LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 3910

Search options

  1. Article ; Online: Fucoxanthin inhibits gastric cancer lymphangiogenesis and metastasis by regulating Ran expression.

    Wang, Jia / Dong, Xue / Li, Dandan / Fang, Zhiyao / Wan, Xianyao / Liu, Jing

    Phytomedicine : international journal of phytotherapy and phytopharmacology

    2023  Volume 118, Page(s) 154926

    Abstract: ... showed that Ran was highly expressed in metastatic lymph nodes and has some predictive value ... of Ran via hydrogen bonds. Mechanistically, fucoxanthin inhibits the nuclear transport of NF-κB ... by downregulating protein expression of Ran and importinβ, thereby inhibiting VEGF-C secretion, and ultimately ...

    Abstract Background: Lymph node metastasis is a key mechanism in gastric cancer (GC) metastasis and lymphangiogenesis is a vital step in the process of lymph node metastasis. Currently, there are no drugs which can treat lymph node metastasis in GC. Previous studies using the drug fucoxanthin have mainly focused on cell cycle arrest, induction of apoptosis, or inhibition of angiogenesis in GC. However, the effects of fucoxanthin on lymphangiogenesis and metastasis in GC have not been studied.
    Methods: Cell counting kit 8 and transwell experiments were used to evaluate the inhibitory effect of fucoxanthin on cell proliferation, migration and invasion. HGC-27 and HLEC cells were co-cultured in a transwell chamber and the footpad metastasis model was established to evaluate lymphangiogenesis and lymph node metastasis. The possible regulatory targets of fucoxanthin in GC were analyzed using human tissue microarrays, bioinformatics analysis, and molecular docking. The regulatory pathway of fucoxanthin was verified using confocal laser microscopy, adenovirus transfection and western blotting.
    Results: Tissue microarray and bioinformatics analyses showed that Ran was highly expressed in metastatic lymph nodes and has some predictive value for metastasis in GC. Molecular docking results revealed that fucoxanthin interacted with Met189 and Lys167 of Ran via hydrogen bonds. Mechanistically, fucoxanthin inhibits the nuclear transport of NF-κB by downregulating protein expression of Ran and importinβ, thereby inhibiting VEGF-C secretion, and ultimately inhibiting tumor lymphangiogenesis and lymph node metastasis in vivo and in vitro.
    Conclusions: Fucoxanthin suppressed GC-induced lymphangiogenesis and metastasis in vitro and in vivo by regulating Ran expression via the importinβ/NF-κB/VEGF-C nuclear transport signaling pathway. These novel findings provide the basis for the research and development of novel treatments using traditional Chinese medicine in treatment of lymph node metastasis, which has important theoretical significance and clinical value.
    MeSH term(s) Humans ; Lymphangiogenesis ; Lymphatic Metastasis ; NF-kappa B/metabolism ; Vascular Endothelial Growth Factor C/metabolism ; Stomach Neoplasms/drug therapy ; Molecular Docking Simulation ; Cell Line, Tumor
    Chemical Substances NF-kappa B ; Vascular Endothelial Growth Factor C ; fucoxanthin (06O0TC0VSM)
    Language English
    Publishing date 2023-06-16
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1205240-1
    ISSN 1618-095X ; 0944-7113
    ISSN (online) 1618-095X
    ISSN 0944-7113
    DOI 10.1016/j.phymed.2023.154926
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Effects of Ran-GTP/importin β inhibition on the meiotic division of porcine oocytes.

    He, Yijing / Li, Jia / Peng, Lei / Li, Qiao / Chu, Yajie / Lin, Qixin / Dai, Jianjun / Rui, Rong / Ju, Shiqiang

    Histochemistry and cell biology

    2022  Volume 158, Issue 6, Page(s) 571–582

    Abstract: The Ran-GTP/importin β pathway has been implicated in a diverse array of mitotic functions ... in somatic mitosis; however, the possible meiotic roles of Ran-GTP/importin β in mammalian oocyte meiosis are ... of the interaction between Ran and importin β was used to explore the potential meiotic roles of Ran-GTP/importin β ...

