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  1. Article ; Online: Histopathological diagnosis of ulcerative colitis-associated neoplasia.

    Kawachi, Hiroshi

    Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society

    2019  Volume 31 Suppl 1, Page(s) 31–35

    Abstract: In patients with ulcerative colitis, tumor development occurs with an increase in the duration of the disease. Such lesions, known as ulcerative colitis-associated neoplasia (UCAN), histologically show a broad variety of findings such as low-grade ... ...

    Abstract In patients with ulcerative colitis, tumor development occurs with an increase in the duration of the disease. Such lesions, known as ulcerative colitis-associated neoplasia (UCAN), histologically show a broad variety of findings such as low-grade dysplasia, high-grade dysplasia, and invasive carcinoma. For pathologists, however, the histopathological diagnosis of UCAN is occasionally difficult. Problems in pathological diagnosis can be summarized into the following three categories: (i) difficulty in discriminating UCAN from non-neoplastic inflammatory change; (ii) difficulty in discriminating UCAN from sporadic epithelial neoplasm; and (iii) difficulty in histological grading of UCAN. For most lesions, pathologists can make conclusive histological diagnoses without any problems. However, pathologists occasionally face diagnostic difficulties, especially in cases of lesions with borderline or indefinite histology and, therefore, at least two experienced gastrointestinal pathologists are needed to confirm the diagnosis. Hence, a confirmation is usually preferable for the estimation of tumor depth and lymphovascular invasion in digestive tract cancers as well as in UCAN. Immunohistochemistry for p53 and Ki-67 (MIB-1) is occasionally useful as an ancillary tool. Since UCAN has distinct characteristics compared to sporadic epithelial neoplasia, its treatment strategy should be carefully discussed by a multidisciplinary team, especially for cases of lesions with indefinite histology. At present, although surgical intervention such as total colectomy is the most promising procedure for UCAN, recent advances in endoscopic diagnosis and therapy are expected to improve future treatment strategy.
    MeSH term(s) Colectomy ; Colitis, Ulcerative/complications ; Colitis, Ulcerative/pathology ; Colitis, Ulcerative/therapy ; Colorectal Neoplasms/etiology ; Colorectal Neoplasms/pathology ; Colorectal Neoplasms/therapy ; Gastrointestinal Neoplasms/etiology ; Gastrointestinal Neoplasms/pathology ; Gastrointestinal Neoplasms/therapy ; Humans ; Immunohistochemistry
    Language English
    Publishing date 2019-04-17
    Publishing country Australia
    Document type Journal Article ; Review
    ZDB-ID 1171589-3
    ISSN 1443-1661 ; 0915-5635
    ISSN (online) 1443-1661
    ISSN 0915-5635
    DOI 10.1111/den.13387
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Esophageal squamous cell carcinoma darkly stained with iodine.

    Tanaka, Ippei / Fujishima, Fumiyoshi / Kawachi, Hiroshi

    Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society

    2022  Volume 35, Issue 3, Page(s) 401

    MeSH term(s) Humans ; Esophageal Squamous Cell Carcinoma ; Esophageal Neoplasms/diagnosis ; Esophageal Neoplasms/pathology ; Iodine ; Carcinoma, Squamous Cell/diagnosis ; Carcinoma, Squamous Cell/pathology
    Chemical Substances Iodine (9679TC07X4)
    Language English
    Publishing date 2022-12-15
    Publishing country Australia
    Document type Letter
    ZDB-ID 1171589-3
    ISSN 1443-1661 ; 0915-5635
    ISSN (online) 1443-1661
    ISSN 0915-5635
    DOI 10.1111/den.14488
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Clinical Evaluation of Computer-Aided Colorectal Neoplasia Detection Using a Novel Endoscopic Artificial Intelligence: A Single-Center Randomized Controlled Trial.

    Nakashima, Hirotaka / Kitazawa, Naoko / Fukuyama, Chika / Kawachi, Hiroshi / Kawahira, Hiroshi / Momma, Kumiko / Sakaki, Nobuhiro

    Digestion

    2023  Volume 104, Issue 3, Page(s) 193–201

    Abstract: Introduction: Computer-aided diagnostic systems are emerging in the field of gastrointestinal endoscopy. In this study, we assessed the clinical performance of the computer-aided detection (CADe) of colonic adenomas using a new endoscopic artificial ... ...

