Publications by authors named "Timur Valiev"

Article Synopsis
  • Metastatic colorectal cancer has a low 5-year survival rate of under 15%, with common metastasis sites being the lungs and liver, while skin metastases are rare and often indicate a worse prognosis.
  • A case study of a 62-year-old woman revealed skin metastases from rectal cancer developed two years after treatment, confirming these through histological examination, although differing mutations were found between the primary tumor and skin lesions.
  • Despite treatment with FOLFOX6 chemotherapy and bevacizumab, the therapy failed, highlighting the need for close monitoring of skin for metastases in rectal cancer patients, as literature suggests median survival after detection is only 8.5 months.
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Article Synopsis
  • Diagnosing skin diseases in children is complex, and Incontinentia pigmenti (IP) is a rare hereditary condition that can lead to serious complications like squamous cell carcinoma (SCC) in young patients.
  • A case study involving a 10-year-old girl with IP highlights the importance of an interdisciplinary approach, with input from multiple specialists including dermatologists, geneticists, and oncologists.
  • Genetic evaluations confirmed a mutation in the gene responsible for IP in the family, leading to successful treatment over a 2-year period, while also revealing varied symptoms among affected family members.
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This review is focused on synephrine, the principal phytochemical found in bitter orange and other medicinal plants and widely used as a dietary supplement for weight loss/body fat reduction. We examine different aspects of synephrine biology, delving into its established and potential molecular targets, as well as its mechanisms of action. We present an overview of the origin, chemical composition, receptors, and pharmacological properties of synephrine, including its anti-inflammatory and anti-cancer activity in various in vitro and animal models.

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Objectives: To evaluate the role of ABCB1 (C3435T rs1045642, rs1128503, rs2032582, rs4148738), SLCO1B1 T521C rs4149056 genetic polymorphisms in the development of major types of methotrexate (MTX) toxicities and the occurrence of a terminal event (death, relapse) in pediatric АLL.

Methods: The study included 124 patients diagnosed with pediatric ALL. All patients treated according to the protocols of the German BFM group (2002/2009) with high-dose (1,000, 2,000 and 5,000 mg/m) methotrexate.

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Objectives: The present study investigated the analysis of adverse drug reactions (ADRs) to tamoxifen (TAM) in breast cancer patients in relation to the carriage of genetic polymorphisms of genes encoding enzymes of CYP system and transporters of P-glycoprotein (Pg) and predictive models based on it.

Methods: A total of 120 women with breast cancer taking adjuvant TAM were examined for the gene polymorphisms such as , , , , , and (). Allelic variants were determined using the real-time polymerase chain reaction method.

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Despite the achievements that have increased viability after the transplantation of allogeneic hematopoietic stem cells (aHSCT), chronic graft-versus-host disease (cGVHD) remains the main cause of late complications and post-transplant deaths. At the moment, therapy alternatives demonstrate limited effectiveness in steroid-refractory illness; in addition, we have no reliable data on the mechanism of this condition. The lack of drugs of choice for the treatment of GVHD underscores the significance of the design of new therapies.

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The potential of mesenchymal multipotent (stem) cells (MSC) to modify immune reactions and mediate hematopoiesis boosted great interest for their use in allogeneic hemopoietic stem cell transplantation. Because of MSC production of a wide range of cytokines and growth factors, these cells are included in the therapy of graft-versus-host disease (GVHD). A number of clinical studies have demonstrated safety and efficacy of MSC-based therapy in acute GVHD.

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Nijmegen breakage syndrome (NBS) is a DNA repair disorder characterized by combined immunodeficiency and a high predisposition to lymphoid malignancies. The majority of NBS patients are identified with a homozygous five base pair deletion in the ( gene (c.657_661del5, p.

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