Publications by authors named "Yoshiki Hayashi"

S-adenosylmethionine (SAM) is the major cellular methyl donor and regulates gene expression through epigenetic and other methylation-related processes. While SAM biosynthesis influences a variety of biological phenomena including aging and disease, its cell type-specific regulation and functional implications remain poorly understood. In this study, we report that the Drosophila germline exhibits a uniquely repressive SAM biosynthesis status during gametogenesis, as indicated by low expression of SAM synthetase (Sam-S), a key enzyme for SAM production.

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Introduction: The safety of administering immune checkpoint inhibitors (ICIs) after talc pleurodesis, particularly the impact of talc on the development of immune-related interstitial lung disease (ILD), remains unclear.

Methods: We retrospectively analysed patients with primary lung cancer or malignant pleural mesothelioma who received ICIs within 90 days of talc pleurodesis at facilities participating in the Niigata Lung Cancer Treatment Study Group between November 2016 and June 2023.

Results: A total of 52 cases were included, with 17 patients (32.

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Hematogenous metastasis, a hallmark of cancer cells, involves a complex series of migration steps, including intravasation, circulation, arrest in blood vessels, and trans-endothelial migration (TEM)-the lattar two collectively referred to as extravasation. Among these steps, extravasation poses significant challenges for imaging in amniotes such as humans and mice due to its unpredictable timing and location, which limits our understanding of the underlying cellular and molecular mechanisms. Thus, the development of a novel cancer carrier model with high-resolution imaging capabilities in amniotes is essential.

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Background: Histone post-translational modification (PTM) is an important epigenomic regulation content and an essential process regulating gene expression. Histone lysine lactylation is the newly identified histone PTM that utilizes the lactyl moiety for its modification. Although histone lysine lactylation is considered an essential outcome of the Wardburg effects and the interconnection between cellular metabolism and gene regulation, the developmental contexts involving this PTM are largely unknown.

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Avian species are essential resources for human society, with their preservation and utilization heavily dependent on primordial germ cells (PGCs). However, efficient methods for isolating live PGCs from embryos remain elusive in avian species beyond chickens, and even in chickens, existing techniques have shown limited efficiency. In this study, we present a rapid, simple, and cost-effective method for labeling and sorting circulating-stage PGCs across various avian species, including Carinatae and Ratitae, using Lycopersicon Esculentum (Tomato) lectin (LEL).

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Heparan sulfate proteoglycans (HSPGs) are composed of a core protein and glycosaminoglycan (GAG) chains and serve as coreceptors for many growth factors and morphogens. To understand the molecular mechanisms by which HSPGs regulate morphogen gradient formation and signaling, it is important to determine the relative contributions of the carbohydrate and protein moieties to the proteoglycan function. To address this question, we generated ΔGAG alleles for dally and dally-like protein (dlp), two Drosophila HSPGs of the glypican family, in which all GAG-attachment serine residues are substituted to alanine residues using CRISPR/Cas9 mutagenesis.

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Article Synopsis
  • Type 1 Bartter syndrome is characterized by low potassium levels and metabolic alkalosis due to mutations in the SLC12A1 gene, while hypocalcemia is typically rare except in type 5.
  • Two siblings with type 1 Bartter syndrome exhibited recurrent severe hypocalcemia, presenting symptoms like numbness and shortness of breath after physical stress.
  • Their severe hypocalcemia was reversible with treatment, and it was found that they were in a parathyroid hormone (PTH)-resistant state, indicating that PTH resistance combined with stress might lead to unnoticed severe hypocalcemia in Type 1 and 2 Bartter syndrome patients.
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MgtE is a Mg -selective channel regulated by the intracellular Mg concentration. MgtE family proteins are highly conserved in all domains of life and contribute to cellular Mg homeostasis. In humans, mutations in the SLC41 proteins, the eukaryotic counterparts of the bacterial MgtE, are known to be associated with various diseases.

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Article Synopsis
  • The study investigates the effectiveness and safety of amrubicin (AMR) therapy in patients with recurrent small cell lung cancer (SCLC) following treatment with immune checkpoint inhibitors (ICIs) and chemotherapy.
  • A total of 30 patients were analyzed, with median progression-free survival of 3.8 months and overall survival of 10 months; results were similar regardless of cancer sensitivity to prior treatments.
  • The most frequent serious side effect was severe neutropenia, affecting 73% of patients, leading to two cases of treatment discontinuation due to adverse effects.
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The evolution of the biphasic life cycle in marine invertebrates has attracted considerable interest in zoology. We recently provided evidence that retinoic acid (RA) is involved in the regulation of metamorphosis in starfish. It also functions in life cycle transitions of jellyfish (cnidaria).

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Peripherally inserted central venous catheters (PICCs) have a potential advantage in preventing central line-associated bloodstream infection (CLABSI) compared with the centrally inserted ones (CICCs). However, due to a limited number of studies with insufficient statistical evaluation, the superiority of PICCs is difficult to be generalized in adult hematology unit. We conducted a single-center retrospective study and compared the risk of CLABSI between 472 CICCs and 557 PICCs inserted in adult patients with hematological disorders through conventional multivariate models and a propensity score-adjusted analysis.

