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  1. Article ; Online: Precursory or early lesions of follicular lymphoma: clinical features, pathology, and genetics.

    Oishi, Naoki

    Journal of clinical and experimental hematopathology : JCEH

    2023  Volume 63, Issue 2, Page(s) 65–72

    Abstract: Follicular lymphoma (FL) is an indolent B-cell lymphoma with a germinal center (GC) B cell phenotype that typically harbors t(14;18)(q32;q21). t(14;18) juxtaposes IGH on 14q32 and BCL2 on 18q21, resulting in overexpression of the anti-apoptotic BCL2 ... ...

    Abstract Follicular lymphoma (FL) is an indolent B-cell lymphoma with a germinal center (GC) B cell phenotype that typically harbors t(14;18)(q32;q21). t(14;18) juxtaposes IGH on 14q32 and BCL2 on 18q21, resulting in overexpression of the anti-apoptotic BCL2 protein. However, t(14;18) is also found in the peripheral blood or lymphoid nodes (LNs) of otherwise healthy individuals. Moreover, overt FL has several additional gene alterations involved in epigenetic modification, JAK/STAT signaling, immune modulation, and NF-κB signaling, indicating multi-step lymphomagenesis in FL. There are two early or precursory lesions of FL: t(14;18)-positive cells in the peripheral blood of otherwise healthy individuals and in situ follicular B-cell neoplasm (ISFN). t(14;18)-positive cells are found in 10%-50% of healthy populations, and their incidence and frequency increase with age. The detection of t(14;18) in peripheral blood is a predictive factor for an increased risk of overt FL development. In contrast, ISFN is a histopathologically recognizable precursory lesion, in which t(14;18)-positive cells are confined to the GC of otherwise reactive LNs. ISFN is usually detected incidentally, with an incidence ranging from 2.0% to 3.2%. Occasional ISFN cases have concurrent or metachronous clonally related overt FL or aggressive B-cell lymphoma of a GC phenotype. t(14;18)-positive cells in peripheral blood and isolated ISFN, by themselves, are asymptomatic with limited clinical significance; however, investigations of t(14;18)-positive precursory or early lesions offer meaningful insights into the pathogenesis of FL. This review summarizes the epidemiology, clinical features, pathology, and genetics of precursory or early lesions of FL.
    MeSH term(s) Humans ; Lymphoma, Follicular/diagnosis ; Lymphoma, Follicular/genetics ; B-Lymphocytes ; Lymph Nodes ; Lymphoma, B-Cell ; Proto-Oncogene Proteins c-bcl-2
    Chemical Substances Proto-Oncogene Proteins c-bcl-2
    Language English
    Publishing date 2023-06-26
    Publishing country Japan
    Document type Review ; Journal Article
    ZDB-ID 2395568-5
    ISSN 1880-9952 ; 1880-9952
    ISSN (online) 1880-9952
    ISSN 1880-9952
    DOI 10.3960/jslrt.23010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Current Concepts in Nodal Peripheral T-Cell Lymphomas.

    Oishi, Naoki / Feldman, Andrew L

    Surgical pathology clinics

    2023  Volume 16, Issue 2, Page(s) 267–285

    Abstract: This review summarizes the current understanding of mature T-cell neoplasms predominantly involving lymph nodes, including ALK-positive and ALK-negative anaplastic large cell lymphomas, nodal T-follicular helper cell lymphoma, Epstein-Barr virus-positive ...

    Abstract This review summarizes the current understanding of mature T-cell neoplasms predominantly involving lymph nodes, including ALK-positive and ALK-negative anaplastic large cell lymphomas, nodal T-follicular helper cell lymphoma, Epstein-Barr virus-positive nodal T/NK-cell lymphoma, and peripheral T-cell lymphoma (PTCL), not otherwise specified. These PTCLs are clinically, pathologically, and genetically heterogeneous, and the diagnosis is made by a combination of clinical information, morphology, immunophenotype, viral positivity, and genetic abnormalities. This review summarizes the pathologic features of common nodal PTCLs, highlighting updates in the fifth edition of the World Health Organization classification and the 2022 International Consensus Classification.
    MeSH term(s) Humans ; Lymphoma, T-Cell, Peripheral/diagnosis ; Lymphoma, T-Cell, Peripheral/genetics ; Lymphoma, T-Cell, Peripheral/pathology ; Epstein-Barr Virus Infections/diagnosis ; Epstein-Barr Virus Infections/pathology ; Herpesvirus 4, Human/genetics ; Lymph Nodes/pathology ; Receptor Protein-Tyrosine Kinases
    Chemical Substances Receptor Protein-Tyrosine Kinases (EC 2.7.10.1)
    Language English
    Publishing date 2023-04-03
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 1875-9157
    ISSN (online) 1875-9157
    DOI 10.1016/j.path.2023.01.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: CA9 expression in breast implant-associated anaplastic large cell lymphoma presenting in a lymph node.

