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  1. AU="Han, Chenguang"
  2. AU="Ayoub, Isabelle"
  3. AU="Spencer, Sean P"
  4. AU="Papathemelis, Thomas"
  5. AU="Tzerefos, Christos"
  6. AU="Eefje Belt-van Zoen"
  7. AU="Rahmanian, Vahid"
  8. AU="Øyen, Martin Øhlund"
  9. AU="Xinyun Xuan"
  10. AU="Dana L. M. Campbell"
  11. AU="Mukta Roy"
  12. AU="Martha Funabashi"
  13. AU="Vasina, Svetlana"
  14. AU=Reber Stephan A.
  15. AU="Kenan Onel"
  16. AU="Lawrence, Marc R"
  17. AU="Zeiler, Frederick A"
  18. AU="de la Cueva, Pablo"
  19. AU="Fuh, Jerry Ying Hsi"
  20. AU="Park, Adrian J"
  21. AU="Joshi, K D"

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  1. Artikel ; Online: MGCNSS: miRNA-disease association prediction with multi-layer graph convolution and distance-based negative sample selection strategy.

    Tian, Zhen / Han, Chenguang / Xu, Lewen / Teng, Zhixia / Song, Wei

    Briefings in bioinformatics

    2024  Band 25, Heft 3

    Abstract: Identifying disease-associated microRNAs (miRNAs) could help understand the deep mechanism of diseases, which promotes the development of new medicine. Recently, network-based approaches have been widely proposed for inferring the potential associations ... ...

    Abstract Identifying disease-associated microRNAs (miRNAs) could help understand the deep mechanism of diseases, which promotes the development of new medicine. Recently, network-based approaches have been widely proposed for inferring the potential associations between miRNAs and diseases. However, these approaches ignore the importance of different relations in meta-paths when learning the embeddings of miRNAs and diseases. Besides, they pay little attention to screening out reliable negative samples which is crucial for improving the prediction accuracy. In this study, we propose a novel approach named MGCNSS with the multi-layer graph convolution and high-quality negative sample selection strategy. Specifically, MGCNSS first constructs a comprehensive heterogeneous network by integrating miRNA and disease similarity networks coupled with their known association relationships. Then, we employ the multi-layer graph convolution to automatically capture the meta-path relations with different lengths in the heterogeneous network and learn the discriminative representations of miRNAs and diseases. After that, MGCNSS establishes a highly reliable negative sample set from the unlabeled sample set with the negative distance-based sample selection strategy. Finally, we train MGCNSS under an unsupervised learning manner and predict the potential associations between miRNAs and diseases. The experimental results fully demonstrate that MGCNSS outperforms all baseline methods on both balanced and imbalanced datasets. More importantly, we conduct case studies on colon neoplasms and esophageal neoplasms, further confirming the ability of MGCNSS to detect potential candidate miRNAs. The source code is publicly available on GitHub https://github.com/15136943622/MGCNSS/tree/master.
    Mesh-Begriff(e) Humans ; MicroRNAs/genetics ; Algorithms ; Computational Biology/methods ; Software ; Colonic Neoplasms/genetics
    Chemische Substanzen MicroRNAs
    Sprache Englisch
    Erscheinungsdatum 2024-04-16
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2068142-2
    ISSN 1477-4054 ; 1467-5463
    ISSN (online) 1477-4054
    ISSN 1467-5463
    DOI 10.1093/bib/bbae168
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: The role of CXCL10 in prognosis of patients with colon cancer and tumor microenvironment remodeling.

    Song, Weiwei / Yin, Hongli / Han, Chenguang / Mao, Qiantai / Tang, Jing / Ji, Zhaoshuai / Yan, Xu / Wang, Lan / Liu, Shengnan / Ai, Chao

    Medicine

    2021  Band 100, Heft 38, Seite(n) e27224

    Abstract: Backgroung: Tumor microenvironment (TME) has gradually emerged as an important research topic in the fight against cancer. The immune system is a major contributing factor in TME, and investigations have revealed that tumors are partially infiltrated ... ...

