic characterization of the CRN/PPN2 yeast strain (derived from Ppn1-lacking CRN strain) overexpressing poorly studied Ppn2 polyphosphatase.

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Background: Glioblastoma (GBM) is the most aggressive and lethal central nervous system (CNS) tumor. The treatment strategy is mainly surgery and/or radiation therapy, both combined with adjuvant temozolomide (TMZ) chemotherapy. Historically, methylation of gene promoter is used as the major biomarker predicting individual tumor response to TMZ.

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Introduction: The differential ratio of nonsynonymous to synonymous nucleotide substitutions (dN/dS) is a common measure of the rate of structural evolution in proteincoding genes. In addition, we recently suggested that the proportion of transposable elements in gene promoters that host functional genomic sites serves as a marker of the rate of regulatory evolution of genes. Such functional genomic regions may include transcription factor binding sites and modified histone binding loci.

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Article Synopsis
  • - Taxanes, like paclitaxel and docetaxel, are key treatments for breast cancer, but how they work and why some patients resist them aren’t fully understood.
  • - This study analyzed a huge amount of breast cancer gene expression data to identify 34 genes and 29 pathways that can help distinguish between patients who respond well to taxane treatment and those who don’t.
  • - They developed predictive signatures based on gene expression and pathway activation that showed strong potential in identifying treatment responses, indicating a promising step towards more personalized breast cancer therapy.
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Recently, the use of circularly polarized radiation for on-demand switching between distinct quantum states in a superconducting nanoring exposed to half-quantum magnetic flux has been proposed. However, the effectiveness of this method depends on the system's stability against local variations in the superconducting characteristics of the ring and flux fluctuations. In this study, we utilize numerical simulations based on the time-dependent Ginzburg-Landau equation to evaluate the influence of these inevitable factors on the switching behavior.

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Article Synopsis
  • Despite significant investment and effort over the past 52 years in the "War on Cancer," traditional treatment methods like chemotherapy and radiation have fallen short of expectations.
  • A new approach proposes targeting cancer-stromal synapses, the connections between cancer cells and their surrounding microenvironment, which could lead to more effective treatment.
  • This method aims to disrupt these synapses using targeted chemical agents, potentially enhancing treatment safety, precision, and reducing the likelihood of drug resistance.
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  • Dual inhibitors like lapatinib are effective for treating HER2-positive breast cancer, but their efficacy can be diminished by human serum and EGF.
  • A study on the SK-BR-3 breast cancer cell line showed that lapatinib treatment changed the expression of 350 proteins, and combining it with serum or EGF reversed much of this change, negating growth inhibition.
  • The research found that lapatinib increased proteins related to mitochondrial function and cellular respiration, marking enhanced respiration as a new mechanism of action for lapatinib in targeting HER2-positive cancer cells.
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Cancer chimeric, or fusion, transcripts are thought to most frequently appear due to chromosomal aberrations that combine moieties of unrelated normal genes. When being expressed, this results in chimeric RNAs having upstream and downstream parts relatively to the breakpoint position for the 5'- and 3'-fusion components, respectively. As many other types of cancer mutations, fusion genes can be of either driver or passenger type.

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Objective: The purpose of this study was to investigate the relationship of soil pollution factors such as heavy metal ions with the incidence of cancer in the Kyzylorda region of Kazakhstan.

Methods: Concentrations of heavy metal ions in the soils of different sites of Kyzylorda region, Kazakhstan, were sampled and correlated with incidence of cancer in 2021.

Results: Chromium content in the soil exceeded maximum permissible concentration (MPC) in the samples for all sites except Kazaly and Shieli, and the highest excess of 2.

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The gene encodes the reverse transcriptase subunit of telomerase and is normally transcriptionally suppressed in differentiated human cells but reactivated in cancers where its expression is frequently associated with poor survival prognosis. Here we experimentally assessed the RNA sequencing expression patterns associated with transcription in 1039 human cancer samples of 27 tumor types. We observed a bimodal distribution of expression where ∼27% of cancer samples did not express and the rest showed a bell-shaped distribution.

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Identification of genes and molecular pathways with congruent profiles in the proteomic and transcriptomic datasets may result in the discovery of promising transcriptomic biomarkers that would be more relevant to phenotypic changes. In this study, we conducted comparative analysis of 943 paired RNA and proteomic profiles obtained for the same samples of seven human cancer types from The Cancer Genome Atlas (TCGA) and NCI Clinical Proteomic Tumor Analysis Consortium (CPTAC) [two major open human cancer proteomic and transcriptomic databases] that included 15,112 protein-coding genes and 1611 molecular pathways. Overall, our findings demonstrated statistically significant improvement of the congruence between RNA and proteomic profiles when performing analysis at the level of molecular pathways rather than at the level of individual gene products.

