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      KCI등재 SCIE SCOPUS

      Diagnostic Significance of p38 Isoforms (p38α, p38β, p38γ, p38δ) in Head and Neck Squamous Cell Carcinoma: Comparative Serum Level Evaluation and Design of Novel Peptide Inhibitor Targeting the Same

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      https://www.riss.kr/link?id=A105988219

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      다국어 초록 (Multilingual Abstract)

      Purpose The p38 mitogen-activated protein kinase (MAPKs) play a crucial role in the production of pro-inflammatory cytokines and over-expression of it increase cytokines which promote cancer. Among four isoforms, p38α has been well studied in head an...

      Purpose The p38 mitogen-activated protein kinase (MAPKs) play a crucial role in the production of pro-inflammatory cytokines and over-expression of it increase cytokines which promote cancer.
      Among four isoforms, p38α has been well studied in head and neck squamous cell carcinoma (HNSCC) and other cancers as a therapeutic target. p38δ has recently emerged as a potential disease-specific drug target. Elevated serum p38α level in HNSCC was reported earlier from our lab. This study aims to estimate the levels of p38 MAPK-isoforms in the serum of HNSCC and design peptide inhibitor targeting the same.
      Materials and Methods Levels of p38 MAPK isoforms in the serum of HNSCC and healthy controls were quantified by surface plasmon resonance technology. The peptide inhibitor for p38 MAPK was designed by molecular modeling using Grid-based Ligand Docking with Energetics tools and compared with known specific inhibitors.
      Results We have observed highly elevated levels of all four isoforms of p38 MAPK in serum of HNSCC patients compared to the control group. Further, serum p38α, p38β, and p38δ levels were down regulated after therapy in follow-up patients, while p38γ showed no response to the therapy. Present study screened designed peptide WFYH as a specific inhibitor against p38δ. The specific inhibitor of p38δ was found to have no effect on p38α due to great structural difference at ATP binding pocket.
      Conclusion In this study, first time estimated the levels of p38 MAPK isoforms in the serum of HNSCC.
      It can be concluded that p38 MAPK isoforms can be a diagnostic and prognostic marker for HNSCC and p38δ as a therapeutic target.

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      참고문헌 (Reference)

      1 Singh AK, "p38beta MAP kinase as a therapeutic target for pancreatic cancer" 80 : 266-273, 2012

      2 Lee JC, "p38 mitogenactivated protein kinase inhibitors : mechanisms and therapeutic potentials" 82 : 389-397, 1999

      3 Hawkins J, "p38 map kinase substrate specificity differs greatly for protein and peptide substrates" 382 : 310-313, 2000

      4 Azevedo R, "X-ray structure of p38 bound to TAK-715:comparison with three classic inhibitors" 68 (68): 1041-1050, 2012

      5 Bellon S, "The structure of phosphorylated p38gamma is monomeric and reveals a conserved activation-loop conformation" 7 : 1057-1065, 1999

      6 Gill K, "The rational design of specific peptide inhibitor against p38alpha MAPK at allosteric-site: a therapeutic modality for HNSCC" 9 : e101525-, 2014

      7 Yurtsever Z, "The crystal structure of phosphorylated MAPK13 reveals common structural features and differences in p38 MAPK family activation" 71 (71): 790-799, 2015

      8 Fitzgerald CE, "Structural basis for p38alpha MAP kinase quinazolinone and pyridol-pyrimidine inhibitor specificity" 10 : 764-769, 2003

      9 Gill K, "Quantification of p38alphaMAP kinase : a prognostic marker in HNSCC with respect to radiation therapy" 413 : 219-225, 2012

      10 Kamangar F, "Patterns of cancer incidence, mortality, and prevalence across five continents : defining priorities to reduce cancer disparities in different geographic regions of the world" 24 : 2137-2150, 2006

      1 Singh AK, "p38beta MAP kinase as a therapeutic target for pancreatic cancer" 80 : 266-273, 2012

      2 Lee JC, "p38 mitogenactivated protein kinase inhibitors : mechanisms and therapeutic potentials" 82 : 389-397, 1999

      3 Hawkins J, "p38 map kinase substrate specificity differs greatly for protein and peptide substrates" 382 : 310-313, 2000

      4 Azevedo R, "X-ray structure of p38 bound to TAK-715:comparison with three classic inhibitors" 68 (68): 1041-1050, 2012

      5 Bellon S, "The structure of phosphorylated p38gamma is monomeric and reveals a conserved activation-loop conformation" 7 : 1057-1065, 1999

      6 Gill K, "The rational design of specific peptide inhibitor against p38alpha MAPK at allosteric-site: a therapeutic modality for HNSCC" 9 : e101525-, 2014

      7 Yurtsever Z, "The crystal structure of phosphorylated MAPK13 reveals common structural features and differences in p38 MAPK family activation" 71 (71): 790-799, 2015

      8 Fitzgerald CE, "Structural basis for p38alpha MAP kinase quinazolinone and pyridol-pyrimidine inhibitor specificity" 10 : 764-769, 2003

      9 Gill K, "Quantification of p38alphaMAP kinase : a prognostic marker in HNSCC with respect to radiation therapy" 413 : 219-225, 2012

      10 Kamangar F, "Patterns of cancer incidence, mortality, and prevalence across five continents : defining priorities to reduce cancer disparities in different geographic regions of the world" 24 : 2137-2150, 2006

      11 Risco A, "New insights into the p38gamma and p38delta MAPK pathways" 2012 : 520289-, 2012

      12 Enslen H, "Molecular determinants that mediate selective activation of p38 MAP kinase isoforms" 19 : 1301-1311, 2000

      13 Halgren TA, "Glide: a new approach for rapid, accurate docking and scoring. 2. Enrichment factors in database screening" 47 : 1750-1759, 2004

      14 Gill K, "Development of peptide inhibitor as a therapeutic agent against head and neck squamous cell carcinoma(HNSCC)targeting p38alpha MAP kinase" 1830 : 2763-2769, 2013

      15 Dougherty DA, "Cation-pi interactions in chemistry and biology : a new view of benzene, Phe, Tyr, and Trp" 271 : 163-168, 1996

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2024 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2021-01-01 평가 등재학술지 선정 (해외등재 학술지 평가) KCI등재
      2020-12-01 평가 등재후보로 하락 (해외등재 학술지 평가) KCI등재후보
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-05-27 학술지명변경 한글명 : 대한암학회지 -> Cancer Research and Treatment KCI등재
      2005-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 3.58 0.89 3.01
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      2.62 2.28 1.846 0.26
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