    Oishi, Naoki / Feldman, Andrew L

    Histopathology

    2022  Volume 81, Issue 2, Page(s) 270–272

    MeSH term(s) Antigens, Neoplasm ; Breast Implants/adverse effects ; Breast Neoplasms/etiology ; Breast Neoplasms/pathology ; Carbonic Anhydrase IX ; Female ; Humans ; Lymph Nodes/pathology ; Lymphoma, Large-Cell, Anaplastic/etiology ; Lymphoma, Large-Cell, Anaplastic/pathology
    Chemical Substances Antigens, Neoplasm ; CA9 protein, human (EC 4.2.1.1) ; Carbonic Anhydrase IX (EC 4.2.1.1)
    Language English
    Publishing date 2022-04-27
    Publishing country England
    Document type Letter
    ZDB-ID 131914-0
    ISSN 1365-2559 ; 0309-0167
    ISSN (online) 1365-2559
    ISSN 0309-0167
    DOI 10.1111/his.14666
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Immunohistochemical detection of cancer genetic abnormalities.

    Le, Minh-Khang / Oishi, Naoki / Mochizuki, Kunio / Kondo, Tetsuo

    Pathology, research and practice

    2024  Volume 255, Page(s) 155109

    Abstract: New applications of immunohistochemistry (IHC) expand rapidly due to the development of molecular analyses and an increased understanding of molecular biology. IHC becomes much more important as a screening or even a confirmatory test for molecular ... ...

    Abstract New applications of immunohistochemistry (IHC) expand rapidly due to the development of molecular analyses and an increased understanding of molecular biology. IHC becomes much more important as a screening or even a confirmatory test for molecular changes in cancer. The past decades have witnessed the release of many immunohistochemical markers of the new generation. The novel markers have extensively high specificity and sensitivity for the detection of genetic abnormalities. In addition to diagnostic utility, IHC has been validated to be a practical tool in terms of treatments, especially molecular targeted therapy. In this review, we first describe the common alterations of protein IHC staining in human cancer: overexpression, underexpression, or loss of expression and altered staining pattern. Next, we examine the relationship between staining patterns and genetic aberrations regarding both conventional and novel IHC markers. We also mention current mutant-specific and fusion-specific antibodies and their concordance with molecular techniques. We then describe the basic molecular mechanisms from genetic events to corresponding protein expression patterns (membranous, cytoplasmic, or nuclear patterns). Finally, we shortly discuss the applications of immunohistochemistry in molecular targeted therapy. IHC markers can serve as a complementary or companion diagnostic test to provide valuable information for targeted therapy. Moreover, immunohistochemistry is also crucial as a companion diagnostic test in immunotherapy. The increased number of IHC novel antibodies is broadening its application in anti-cancer therapies.
    MeSH term(s) Humans ; Neoplasms/diagnosis ; Neoplasms/genetics ; Immunohistochemistry ; Antibodies
    Chemical Substances Antibodies
    Language English
    Publishing date 2024-02-01
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 391889-0
    ISSN 1618-0631 ; 0344-0338
    ISSN (online) 1618-0631
    ISSN 0344-0338
    DOI 10.1016/j.prp.2024.155109
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Expression of TGF-β1 in Gastrointestinal Stromal Tumor (GIST) and the Occurrence of Frequent Desmoplasia.

    Mochizuki, Kunio / Oishi, Naoki / Tahara, Ippei / Inoue, Tomohiro / Kondo, Tetsuo

    Applied immunohistochemistry & molecular morphology : AIMM

    2024  

    Abstract: Gastrointestinal stromal tumors (GISTs) are mesenchymal neoplasms with variable behavior characterized by differentiation toward the interstitial cells of Cajal occurring anywhere in the gastrointestinal stromal tract. Frequently, GISTs have fibrous ... ...