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Lapatinib is a targeted therapeutic inhibiting HER2 and EGFR proteins. It is used for the therapy of HER2-positive breast cancer, although not all the patients respond to it. Using human blood serum samples from 14 female donors (separately taken or combined), we found that human blood serum dramatically abolishes the lapatinib-mediated inhibition of growth of the human breast squamous carcinoma SK-BR-3 cell line.

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We suggest a theoretical description of the photogalvanic phenomena arising in superconducting condensates in the field of electromagnetic wave. The ac Hall effect and photon drag are shown to originate from the second-order nonlinear response of superconducting carriers caused by the suppression of their concentration due to the combined influence of the electron-hole asymmetry and charge imbalance generated by the incident electromagnetic wave. Starting from the time-dependent Ginzburg-Landau theory with the complex relaxation constant, we develop a phenomenological description of these phenomena and investigate the resulting behavior of the dc supercurrent and second harmonic induced by microwave radiation incident on a superconductor surface.

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Members of the EGFR family of tyrosine kinase receptors are major regulators of cellular proliferation, differentiation, and survival. In humans, abnormal activation of EGFR is associated with the development and progression of many cancer types, which makes it an attractive target for molecular-guided therapy. Two classes of EGFR-targeted cancer therapeutics include monoclonal antibodies (mAbs), which bind to the extracellular domain of EGFR, and tyrosine kinase inhibitors (TKIs), which mostly target the intracellular part of EGFR and inhibit its activity in molecular signaling.

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Individual gene expression and molecular pathway activation profiles were shown to be effective biomarkers in many cancers. Here, we used the human interactome model to algorithmically build 7470 molecular pathways centered around individual gene products. We assessed their associations with tumor type and survival in comparison with the previous generation of molecular pathway biomarkers (3022 "classical" pathways) and with the RNA transcripts or proteomic profiles of individual genes, for 8141 and 1117 samples, respectively.

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Co-normalization of RNA profiles obtained using different experimental platforms and protocols opens avenue for comprehensive comparison of relevant features like differentially expressed genes associated with disease. Currently, most of bioinformatic tools enable normalization in a flexible format that depends on the individual datasets under analysis. Thus, the output data of such normalizations will be poorly compatible with each other.

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Article Synopsis
  • Normal tissues are crucial for studying gene expression related to diseases, but healthy controls are often obtained only post-mortem, leading researchers to use "normal" tissues next to tumors as controls.
  • A study compared gene expression profiles in tumor-adjacent tissues to those from autopsy-derived healthy tissues, discovering significant differences linked to immune activation, cell signaling pathways, and structural changes.
  • Using a macaque model, researchers identified RNA degradation in lung samples that affected gene expression results, emphasizing the need to consider sample quality and handling in research protocols.
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Regardless of the presence or absence of specific diagnostic mutations, many cancer patients fail to respond to EGFR-targeted therapeutics, and a personalized approach is needed to identify putative (non)responders. We found previously that human peripheral blood and EGF can modulate the activities of EGFR-specific drugs on inhibiting clonogenity in model EGFR-positive A431 squamous carcinoma cells. Here, we report that human serum can dramatically abolish the cell growth rate inhibition by EGFR-specific drugs cetuximab and erlotinib.

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Magneto-optical imaging of quantized magnetic flux tubes in superconductors - Abrikosov vortices - is based on Faraday rotation of light polarization within a magneto-optical indicator placed on top of the superconductor. Due to severe aberrations induced by the thick indicator substrate, the spatial resolution of vortices is usually well beyond the optical diffraction limit. Using a high refractive index solid immersion lens placed onto the indicator garnet substrate, we demonstrate wide field optical imaging of single flux quanta in a Niobium film with a resolution better than 600 nm and sub-second acquisition periods, paving the way to high-precision and fast vortex manipulation.

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The diverse cell types of an organ have a highly structured organization to enable their efficient and correct function. To fully appreciate gene functions in a given cell type, one needs to understand how much, when and where the gene is expressed. Classic bulk RNA sequencing and popular single cell sequencing destroy cell structural organization and fail to provide spatial information.

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