Publications by authors named "Yasuhiro Kinugawa"

IgG4-related disease (IgG4-RD) is an autoimmune disease of unknown cause. is a transcription factor involved in immune responses, and its dysfunction leads to uncontrolled immune responses. We performed, to our knowledge, the first methylation analysis in type 1 autoimmune pancreatitis (denoted simply as AIP), a representative IgG4-RD.

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  • The study focuses on ARL4C, a protein highly expressed in colorectal cancer (CRC), which is linked to increased cell mobility, invasion, and growth.
  • Using a sensitive RNA detection method, researchers found that ARL4C was more prominently expressed at the invasion front of tumors and significantly associated with aggressive features like high-grade tumor budding and the epithelial-to-mesenchymal transition (EMT) phenotype.
  • The findings suggest that higher levels of ARL4C in both cancer cells and stromal cells may indicate a poorer prognosis for CRC patients, highlighting the need for further research on ARL4C's role in cancer progression.
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  • IgG4-positive plasma cells are found in increased numbers within the tumor microenvironment of various cancers, indicating a poor prognosis, but their role in intrahepatic cholangiocarcinoma (ICC) has not been thoroughly examined.
  • This study analyzed 37 ICC patients who underwent surgery, assessing the presence of IgG and IgG4-positive plasma cells in different tumor regions, finding a strong correlation between high IgG4 presence in the invasion front and poor overall survival rates.
  • The research concludes that high levels of IgG4 expression and the IgG4/IgG ratio serve as independent indicators of poor prognosis in ICC patients, suggesting that targeted IgG4 therapies could potentially enhance patient outcomes.
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  • LGR6 is a receptor linked to cancer progression, specifically studied in esophageal squamous cell carcinoma (ESCC) using RNAscope, a precise RNA detection method.
  • In a study involving 41 ESCC cases, 37 showed LGR6 expression, with higher levels in aggressive tumors and those treated with neoadjuvant chemotherapy.
  • High levels of LGR6 expression correlate with poorer patient prognosis, suggesting its potential as a prognostic indicator and a target for future therapies in ESCC.
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Leucine-rich repeat-containing G-protein-coupled receptor 5 (LGR5) is a known cancer stem cell marker. However, there are no reported analyses of LGR5 mRNA expression in normal liver and liver cancer tissues. Here, we evaluated LGR5 expression by RNAscope, a newly developed RNA in situ hybridization technique, using a tissue microarray consisting of 25 samples of intrahepatic cholangiocarcinoma (ICC) selected from the medical archives at our hospital.

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Background: Leucine-rich repeat-containing G-protein-coupled receptor 5 (LGR5) is a strong cancer stem cell marker in colorectal cancer; however, there are many unclear aspects of LGR5 expression in pancreatic cancer. It has been reported that the interaction between tumor cells and stroma at the fat infiltration site has a significant effect on pancreatic cancer prognosis. Therefore, we report a clinicopathological study of LGR5 expression at the fat invasion front in pancreatic cancer.

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Background: Pancreaticobiliary maljunction (PBM) is a condition characterized by chronic inflammation due to refluxed pancreatic juice into the biliary tract that is associated with an elevated risk of biliary tract cancer. DNA double-strand breaks (DSBs) are considered the most serious form of DNA damage. DSBs are provoked by inflammatory cell damage and are recognized as an important oncogenic event in several cancers.

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Background: It is difficult to distinguish between multicentric Castleman's disease (MCD) and IgG4-related lung disease (IgG4-LD), an IgG4-related disease (IgG4-RD) in the lung.

Methods: We focused on IL-6, which is elevated in MCD, to distinguish between MCD and IgG4-LD by RNAscope, a highly sensitive RNA in situ method. Six cases of MCD and four cases of IgG4-LD were selected.

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Background: LGR5 is a promising stem cell marker in gastric pylorus, but there are few reports on its expression in human gastric corpus.

Aims: To investigate the involvement of LGR5 expression in gastric corpus ulcer regeneration in humans.

Methods: LGR5 expression was analyzed in five post-ESD ulcers during the healing process of regenerating epithelial cells of the gastric corpus.

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Background: Leucine-rich repeat-containing G-protein-coupled receptor 5 (LGR5) is an important cancer stem cell marker in gastric cancer. However, no detailed studies are available on LGR5 expression in poorly differentiated gastric adenocarcinoma (PD-AC). Therefore, we investigated the relationship between LGR5 expression and clinicopathological data in PD-AC.

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  • Claudin 18 (CLDN18) is a cell surface protein involved in cell adhesion, with its isoform CLDN18.2 being highly expressed in gastric cancers, leading to the development of zolbetuximab for treating CLDN18.2-positive gastro-oesophageal adenocarcinoma.
  • A study was conducted on 56 colitis-associated colorectal adenocarcinomas (CACs), revealing that 27% expressed CLDN18, which is significantly higher compared to only 5% in sporadic colorectal cancers, with a correlation to lymph node metastasis.
  • The findings indicate that some CACs might be suitable for treatment with zolbetuximab, while only 4% showed HER2
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LGR5 is expressed in various tumors and has been identified as a putative intestinal stem cell marker. Here we investigated LGR5 expression in colorectal neuroendocrine neoplasms and analyzed the correlation with pathological characteristics. We evaluated the clinicopathological features of 8 neuroendocrine tumor (NET) grade 1 (NET G1), 4 NET Grade 2 (NET G2), and 8 NET Grade 3 (NET G3; also termed neuroendocrine carcinoma, or NEC) cases.

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  • The study investigates the connection between abnormal methylation of the SKI gene and autoimmune pancreatitis (AIP), a type of IgG4-related disease, using various analysis techniques.
  • Findings show that SKI methylation is lower in AIP compared to cases of pancreatic ductal adenocarcinoma (PDA) and normal pancreas tissues, with higher expression levels in AIP.
  • A significant correlation is noted between SKI methylation levels, IgG4 serum concentrations, and SKI expression, suggesting SKI may play a role in AIP pathogenesis, although its exact function remains unclear.
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Objectives: Autoimmune pancreatitis (AIP) is a representative IgG4-related and inflammatory disease of unknown etiology. To clarify mechanisms of carcinogenesis resulting from AIP, we focused on methylation abnormalities and KRAS mutations in AIP.

Methods: Six tumor suppressor genes (NPTX2, Cyclin D2, FOXE1, TFPI2, ppENK, and p16) that exhibited hypermethylation in pancreatic carcinoma were selected for quantitative SYBR green methylation-specific polymerase chain reaction in 10 AIP specimens, 10 pancreatic adenocarcinoma cases without history of AIP containing carcinoma areas (CAs) and noncarcinoma areas (NCAs), and 11 normal pancreas (NP) samples.

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