    Abstract The Ran-GTP/importin β pathway has been implicated in a diverse array of mitotic functions in somatic mitosis; however, the possible meiotic roles of Ran-GTP/importin β in mammalian oocyte meiosis are still not fully understood. In the present study, importazole (IPZ), a small molecule inhibitor of the interaction between Ran and importin β was used to explore the potential meiotic roles of Ran-GTP/importin β in porcine oocytes undergoing meiosis. After IPZ treatment, the extrusion rate of the first polar body (PB1) was significantly decreased, and a higher proportion of the oocytes were arrested at the germinal vesicle breakdown (GVBD) stage. Moreover, IPZ treatment led to severe defects in metaphase I (MI) spindle assembly and chromosome alignment during the germinal vesicle (GV)-to-MI stage, as well as failure of metaphase II (MII) spindle reassembly and homologous chromosome segregation during the MI-to-MII stage. Notably, IPZ treatment decreased TPX2 expression and abnormal subcellular localization. Furthermore, the expression levels of aurora kinase A (AURKA) and transforming acidic coiled-coil 3 (TACC3) were significantly reduced after IPZ treatment. Collectively, these data indicate that the interaction of Ran-GTP and importin β is essential for proper spindle assembly and successful chromosome segregation during two consecutive meiotic divisions in porcine oocytes, and regulation of this complex might be related to its effect on the TPX2 signaling cascades.
    MeSH term(s) Swine ; Animals ; beta Karyopherins ; Quinazolines ; Signal Transduction ; Guanosine Triphosphate ; Mammals
    Chemical Substances beta Karyopherins ; Quinazolines ; Guanosine Triphosphate (86-01-1)
    Language English
    Publishing date 2022-08-05
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1222930-1
    ISSN 1432-119X ; 0301-5564 ; 0948-6143
    ISSN (online) 1432-119X
    ISSN 0301-5564 ; 0948-6143
    DOI 10.1007/s00418-022-02134-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Hyodeoxycholic acid ameliorates nonalcoholic fatty liver disease by inhibiting RAN-mediated PPARα nucleus-cytoplasm shuttling.

    Zhong, Jing / He, Xiaofang / Gao, Xinxin / Liu, Qiaohong / Zhao, Yu / Hong, Ying / Zhu, Weize / Yan, Juan / Li, Yifan / Li, Yan / Zheng, Ningning / Bao, Yiyang / Wang, Hao / Ma, Junli / Huang, Wenjin / Liu, Zekun / Lyu, Yuanzhi / Ke, Xisong / Jia, Wei /
    Xie, Cen / Hu, Yiyang / Sheng, Lili / Li, Houkai

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 5451

    Abstract: ... HDCA facilitates nuclear localization of PPARα by directly interacting with RAN ... protein. This interaction disrupts the formation of RAN/CRM1/PPARα nucleus-cytoplasm shuttling heterotrimer. Our results ...

    Abstract Nonalcoholic fatty liver disease (NAFLD) is usually characterized with disrupted bile acid (BA) homeostasis. However, the exact role of certain BA in NAFLD is poorly understood. Here we show levels of serum hyodeoxycholic acid (HDCA) decrease in both NAFLD patients and mice, as well as in liver and intestinal contents of NAFLD mice compared to their healthy counterparts. Serum HDCA is also inversely correlated with NAFLD severity. Dietary HDCA supplementation ameliorates diet-induced NAFLD in male wild type mice by activating fatty acid oxidation in hepatic peroxisome proliferator-activated receptor α (PPARα)-dependent way because the anti-NAFLD effect of HDCA is abolished in hepatocyte-specific Pparα knockout mice. Mechanistically, HDCA facilitates nuclear localization of PPARα by directly interacting with RAN protein. This interaction disrupts the formation of RAN/CRM1/PPARα nucleus-cytoplasm shuttling heterotrimer. Our results demonstrate the therapeutic potential of HDCA for NAFLD and provide new insights of BAs on regulating fatty acid metabolism.
    MeSH term(s) Male ; Animals ; Mice ; Non-alcoholic Fatty Liver Disease/drug therapy ; PPAR alpha/genetics ; Bile Acids and Salts ; Cytoplasm ; Mice, Knockout ; Fatty Acids
    Chemical Substances PPAR alpha ; hyodeoxycholic acid (7A33Y6EHYK) ; Bile Acids and Salts ; Fatty Acids
    Language English
    Publishing date 2023-09-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-41061-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Design and structural characterization of autoinhibition-compromised full-length Ran.