    Abstract Introduction: Computer-aided diagnostic systems are emerging in the field of gastrointestinal endoscopy. In this study, we assessed the clinical performance of the computer-aided detection (CADe) of colonic adenomas using a new endoscopic artificial intelligence system.
    Methods: This was a single-center prospective randomized study including 415 participants allocated into the CADe group (n = 207) and control group (n = 208). All endoscopic examinations were performed by experienced endoscopists. The performance of the CADe was assessed based on the adenoma detection rate (ADR). Additionally, we compared the adenoma miss rate for the rectosigmoid colon (AMRrs) between the groups.
    Results: The basic demographic and procedural characteristics of the CADe and control groups were as follows: mean age, 54.9 and 55.9 years; male sex, 73.9% and 69.7% of participants; and mean withdrawal time, 411.8 and 399.0 s, respectively. The ADR was 59.4% in the CADe group and 47.6% in the control group (p = 0.018). The AMRrs was 11.9% in the CADe group and 26.0% in the control group (p = 0.037).
    Conclusion: The colonoscopy with the CADe system yielded an 11.8% higher ADR than that performed by experienced endoscopists alone. Moreover, there was no need to extend the examination time or request the assistance of additional medical staff to achieve this improved effectiveness. We believe that the novel CADe system can lead to considerable advances in colorectal cancer diagnosis.
    MeSH term(s) Humans ; Male ; Middle Aged ; Artificial Intelligence ; Colonic Polyps/diagnostic imaging ; Prospective Studies ; Colonoscopy ; Colonic Neoplasms ; Adenoma/diagnostic imaging ; Computers ; Colorectal Neoplasms/diagnostic imaging
    Language English
    Publishing date 2023-01-04
    Publishing country Switzerland
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 1712-7
    ISSN 1421-9867 ; 0012-2823
    ISSN (online) 1421-9867
    ISSN 0012-2823
    DOI 10.1159/000528085
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: A rare gastric lesion: diminutive, well-differentiated, Grade 3, type 3 gastric neuroendocrine tumor with extremely high ki-67 index removed en bloc under endoscopy.

    Zhu, Chunpeng / Kawachi, Hiroshi / Lu, Xinliang

    Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association

    2022  Volume 25, Issue 3, Page(s) 659–664

    Abstract: Grade 3, type 3 gastric neuroendocrine tumor (g-NET) shows specific features of clinical interest and the therapeutic management of the lesion is not yet completely standardized. We present the unusual case of a 34-year-old male patient with a diminutive ...

    Abstract Grade 3, type 3 gastric neuroendocrine tumor (g-NET) shows specific features of clinical interest and the therapeutic management of the lesion is not yet completely standardized. We present the unusual case of a 34-year-old male patient with a diminutive (less than 0.5 cm), well-differentiated, G3, type 3g-NET with extremely high Ki-67 index (higher than 80%). The lesion was subsequently removed en bloc via endoscopic submucosal dissection. Regarding the proliferation rate, Ki-67 index values usually range from 21 to 50%, and less commonly above 55%, in G3 NET. To our knowledge, this lesion represents a small size with the highest Ki-67 index diagnosed with G3 g-NET. However, as g-NET might recur even after a long duration, we recommend a long-term follow-up, such as 10 years after complete resection in patients to evaluate the endoscopic resection approach.
    MeSH term(s) Adult ; Endoscopy, Gastrointestinal ; Gastric Mucosa/pathology ; Humans ; Intestinal Neoplasms ; Ki-67 Antigen/analysis ; Male ; Neuroendocrine Tumors/pathology ; Neuroendocrine Tumors/surgery ; Pancreatic Neoplasms ; Stomach Neoplasms/pathology ; Stomach Neoplasms/surgery
    Chemical Substances Ki-67 Antigen
    Language English
    Publishing date 2022-02-18
    Publishing country Japan
    Document type Case Reports ; Journal Article
    ZDB-ID 1463526-4
    ISSN 1436-3305 ; 1436-3291
    ISSN (online) 1436-3305
    ISSN 1436-3291
    DOI 10.1007/s10120-022-01277-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: 14-3-3 Proteins stabilize actin and vimentin filaments to maintain processes in renal glomerular podocyte.

    Yasuda, Hidenori / Fukusumi, Yoshiyasu / Zhang, Ying / Kawachi, Hiroshi

    FASEB journal : official publication of the Federation of American Societies for Experimental Biology

    2022  Volume 37, Issue 10, Page(s) e23168

    Abstract: 14-3-3 proteins are a ubiquitously expressed family of adaptor proteins. Despite exhibiting high sequence homology, several 14-3-3 isoforms have isoform-specific binding partners and roles. We reported that 14-3-3β interacts with FKBP12 and synaptopodin ... ...