    Abstract Backgroung: Tumor microenvironment (TME) has gradually emerged as an important research topic in the fight against cancer. The immune system is a major contributing factor in TME, and investigations have revealed that tumors are partially infiltrated with numerous immune cell subsets.
    Method: We obtained transcriptome RNA-seq data from the the Cancer Genome Atlas databases for 521 patients with colon adenocarcinoma (COAD). ESTIMATE algorithms are then used to estimate the fraction of stromal and immune cells in COAD samples.
    Result: A total of 1109 stromal-immune score-related differentially expressed genes were identified and used to generate a high-confidence protein-protein interaction network and univariate COX regression analysis. C-X-C motif chemokine 10 (CXCL10) was identified as the core gene by intersection analysis of data from protein-protein interaction network and univariate COX regression analysis. Then, for CXCL10, we performed gene set enrichment analysis, survival analysis and clinical analysis, and we used CIBERSORT algorithms to estimate the proportion of tumor-infiltrating immune cells in COAD samples.
    Conclusion: We discovered that CXCL10 levels could be effective for predicting the prognosis of COAD patients as well as a clue that the status of TME is transitioning from immunological to metabolic activity, which provided additional information for COAD therapies.
    Mesh-Begriff(e) Aged ; Biomarkers, Tumor/analysis ; Biomarkers, Tumor/blood ; Chemokine CXCL10/analysis ; Chemokine CXCL10/blood ; Chemokine CXCL10/pharmacology ; Colonic Neoplasms/complications ; Colonic Neoplasms/mortality ; Humans ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Prognosis ; Tumor Microenvironment
    Chemische Substanzen Biomarkers, Tumor ; CXCL10 protein, human ; Chemokine CXCL10
    Sprache Englisch
    Erscheinungsdatum 2021-09-03
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 80184-7
    ISSN 1536-5964 ; 0025-7974
    ISSN (online) 1536-5964
    ISSN 0025-7974
    DOI 10.1097/MD.0000000000027224
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: TIAM2 enhances non-small cell lung cancer cell invasion and motility.

    Zhao, Zheng-Yuan / Han, Chen-Guang / Liu, Jun-Tao / Wang, Chang-Lei / Wang, Yi / Cheng, Li-Ya

    Asian Pacific journal of cancer prevention : APJCP

    2013  Band 14, Heft 11, Seite(n) 6305–6309

    Abstract: Background: TIAM2, a Rac guanine nucleotide exchange factor, is closely associated with cell adherence and migration. Here, we aimed to investigate the role of TIAM2 in non-small cell lung cancer (NSCLC) cells.: Materials and methods: A small ... ...

    Abstract Background: TIAM2, a Rac guanine nucleotide exchange factor, is closely associated with cell adherence and migration. Here, we aimed to investigate the role of TIAM2 in non-small cell lung cancer (NSCLC) cells.
    Materials and methods: A small interference RNA (siRNA) was introduced to silence the expression of TIAM2. Invasion and motility assays were then performed to assess the invasion and motility potential of NSCLC cells. GST-pull down assays were used to detect activation of Rac1.
    Results: TIAM2 was highly expressed in NSCLC cells. Knockdown of TIAM2 inhibited the invasion and motility, and suppressed activation of Rac1. Further experiments demonstrated that knockdown of TIAM2 could up-regulate the expression of E-cadherin, and down- regulate the expression of MMP-3, Twist and Snail.
    Conclusions: Our data suggest that TIAM2 can promote invasion and motility of NSCLC cells. Activation of Rac1 and regulation of some EMT/invasion-related genes may be involved in the underlying processes.
    Mesh-Begriff(e) Cadherins/genetics ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/metabolism ; Carcinoma, Non-Small-Cell Lung/pathology ; Cell Line, Tumor ; Cell Movement/genetics ; Down-Regulation ; Epithelial-Mesenchymal Transition/genetics ; Gene Expression Regulation, Neoplastic ; Guanine Nucleotide Exchange Factors/biosynthesis ; Guanine Nucleotide Exchange Factors/genetics ; Humans ; Lung Neoplasms/genetics ; Lung Neoplasms/metabolism ; Lung Neoplasms/pathology ; Neoplasm Invasiveness ; Up-Regulation ; rac1 GTP-Binding Protein/biosynthesis ; rac1 GTP-Binding Protein/genetics
    Chemische Substanzen Cadherins ; Guanine Nucleotide Exchange Factors ; RAC1 protein, human ; TIAM2 protein, human ; rac1 GTP-Binding Protein (EC 3.6.5.2)
    Sprache Englisch
    Erscheinungsdatum 2013-12-25
    Erscheinungsland Thailand
    Dokumenttyp Journal Article
    ZDB-ID 2218955-5
    ISSN 2476-762X ; 1513-7368
    ISSN (online) 2476-762X
    ISSN 1513-7368
    DOI 10.7314/apjcp.2013.14.11.6305
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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