    Tan, Yuping / Zhang, Yuqing / Zhou, Qiao / Jia, Da / Sun, Qingxiang

    Signal transduction and targeted therapy

    2021  Volume 6, Issue 1, Page(s) 44

    MeSH term(s) Amino Acid Sequence/genetics ; Crystallography, X-Ray ; Escherichia coli/genetics ; Evolution, Molecular ; Humans ; Mutation/genetics ; Protein Conformation ; Saccharomyces cerevisiae/genetics ; Sequence Alignment ; ran GTP-Binding Protein/chemistry ; ran GTP-Binding Protein/genetics ; ran GTP-Binding Protein/ultrastructure
    Chemical Substances ran GTP-Binding Protein (EC 3.6.5.2)
    Language English
    Publishing date 2021-02-03
    Publishing country England
    Document type Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 2886872-9
    ISSN 2059-3635 ; 2095-9907
    ISSN (online) 2059-3635
    ISSN 2095-9907
    DOI 10.1038/s41392-020-00398-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Design and structural characterization of autoinhibition-compromised full-length Ran

    Yuping Tan / Yuqing Zhang / Qiao Zhou / Da Jia / Qingxiang Sun

    Signal Transduction and Targeted Therapy, Vol 6, Iss 1, Pp 1-

    2021  Volume 3

    Keywords Medicine ; R ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2021-02-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  6. Article ; Online: RAN and YBX1 are required for cell proliferation and IL-4 expression and linked to poor prognosis in oral squamous cell carcinoma.

    Che, Xiaoxuan / Liu, Miaomiao / Li, Di / Li, Ziwei / Guo, Jihua / Jia, Rong

    Experimental cell research

    2021  Volume 406, Issue 2, Page(s) 112767

    Abstract: ... with a high mortality rate. RAN is a member of the Ras GTPase family and is overexpressed in a range ... of cancers, however, the relationship between RAN and OSCC is rarely reported. In this study, we found ... that RAN is overexpressed in OSCC tissues. RAN inhibition retarded OSCC cell proliferation and led ...

    Abstract Oral squamous cell carcinoma (OSCC) is one of the most common malignancies in the world, with a high mortality rate. RAN is a member of the Ras GTPase family and is overexpressed in a range of cancers, however, the relationship between RAN and OSCC is rarely reported. In this study, we found that RAN is overexpressed in OSCC tissues. RAN inhibition retarded OSCC cell proliferation and led to apoptosis and cell cycle arrest. Knockdown of RAN inhibited tumor growth in vivo. Strikingly, we found that RAN and oncogene Y-box binding protein-1 (YBX1) are positively associated with the immune infiltrates of CD4
    MeSH term(s) Animals ; Apoptosis ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Carcinoma, Squamous Cell/genetics ; Carcinoma, Squamous Cell/metabolism ; Carcinoma, Squamous Cell/pathology ; Cell Cycle ; Cell Movement ; Cell Proliferation ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Interleukin-4/genetics ; Interleukin-4/metabolism ; Male ; Mice ; Mice, Nude ; Middle Aged ; Mouth Neoplasms/metabolism ; Mouth Neoplasms/pathology ; Prognosis ; Retrospective Studies ; Survival Rate ; Tumor Cells, Cultured ; Xenograft Model Antitumor Assays ; Y-Box-Binding Protein 1/genetics ; Y-Box-Binding Protein 1/metabolism ; ran GTP-Binding Protein/genetics ; ran GTP-Binding Protein/metabolism
    Chemical Substances Biomarkers, Tumor ; IL4 protein, human ; RAN protein, human ; Y-Box-Binding Protein 1 ; YBX1 protein, human ; Interleukin-4 (207137-56-2) ; ran GTP-Binding Protein (EC 3.6.5.2)
    Language English
    Publishing date 2021-08-05
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1493-x
    ISSN 1090-2422 ; 0014-4827
    ISSN (online) 1090-2422
    ISSN 0014-4827
    DOI 10.1016/j.yexcr.2021.112767
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: GEF-independent Ran activation shifts a fraction of the protein to the cytoplasm and promotes cell proliferation.