    Abstract 14-3-3 proteins are a ubiquitously expressed family of adaptor proteins. Despite exhibiting high sequence homology, several 14-3-3 isoforms have isoform-specific binding partners and roles. We reported that 14-3-3β interacts with FKBP12 and synaptopodin to maintain the structure of actin fibers in podocytes. However, the precise localization and differential role of 14-3-3 isoforms in kidneys are unclear. Herein, we showed that 14-3-3β in glomeruli was restricted in podocytes, and 14-3-3σ in glomeruli was expressed in podocytes and mesangial cells. Although 14-3-3β was dominantly co-localized with FKBP12 in the foot processes, a part of 14-3-3β was co-localized with Par3 at the slit diaphragm. 14-3-3β interacted with Par3, and FKBP12 bound to 14-3-3β competitively with Par3. Deletion of 14-3-3β enhanced the interaction of Par3 with Par6 in podocytes. Gene silencing for 14-3-3β altered the structure of actin fibers and process formation. 14-3-3β and synaptopodin expression was decreased in podocyte injury models. In contrast, 14-3-3σ in podocytes was expressed in the primary processes. 14-3-3σ interacted with vimentin but not with the actin-associated proteins FKBP12 and synaptopodin. Gene silencing for 14-3-3σ altered the structure of vimentin fibers and process formation. 14-3-3σ and vimentin expression was increased in the early phase of podocyte injury models but was decreased in the late stage. Together, the localization of 14-3-3β at actin cytoskeleton plays a role in maintaining the foot processes and the Par complex in podocytes. In contrast, 14-3-3σ at vimentin cytoskeleton is essential for maintaining primary processes.
    MeSH term(s) Actins ; Podocytes ; 14-3-3 Proteins/genetics ; Tacrolimus Binding Protein 1A ; Vimentin/genetics ; Kidney
    Chemical Substances Actins ; 14-3-3 Proteins ; Tacrolimus Binding Protein 1A (EC 5.2.1.-) ; Vimentin
    Language English
    Publishing date 2022-09-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 639186-2
    ISSN 1530-6860 ; 0892-6638
    ISSN (online) 1530-6860
    ISSN 0892-6638
    DOI 10.1096/fj.202300865R
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  6. Article ; Online: New insight into podocyte slit diaphragm, a therapeutic target of proteinuria.

    Kawachi, Hiroshi / Fukusumi, Yoshiyasu

    Clinical and experimental nephrology

    2020  Volume 24, Issue 3, Page(s) 193–204

    Abstract: Dysfunction of slit diaphragm, a cell-cell junction of glomerular podocytes, is involved in the development of proteinuria in several glomerular diseases. Slit diaphragm should be a target of a novel therapy for proteinuria. Nephrin, NEPH1, P-cadherin, ... ...

    Abstract Dysfunction of slit diaphragm, a cell-cell junction of glomerular podocytes, is involved in the development of proteinuria in several glomerular diseases. Slit diaphragm should be a target of a novel therapy for proteinuria. Nephrin, NEPH1, P-cadherin, FAT, and ephrin-B1 were reported to be extracellular components forming a molecular sieve of the slit diaphragm. Several cytoplasmic proteins such as ZO-1, podocin, CD2AP, MAGI proteins and Par-complex molecules were identified as scaffold proteins linking the slit diaphragm to the cytoskeleton. In this article, new insights into these molecules and the pathogenic roles of the dysfunction of these molecules were introduced. The slit diaphragm functions not only as a barrier but also as a signaling platform transfer the signal to the inside of the cell. For maintaining the slit diaphragm function properly, the phosphorylation level of nephrin is strictly regulated. The recent studies on the signaling pathway from nephrin, NEPH1, and ephrin-B1 were reviewed. Although the mechanism regulating the function of the slit diaphragm had remained unclear, recent studies revealed TRPC6 and angiotensin II-regulating mechanisms play a critical role in regulating the barrier function of the slit diaphragm. In this review, recent investigations on the regulation of the slit diaphragm function were reviewed, and a strategy for the establishment of a novel therapy for proteinuria was proposed.
    MeSH term(s) Humans ; Intercellular Junctions ; Molecular Targeted Therapy ; Podocytes ; Proteinuria/therapy
    Language English
    Publishing date 2020-02-04
    Publishing country Japan
    Document type Journal Article ; Review
    ZDB-ID 1338768-6
    ISSN 1437-7799 ; 1342-1751
    ISSN (online) 1437-7799
    ISSN 1342-1751
    DOI 10.1007/s10157-020-01854-3
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  7. Article: PSmad3+/Olig2- expression defines a subpopulation of