    Abstract Gastrointestinal stromal tumors (GISTs) are mesenchymal neoplasms with variable behavior characterized by differentiation toward the interstitial cells of Cajal occurring anywhere in the gastrointestinal stromal tract. Frequently, GISTs have fibrous stroma within tumor cell proliferation areas, which is unlike other types of malignant tumors. If this desmoplasia is active, there is a possibility that some sort of transmitter exists between GIST cells and cells related to fibrosis in the tumor cell proliferation areas. Transforming growth factor (TGF)-β isoforms, particularly TGF-β1, are critical for fibrosis pathogenesis. TGF-β1 regulation of myofibroblasts and fibroblasts during fibrosis is well described. The induced fibroblast activation resulting in myofibroblast differentiation has been reported as an important source of collagen, glycoproteins, proteoglycans, and matrix metallopeptidases in wound healing and fibrosis. However, there are a few reports on the relationship between TGF-β1 and GISTs. This study aims to clarify TGF-β1 expression in 30 gastric GISTs using immunohistochemistry and reverse transcription polymerase chain reaction (RT-PCR). For comparison, we also enrolled 30 samples of gastric tubular adenocarcinoma (GTAC). We confirmed TGF-β1 expression (H-score ≥50 points) in 57% of GIST and 13% of GTAC samples, a significant difference between the 2 tumor types (P=0.001). We examined the TGF-β1 mRNA expression of 3 representative GIST samples, each having their respective immunostained areas detected by RT-PCR. Finding TGF-β1 expression may indicate that this cytokine plays a part in the formation of desmoplasia within GIST cell proliferative areas.
    Language English
    Publishing date 2024-04-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1473273-7
    ISSN 1533-4058 ; 1062-3345 ; 1541-2016
    ISSN (online) 1533-4058
    ISSN 1062-3345 ; 1541-2016
    DOI 10.1097/PAI.0000000000001196
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Facial nerve schwannoma and other benign neoplastic facial nerve lesions.

    Kitama, Tsubasa / Hosoya, Makoto / Oishi, Naoki

    Current opinion in otolaryngology & head and neck surgery

    2023  Volume 31, Issue 5, Page(s) 300–305

    Abstract: Purpose of review: Several neoplastic lesions may originate from facial nerves, including facial nerve schwannomas. These neoplastic lesions can cause various symptoms, such as facial nerve paralysis, and decrease the quality of life of patients. ... ...

    Abstract Purpose of review: Several neoplastic lesions may originate from facial nerves, including facial nerve schwannomas. These neoplastic lesions can cause various symptoms, such as facial nerve paralysis, and decrease the quality of life of patients. Therefore, knowledge of how to manage these diseases is important for otologists. However, the incidence of these diseases is extremely low, and universal management methods have not yet been established. This review summarizes recent advances in knowledge regarding these neoplastic lesions, especially facial nerve schwannomas.
    Recent findings: Recent advances and the accumulation of knowledge regarding these benign facial nerve lesions have provided several preferable treatments and management methods, especially for facial nerve schwannomas. However, this still depends on the patient's symptoms and tumor localization.
    Summary: This review presents the optimal treatment protocol and differential diagnosis of benign facial nerve lesions. This may be useful for pretreatment differentiation and treatment decision-making.
    MeSH term(s) Humans ; Facial Nerve ; Quality of Life ; Neurilemmoma/diagnosis ; Neurilemmoma/complications ; Neurilemmoma/pathology ; Cranial Nerve Neoplasms/diagnosis ; Cranial Nerve Neoplasms/surgery ; Cranial Nerve Neoplasms/complications ; Facial Paralysis/etiology
    Language English
    Publishing date 2023-07-19
    Publishing country United States
    Document type Review ; Journal Article
    ZDB-ID 1232518-1
    ISSN 1531-6998 ; 1068-9508
    ISSN (online) 1531-6998
    ISSN 1068-9508
    DOI 10.1097/MOO.0000000000000913
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: A traction device to aid the intubation of a surgically altered bile duct during ERCP.