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Magnesium is an important nutrient for plants, but much is still unknown about plant Mg2+ transporters. Combining with the structural prediction of AlphaFold2, we used mutagenesis and 28Mg uptake assay to study the highly conserved "GMN" motif of Arabidopsis thaliana MRS2-1 (AtMRS2-1) transporter. We demonstrated that the glycine and methionine in GMN motif are essential for AtMRS2-1 to transport Mg2+.

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Article Synopsis
  • * Conducted across multiple centers in Japan, the study involved 194 patients, finding a 90.8% rebiopsy implementation rate and varying success rates based on the type of biopsy: histology (81.3%), cytology (66.7%), and liquid biopsy (43.8%).
  • * Both histological and cytological samples showed a strong agreement (90.9%) in detecting the T790M mutation, suggesting that rebiopsy can enhance mutation detection and inform better treatment decisions.
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Tissue aging is a major cause of aging-related disabilities and a shortened life span. Understanding how tissue aging progresses and identifying the factors underlying tissue aging are crucial; however, the mechanism of tissue aging is not fully understood. Here we show that the biosynthesis of S-adenosyl-methionine (SAM), the major cellular donor of methyl group for methylation modifications, potently accelerates the aging-related defects during Drosophila oogenesis.

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Although diffuse large B-cell lymphoma (DLBCL) occasionally lacks surface immunoglobulin light chain restriction (iLCR) on flow cytometry (FCM), little evidence is available for iLCR-negative DLBCL. We retrospectively compared clinicopathological features of iLCR-positive and iLCR-negative DLBCL diagnosed at our institute between April 2007 and March 2018. iLCR-positive was defined as a κ/λ ratio less than 0.

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Although effective combination of antiretroviral medications is being developed, the incidence of non-Hodgkin lymphoma (NHL) with human immunodeficiency/acquired immunodeficiency syndrome (HIV/AIDS) still remains significantly higher than that in individuals without infection. Primary cardiac lymphoma (PCL) is an NHL that involves the heart and/or the pericardium. PCL is very rare and often causes serious complications, which can be a diagnostic challenge.

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Article Synopsis
  • A 70-year-old man with a history of asthma and chronic sinusitis presented with severe symptoms including fever, limb numbness, blood in urine, and gastrointestinal bleeding, alongside abnormal blood results indicating eosinophilia and elevated IgG4 levels.
  • Diagnostic procedures showed significant airway lesions and inflammation, leading to a diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA), and the patient was initially treated with steroids, which improved his condition.
  • However, after 18 months, the patient's symptoms and eosinophil levels worsened, prompting treatment with an anti-IL-5 antibody (mepolizumab), which successfully normalized his blood results and alleviated symptoms, highlighting the
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The Drosophila female germline stem cell (GSC) niche provides an excellent model for understanding the stem cell niche in vivo. The GSC niche is composed of stromal cells that provide growth factors for the maintenance of GSCs and the associated extracellular matrix (ECM). Although the function of stromal cells/growth factors has been well studied, the function of the ECM in the GSC niche is largely unknown.

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Treatment of patients with malignancy sometimes be delayed due to various reasons. Several studies revealed that an influence of diagnosis-to-treatment interval (DTI) on outcomes differs depending on the type of malignancy. In this study, we evaluated the influence of DTI on clinical outcomes in newly diagnosed patients with diffuse large B-cell lymphoma (DLBCL).

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Hermaphroditic invertebrates and plants have a self-recognition system on the cell surface of sperm and eggs, which prevents their self-fusion and enhances non-self-fusion, thereby contributing to genetic variation. However, the system of sperm-egg recognition in mammals is under debate. To address this issue, we explored the role of major histocompatibility complex class I (MHC class I, also known as histocompatibility 2-K or H2-K and H2-D in mice) antigens by analyzing () triple-knockout () male mice with full fertility.

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Donor cell-derived hematological disorder (DCHD) is a rare complication of allogeneic hematopoietic stem cell transplantation (HSCT). The number of reports of DCHD has been increasing in the last decade, which likely reflects the growing number of HSCTs and the improved ability to identify the donor cell origin. Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired hematological disorder arising in the context of clonal expansion of hematopoietic stem cells harboring a somatic mutation in phosphatidylinositol glycan anchor biosynthesis, class A.

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Allogeneic peripheral blood stem cell transplantation (PBSCT) is associated with an increased risk of severe acute and chronic graft-versus-host disease (GVHD) compared to bone marrow transplantation. Anti-thymocyte globulin (ATG) can reduce severe acute and chronic GVHD in PBSCT; however, an optimal dose of ATG remains undefined. We conducted a multicenter phase II study to investigate safety and efficacy of low-dose ATG (a total of 2 mg/kg Thymoglobulin) in patients undergoing HLA-matched PBSCT after myeloablative conditioning.

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Hyperviscosity syndrome (HVS) can cause multiple organ damage if not treated immediately. IgM multiple myeloma (IgM MM) is a very rare form of myeloma with clinical features such as elevated serum IgM, and anemia, that resemble Waldenström macroglobulinemia (WM). Distinguishing between these two diseases is important, but can be a challenging problem.

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