    Ohyama, Kyoji / Shinohara, Hiroshi M / Omura, Shoichiro / Kawachi, Tomomi / Sato, Toru / Toda, Keiko

    Frontiers in neuroscience

    2023  Volume 17, Page(s) 1204012

    Abstract: In mouse dentate gyrus, radial glia-like cells (RGLs) persist throughout life and play a critical role in the generation of granule neurons. A large body of evidence has shown that the combinatorial expression of transcription factors (TFs) defines cell ... ...

    Abstract In mouse dentate gyrus, radial glia-like cells (RGLs) persist throughout life and play a critical role in the generation of granule neurons. A large body of evidence has shown that the combinatorial expression of transcription factors (TFs) defines cell types in the developing central nervous system (CNS). As yet, the identification of specific TFs that exclusively define RGLs in the developing mouse dentate gyrus (DG) remains elusive. Here we show that phospho-Smad3 (PSmad3) is expressed in a subpopulation of neural progenitors in the DG. During embryonic stage (E14-15), PSmad3 was predominantly expressed in
    Language English
    Publishing date 2023-09-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2411902-7
    ISSN 1662-453X ; 1662-4548
    ISSN (online) 1662-453X
    ISSN 1662-4548
    DOI 10.3389/fnins.2023.1204012
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  8. Article ; Online: Endoscopic three-categorical diagnosis of Helicobacter pylori infection using linked color imaging and deep learning: a single-center prospective study (with video).

    Nakashima, Hirotaka / Kawahira, Hiroshi / Kawachi, Hiroshi / Sakaki, Nobuhiro

    Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association

    2020  Volume 23, Issue 6, Page(s) 1033–1040

    Abstract: Background: Helicobacter pylori (H. pylori) eradication is required to reduce incidence related to gastric cancer. Recently, it was found that even after the successful eradication of H. pylori, an increased, i.e., moderate, risk of gastric cancer ... ...

    Abstract Background: Helicobacter pylori (H. pylori) eradication is required to reduce incidence related to gastric cancer. Recently, it was found that even after the successful eradication of H. pylori, an increased, i.e., moderate, risk of gastric cancer persists in patients with advanced mucosal atrophy and/or intestinal metaplasia. This study aimed to develop a computer-aided diagnosis (CAD) system to classify the status of H. pylori infection of patients into three categories: uninfected (with no history of H. pylori infection), currently infected, and post-eradication.
    Methods: The CAD system was based on linked color imaging (LCI) combined with deep learning (DL). First, a validation dataset was formed for the CAD systems by recording endoscopic movies of 120 subjects. Next, a training dataset of 395 subjects was prepared to enable DL. All endoscopic examinations were recorded using both LCI and white-light imaging (WLI). These endoscopic data were used to develop two different CAD systems, one for LCI (LCI-CAD) and one for WLI (WLI-CAD) images.
    Results: The diagnostic accuracy of the LCI-CAD system was 84.2% for uninfected, 82.5% for currently infected, and 79.2% for post-eradication status. Comparisons revealed superior accuracy of diagnoses based on LCI-CAD data relative based on WLI-CAD for uninfected, currently infected, and post-eradication cases. Furthermore, the LCI-CAD system demonstrated comparable diagnostic accuracy to that of experienced endoscopists with the validation data set of LCI.
    Conclusions: The results of this study suggest the feasibility of an innovative gastric cancer screening program to determine cancer risk in individual subjects based on LCI-CAD.
    MeSH term(s) Aged ; Area Under Curve ; Atrophy ; Color ; Deep Learning ; Diagnosis, Computer-Assisted/methods ; Endoscopy, Digestive System/methods ; Feasibility Studies ; Female ; Gastric Mucosa/diagnostic imaging ; Gastric Mucosa/pathology ; Helicobacter Infections/classification ; Helicobacter Infections/diagnosis ; Helicobacter pylori ; Humans ; Image Enhancement/methods ; Male ; Middle Aged ; Predictive Value of Tests ; Prospective Studies ; Sensitivity and Specificity
    Language English
    Publishing date 2020-05-07
    Publishing country Japan
    Document type Clinical Study ; Journal Article ; Video-Audio Media
    ZDB-ID 1463526-4
    ISSN 1436-3305 ; 1436-3291
    ISSN (online) 1436-3305
    ISSN 1436-3291
    DOI 10.1007/s10120-020-01077-1
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  9. Article ; Online: Nephrin-Ephrin-B1-Na

    Fukusumi, Yoshiyasu / Yasuda, Hidenori / Zhang, Ying / Kawachi, Hiroshi

    The American journal of pathology

    2021  Volume 191, Issue 7, Page(s) 1209–1226

    Abstract: Ephrin-B1 is one of the critical components of the slit diaphragm of kidney glomerular podocyte. However, the precise function of ephrin-B1 is unclear. To clarify the function of ephrin-B1, ephrin-B1-associated molecules were studied. RNA-sequencing ... ...