    Suda, Tsuyoshi / Yanagi, Masahiro / Oishi, Naoki / Matsushita, Eiki

    Endoscopy

    2022  Volume 54, Issue S 02, Page(s) E900–E901

    Language English
    Publishing date 2022-07-01
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 80120-3
    ISSN 1438-8812 ; 0013-726X
    ISSN (online) 1438-8812
    ISSN 0013-726X
    DOI 10.1055/a-1847-7609
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Synthesis of labionin and avionin precursors

    Yamaguchi, Ayuta / Obiya, Naoki / Arichi, Norihito / Oishi, Shinya / Ohno, Hiroaki / Inuki, Shinsuke

    Organic & biomolecular chemistry

    2024  Volume 22, Issue 10, Page(s) 2049–2055

    Abstract: Labionin and avionin are non-proteinogenic amino acids containing 2,4-diamino-2-(mercaptomethyl)pentanedioic acid that forms the core structures of spirocyclic peptides including labyrinthopeptin A2 and microvionin, respectively. We have developed a ... ...

    Abstract Labionin and avionin are non-proteinogenic amino acids containing 2,4-diamino-2-(mercaptomethyl)pentanedioic acid that forms the core structures of spirocyclic peptides including labyrinthopeptin A2 and microvionin, respectively. We have developed a diastereoselective synthetic route to labionin and avionin precursors. This route highlights the formation of the quaternary carbon stereocenter of an α,α-disubstituted amino acid
    Language English
    Publishing date 2024-03-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 2097583-1
    ISSN 1477-0539 ; 1477-0520
    ISSN (online) 1477-0539
    ISSN 1477-0520
    DOI 10.1039/d3ob02037a
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Updates in the Classification of T-cell Lymphomas and Lymphoproliferative Disorders.

    Oishi, Naoki / Ahmed, Reham / Feldman, Andrew L

    Current hematologic malignancy reports

    2023  Volume 18, Issue 6, Page(s) 252–263

    Abstract: Purpose of review: Mature T/NK-cell neoplasms comprise a heterogeneous group of diseases with diverse clinical, histopathologic, immunophenotypic, and molecular features. A clinically relevant, comprehensive, and reproducible classification system for T/ ...

    Abstract Purpose of review: Mature T/NK-cell neoplasms comprise a heterogeneous group of diseases with diverse clinical, histopathologic, immunophenotypic, and molecular features. A clinically relevant, comprehensive, and reproducible classification system for T/NK-cell neoplasms is essential for optimal management, risk stratification, and advancing understanding of these diseases. Two classification systems for lymphoid neoplasms were recently introduced: the 5th edition of World Health Organization classification (WHO-HAEM5) and the 2022 International Consensus Classification (ICC). In this review, we summarize the basic framework and updates in the classification of mature T/NK-cell neoplasms.
    Recent findings: WHO-HAEM5 and ICC share basic concepts in classification of T/NK-cell neoplasms, emphasizing integration of clinical presentation, pathology, immunophenotype, and genetics. Major updates in both classifications include unifying nodal T-follicular helper-cell lymphomas into a single entity and establishing EBV-positive nodal T/NK-cell lymphoma as a distinct entity. However, some differences exist in taxonomy, terminology, and disease definitions. The recent classifications of mature T/NK-cell neoplasms are largely similar and provide new insights into taxonomy based on integrated clinicopathologic features.
    MeSH term(s) Humans ; Lymphoma, T-Cell/diagnosis ; Lymphoma, T-Cell/pathology ; Lymphoproliferative Disorders/diagnosis ; Lymphoproliferative Disorders/pathology ; Lymphoma/pathology ; Killer Cells, Natural
    Language English
    Publishing date 2023-10-23
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2229765-0
    ISSN 1558-822X ; 1558-8211
    ISSN (online) 1558-822X
    ISSN 1558-8211
    DOI 10.1007/s11899-023-00712-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: [No title information]

    Seike, Takuya / Kanaya, Taro / Oishi, Naoki

    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne

    2022  Volume 194, Issue 26, Page(s) E936–E937

    Title translation Syndrome de choc toxique menstruel.
    MeSH term(s) Humans ; Menstrual Hygiene Products ; Shock, Septic ; Staphylococcal Infections
    Language French
    Publishing date 2022-08-02
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 215506-0
    ISSN 1488-2329 ; 0008-4409 ; 0820-3946
    ISSN (online) 1488-2329
    ISSN 0008-4409 ; 0820-3946
    DOI 10.1503/cmaj.211284-f
    Database MEDical Literature Analysis and Retrieval System OnLINE

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