The Discovery of Compounds That Stimulate the Activity of Kallikrein-Related Peptidase 3 (KLK3)

被引:7
|
作者
Harkonen, Henna H. [1 ]
Mattsson, Johanna M. [2 ,3 ]
Maatta, Juha A. E. [4 ,5 ]
Stenman, Ulf-Hakan [2 ,3 ]
Koistinen, Hannu [2 ,3 ]
Matero, Sanni [6 ,7 ]
Windshugel, Bjorn [8 ]
Poso, Antti [1 ]
Lahtela-Kakkonen, Maija [1 ]
机构
[1] Univ Eastern Finland, Fac Hlth Sci, Sch Pharm, Kuopio 70211, Finland
[2] Univ Helsinki, Dept Clin Chem, Helsinki 00014, Finland
[3] Univ Helsinki, Cent Hosp, Helsinki 00014, Finland
[4] Univ Tampere, Inst Biomed Technol, Tampere 33014, Finland
[5] Tampere Univ Hosp, Tampere 33014, Finland
[6] Univ Copenhagen, Fac Pharmaceut Sci, Dept Pharmaceut & Analyt Chem, DK-2100 Copenhagen, Denmark
[7] Univ Copenhagen, Fac Hlth Sci, Dept Food Sci Qual & Technol, DK-1958 Frederiksberg C, Denmark
[8] European ScreeningPort GmbH, D-22525 Hamburg, Germany
基金
芬兰科学院;
关键词
angiogenesis; kallikrein; molecular modeling; peptides; virtual screening; PROSTATE-SPECIFIC ANTIGEN; ITERATIVE PARTIAL EQUALIZATION; HUMAN TISSUE KALLIKREINS; CRYSTAL-STRUCTURE; ORBITAL ELECTRONEGATIVITY; SERINE PROTEASES; SCANNING CALORIMETER; GENETIC ALGORITHM; STRUCTURAL BASIS; SEMINAL FLUID;
D O I
10.1002/cmdc.201100349
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Kallikrein-related peptidase 3 (KLK3), also known as prostate-specific antigen (PSA), is the most useful biomarker for prostate cancer (PCa). KLK3 is suggested to play a role in regulating cancer growth through anti-angiogenic activity in vivo and in vitro. This feature, together with its specificity for prostate tissue, makes KLK3 an intriguing target for the design of new therapies for PCa. 3D pharmacophores for KLK3-stimulating compounds were generated based on peptides that bind specifically to KLK3 and increase its enzymatic activity. As a result of pharmacophore-based virtual screening, four small, drug-like compounds with affinity for KLK3 were discovered and validated by capillary differential scanning calorimetry. One of the compounds also stimulated the activity of KLK3, and is therefore the first published small molecule with such an activity.
引用
收藏
页码:2170 / 2178
页数:9
相关论文
共 50 条
  • [1] Virtual Screening of Small Drug-Like Compounds Stimulating the Enzymatic Activity of Kallikrein-Related Peptidase3 (KLK3)
    Ylikangas, Henna
    Mattsson, Johanna M.
    Stenman, Ulf-Hakan
    Koistinen, Hannu
    Poso, Antti
    Lahtela-Kakkonen, Maija
    CHEMMEDCHEM, 2016, 11 (18) : 2043 - 2049
  • [2] Substrate specificity and inhibition of human kallikrein-related peptidase 3 (KLK3 or PSA) activated with sodium citrate and glycosaminoglycans
    Andrade, Douglas
    Assis, Diego M.
    Lima, Aurelio Resende
    Oliveira, Juliana R.
    Araujo, Mariana S.
    Blaber, Sachiko I.
    Blaber, Michael
    Juliano, Maria A.
    Juliano, Luiz
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2010, 498 (01) : 74 - 82
  • [3] Gene expression changes associated with the anti-angiogenic activity of kallikrein-related peptidase 3 (KLK3) on human umbilical vein endothelial cells
    Mattsson, Johanna M.
    Laakkonen, Pirjo
    Kilpinen, Sami
    Stenman, Ulf-Hakan
    Koistinen, Hannu
    BIOLOGICAL CHEMISTRY, 2008, 389 (06) : 765 - 771
  • [4] Upregulation and secretion of kallikrein-related peptidase 6 (KLK6) in gastric cancer
    Kim, Jin Ju
    Kim, Jong-Tae
    Yoon, Hyo Ran
    Kang, Min Ah
    Kim, Joo Heon
    Lee, Young-Ha
    Kim, Jae Wha
    Lee, Seon-Jin
    Song, Eun Young
    Myung, Pyung Keun
    Lee, Hee Gu
    TUMOR BIOLOGY, 2012, 33 (03) : 731 - 738
  • [5] Kallikrein-related peptidase 14 is the second KLK protease targeted by the serpin vaspin
    Ulbricht, David
    Tindall, Catherine A.
    Oertwig, Kathrin
    Hanke, Stefanie
    Straeter, Norbert
    Heiker, John T.
    BIOLOGICAL CHEMISTRY, 2018, 399 (09) : 1079 - 1084
  • [6] The physiology and pathobiology of human kallikrein-related peptidase 6 (KLK6)
    Bayani, Jane
    Diamandis, Eleftherios P.
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2012, 50 (02) : 211 - 233
  • [7] Specificity studies on Kallikrein-related peptidase 7 (KLK7) and effects of osmolytes and glycosaminoglycans on its peptidase activity
    Oliveira, Juliana R.
    Bertolin, Thiago C.
    Andrade, Douglas
    Oliveira, Lilian C. G.
    Kondo, Marcia Y.
    Santos, Jorge A. N.
    Blaber, Michael
    Juliano, Luiz
    Severino, Beatrice
    Caliendo, Giuseppe
    Santagada, Vincenzo
    Juliano, Maria A.
    BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2015, 1854 (01): : 73 - 83
  • [8] Pseudopeptides with a centrally positioned alkene-based disulphide bridge mimetic stimulate kallikrein-related peptidase 3 activity
    Meinander, Kristian
    Weisell, Janne
    Pakkala, Miikka
    Tadd, Andrew C.
    Hekim, Can
    Kallionpaa, Roope
    Widell, Kim
    Stenman, Ulf-Hakan
    Koistinen, Hannu
    Narvanen, Ale
    Vepsalainen, Jouko
    Luthman, Kristina
    Wallen, Erik A. A.
    MEDCHEMCOMM, 2013, 4 (03) : 549 - 553
  • [9] Enzymatic properties of human kallikrein-related peptidase 12 (KLK12)
    Memari, Nader
    Jiang, Weiping
    Diamandis, Eleftherios P.
    Luo, Liu-Ying
    BIOLOGICAL CHEMISTRY, 2007, 388 (04) : 427 - 435
  • [10] Using kallikrein-related peptidases (KLK) as novel cancer biomarkers
    Schmitt, Manfred
    Magdolen, Viktor
    THROMBOSIS AND HAEMOSTASIS, 2009, 101 (02) : 222 - 224