    Abstract Ephrin-B1 is one of the critical components of the slit diaphragm of kidney glomerular podocyte. However, the precise function of ephrin-B1 is unclear. To clarify the function of ephrin-B1, ephrin-B1-associated molecules were studied. RNA-sequencing analysis suggested that Na
    MeSH term(s) Animals ; Ephrin-B1/metabolism ; HEK293 Cells ; Humans ; Kidney Diseases/metabolism ; Kidney Diseases/pathology ; Membrane Proteins/metabolism ; Mice ; Mice, Knockout ; Phosphoproteins/metabolism ; Podocytes/metabolism ; Podocytes/pathology ; Rats ; Rats, Wistar ; Sodium-Hydrogen Exchangers/metabolism
    Chemical Substances Ephrin-B1 ; Membrane Proteins ; Phosphoproteins ; Sodium-Hydrogen Exchangers ; nephrin ; sodium-hydrogen exchanger regulatory factor
    Language English
    Publishing date 2021-04-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2943-9
    ISSN 1525-2191 ; 0002-9440
    ISSN (online) 1525-2191
    ISSN 0002-9440
    DOI 10.1016/j.ajpath.2021.04.004
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  10. Article ; Online: Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder.

    Hongo, Shoko / Shimizu, Hiroshi / Saji, Etsuji / Nakajima, Akihiro / Okamoto, Kouichirou / Kawachi, Izumi / Onodera, Osamu / Kakita, Akiyoshi

    Neuropathology : official journal of the Japanese Society of Neuropathology

    2024  

    Abstract: An 84-year-old man presented with somnolence, dysphagia, and right hemiplegia, all occurring within a month, approximately one year after initial admission due to subacute, transient cognitive decline suggestive of acute disseminated encephalomyelitis ... ...

    Abstract An 84-year-old man presented with somnolence, dysphagia, and right hemiplegia, all occurring within a month, approximately one year after initial admission due to subacute, transient cognitive decline suggestive of acute disseminated encephalomyelitis involving the cerebral white matter. Serial magnetic resonance imaging (MRI) studies over that period revealed three high-intensity signal lesions on fluid-attenuated inversion recovery images, appearing in chronological order in the left upper and left lower medulla oblongata and left pontine base. Despite some clinical improvement following methylprednisolone pulse therapy, the patient died of respiratory failure. Autopsy revealed four fresh, well-defined lesions in the brainstem, three of which corresponded to the lesions detected radiologically. The remaining lesion was located in the dorsal medulla oblongata and involved the right solitary nucleus. This might have appeared at a later disease stage, eventually causing respiratory failure. Histologically, all four lesions showed loss of myelin, preservation of axons, and infiltration of lymphocytes, predominantly CD8-positive T cells, consistent with the histological features of autoimmune demyelinating diseases, particularly the confluent demyelination observed in the early and acute phases of multiple sclerosis (MS). In the cerebral white matter, autoimmune demyelination appeared superimposed on ischemic changes, consistent with the cerebrospinal fluid (CSF) and MRI findings on initial admission. No anti-AQP4 or MOG antibodies or those potentially causing autoimmune encephalitis/demyelination were detected in either the serum or CSF. Despite several similarities to MS, such as the relapsing-remitting disease course and lesion histology, the entire clinicopathological picture in the present patient, especially the advanced age at onset and development of brainstem lesions in close proximity within a short time frame, did not fit those of MS or other autoimmune diseases that are currently established. The present results suggest that exceptionally older individuals can be affected by an as yet unknown inflammatory demyelinating disease of the CNS.
    Language English
    Publishing date 2024-04-07
    Publishing country Australia
    Document type Case Reports
    ZDB-ID 1483794-8
    ISSN 1440-1789 ; 0919-6544
    ISSN (online) 1440-1789
    ISSN 0919-6544
    DOI 10.1111/neup.12976
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