    Zhou, Jinhan / Tan, Yuping / Zhang, Yuqing / Tong, Aiping / Shen, Xiaofei / Sun, Xiaodong / Jia, Da / Sun, Qingxiang

    Molecular biomedicine

    2020  Volume 1, Issue 1, Page(s) 18

    Abstract: Ran (Ras-related nuclear protein) plays several important roles in nucleo-cytoplasmic transport ... superfamily, Ran binds more tightly to GDP than to GTP due to the presence of an auto-inhibitory C-terminal ... tail. Multiple missense mutations in the C-terminus of Ran occur in cancers, but their biological ...

    Abstract Ran (Ras-related nuclear protein) plays several important roles in nucleo-cytoplasmic transport, mitotic spindle formation, nuclear envelope/nuclear pore complex assembly, and other functions in the cytoplasm, as well as in cellular transformation when switched on. Unlike other members of the GTPase superfamily, Ran binds more tightly to GDP than to GTP due to the presence of an auto-inhibitory C-terminal tail. Multiple missense mutations in the C-terminus of Ran occur in cancers, but their biological significance remains unclear. Here, the quantitative GDP/GTP binding preference of four engineered mutations with unstable C-termini was analyzed using a devised mant-GDP dissociation assay. The results showed that the impact of different C-terminal mutations depends on multiple factors. Although these mutants were more GTP-loaded in human cells, they were shown to be more cytoplasmic, and to support nuclear transport with minimally or partially reduced efficiency. Further, several Ran cancer mutants were compromised in autoinhibition, slightly more GTP-bound, more cytoplasmic, and enhanced the proliferation of A549 and HeLa cells in vitro. Thus, our work reveals a new route of Ran activation independent of guanine nucleotide exchange factor (GEF), which may account for the hyper-proliferation induced by Ran cancer mutations.
    Language English
    Publishing date 2020-12-30
    Publishing country Singapore
    Document type Journal Article
    ISSN 2662-8651
    ISSN (online) 2662-8651
    DOI 10.1186/s43556-020-00011-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: Ran-binding protein M is associated with human spermatogenesis and oogenesis.

    Tang, Wen-Hao / Zhuang, Xin-Jie / Song, Shi-De / Wu, Han / Zhang, Zhe / Yang, Yu-Zhuo / Zhang, Hong-Liang / Mao, Jia-Ming / Liu, De-Feng / Zhao, Lian-Ming / Lin, Hao-Cheng / Hong, Kai / Ma, Lu-Lin / Qiao, Jie / Qin, Weibing / Tang, Yunge / Jiang, Hui

    Molecular medicine reports

    2018  Volume 17, Issue 2, Page(s) 2257–2262

    Abstract: ... of Ran‑binding protein M (RanBPM) in human spermatogenesis and oogenesis. RanBPM expression in human ...

    Abstract The aim of the present study was to explore the underlying mechanism and diagnostic potential of Ran‑binding protein M (RanBPM) in human spermatogenesis and oogenesis. RanBPM expression in human testis and ovaries was analysed using polymerase chain reaction (PCR) and western blotting, and immunofluorescence was performed on testis and ovary tissue sections during different developmental stages of spermatogenesis and oogenesis using RanBPM antibodies. Interactions with a variety of functional proteins were also investigated. RanBPM mRNA and protein expression levels were determined by PCR and western blotting in the tissue sections. Results revealed that the mRNA expression levels were highest in the testis followed by the ovary. The RanBPM protein was predominantly localized in the nucleus of germ cells, and the expression levels were highest in pachytene spermatocytes and cells surrounding spermatids in testis tissue. In ovary cells, RanBPM was localized in the nucleus and cytoplasm. In conclusion, the results suggested that RanBPM may have multiple roles in the regulation of germ cell proliferation during human spermatogenesis and oogenesis. This research may provide a novel insight into the underlying molecular mechanism of RanBPM and may have implications for the clinical diagnosis and treatment of human infertility.
    MeSH term(s) Adaptor Proteins, Signal Transducing/chemistry ; Adaptor Proteins, Signal Transducing/genetics ; Adaptor Proteins, Signal Transducing/metabolism ; Adult ; Amino Acid Sequence ; Cytoskeletal Proteins/chemistry ; Cytoskeletal Proteins/genetics ; Cytoskeletal Proteins/metabolism ; Female ; Gene Expression ; Humans ; Immunohistochemistry ; Male ; Nuclear Proteins/chemistry ; Nuclear Proteins/genetics ; Nuclear Proteins/metabolism ; Oogenesis/genetics ; Ovary/metabolism ; Spermatogenesis/genetics ; Testis/metabolism
    Chemical Substances Adaptor Proteins, Signal Transducing ; Cytoskeletal Proteins ; Nuclear Proteins ; Ran binding protein 9
    Language English
    Publishing date 2018-02
    Publishing country Greece
    Document type Journal Article
    ISSN 1791-3004
    ISSN (online) 1791-3004
    DOI 10.3892/mmr.2017.8147
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Corrigendum to: "Erythropoietin Preconditioning Mobilizes Endothelial Progenitor Cells to Attenuate Nephron-Sparing Surgery-Induced Ischemia-Reperfusion Injury" by Yunpeng Zhu, Kai Zhao, Longxin Wang, Tianze Lu, Changcheng Zhou, Yuzheng Ge, Ran Wu, Ruipeng Jia and Chuanqi Zheng, Transplantation Proceedings 2020;52/10: 2955-2963.

    Zhu, Yunpeng / Zhao, Kai / Lu, Tianze / Wang, Longxin / Zhou, Changcheng / Ge, Yuzheng / Wu, Ran / Jia, Ruipeng / Zheng, Qichuan

    Transplantation proceedings

    2021  Volume 55, Issue 7, Page(s) 1763

    Language English
    Publishing date 2021-10-09
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2021.09.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: GEF-independent Ran activation shifts a fraction of the protein to the cytoplasm and promotes cell proliferation

    Jinhan Zhou / Yuping Tan / Yuqing Zhang / Aiping Tong / Xiaofei Shen / Xiaodong Sun / Da Jia / Qingxiang Sun

    Molecular Biomedicine, Vol 1, Iss 1, Pp 1-

    2020  Volume 13

    Abstract: Abstract Ran (Ras-related nuclear protein) plays several important roles ... superfamily, Ran binds more tightly to GDP than to GTP due to the presence of an auto-inhibitory C-terminal ... tail. Multiple missense mutations in the C-terminus of Ran occur in cancers, but their biological ...

    Abstract Abstract Ran (Ras-related nuclear protein) plays several important roles in nucleo-cytoplasmic transport, mitotic spindle formation, nuclear envelope/nuclear pore complex assembly, and other functions in the cytoplasm, as well as in cellular transformation when switched on. Unlike other members of the GTPase superfamily, Ran binds more tightly to GDP than to GTP due to the presence of an auto-inhibitory C-terminal tail. Multiple missense mutations in the C-terminus of Ran occur in cancers, but their biological significance remains unclear. Here, the quantitative GDP/GTP binding preference of four engineered mutations with unstable C-termini was analyzed using a devised mant-GDP dissociation assay. The results showed that the impact of different C-terminal mutations depends on multiple factors. Although these mutants were more GTP-loaded in human cells, they were shown to be more cytoplasmic, and to support nuclear transport with minimally or partially reduced efficiency. Further, several Ran cancer mutants were compromised in autoinhibition, slightly more GTP-bound, more cytoplasmic, and enhanced the proliferation of A549 and HeLa cells in vitro. Thus, our work reveals a new route of Ran activation independent of guanine nucleotide exchange factor (GEF), which may account for the hyper-proliferation induced by Ran cancer mutations.
    Keywords Small GTPases ; Nuclear transport ; GTP bias ; Activation ; Cancer mutations ; Medicine ; R
    Subject code 570
    Language English
    Publishing date 2020-12-01T00:00:00Z
    Publisher Springer
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top