메뉴 건너뛰기




Volumn 98, Issue , 2014, Pages 190-196

Two structurally distinct chalcone dimers from Helichrysum zivojinii and their activities in cancer cell lines

Author keywords

Asteraceae; Chalcone glucoside dimers; Drug combination; Flavonoid glucoside; Helichrysum zivojinii; HIF 1 ; MAP kinase pathway; Topoisomerase II

Indexed keywords

ASTERACEAE; HELICHRYSUM;

EID: 84892946345     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2013.11.025     Document Type: Article
Times cited : (26)

References (49)
  • 1
    • 70349845903 scopus 로고    scopus 로고
    • Compositions, antioxidant and antimicrobial activities of Helichrysum (Asteraceae) species collected from Turkey
    • S. Albayrak, A. Aksoy, O. Sagdic, and E. Hamzaoglu Compositions, antioxidant and antimicrobial activities of Helichrysum (Asteraceae) species collected from Turkey Food Chem. 119 2010 114 122
    • (2010) Food Chem. , vol.119 , pp. 114-122
    • Albayrak, S.1    Aksoy, A.2    Sagdic, O.3    Hamzaoglu, E.4
  • 2
    • 2642690680 scopus 로고    scopus 로고
    • Correlation between multidrug resistance and the degree of differentiation of non-small-cell bronchopulmonary carcinoma (NSCLC) in vitro and in vivo
    • S. Bosch, S. Siavoshian, C. Jacquot, C. Tomasoni, G. Dabouis, Y. Elanbaloussi, T. Leneel, M.T. More, and C. Roussakis Correlation between multidrug resistance and the degree of differentiation of non-small-cell bronchopulmonary carcinoma (NSCLC) in vitro and in vivo Anticancer Res. 17 1997 4595 4598 (Pubitemid 28081750)
    • (1997) Anticancer Research , vol.17 , Issue.6 D , pp. 4595-4598
    • Bosch, S.1    Siavoshian, S.2    Jacquot, C.3    Tomasoni, C.4    Dabouis, G.5    Elanbaloussi, Y.6    Leneel, T.7    More, M.T.8    Roussakis, C.9
  • 5
    • 0031304677 scopus 로고    scopus 로고
    • Evaluation of three rapid RNA extraction reagents: Relevance for use in RTPCR's and measurement of low level gene expression in clinical samples
    • T. Chadderton, C. Wilson, M. Bewick, and S. Gluck Evaluation of three rapid RNA extraction reagents: relevance for use in RTPCR's and measurement of low level gene expression in clinical samples Cell Mol. Biol. 43 1997 1227 1234
    • (1997) Cell Mol. Biol. , vol.43 , pp. 1227-1234
    • Chadderton, T.1    Wilson, C.2    Bewick, M.3    Gluck, S.4
  • 6
    • 0021118703 scopus 로고
    • Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
    • T.C. Chou, and P. Talalay Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors Adv. Enzyme Regul. 22 1984 27 55
    • (1984) Adv. Enzyme Regul. , vol.22 , pp. 27-55
    • Chou, T.C.1    Talalay, P.2
  • 8
    • 0027377610 scopus 로고
    • Choleretic effect of the essential oil from Helichrysum picardii Boiss. and Reuter in rats
    • R. de la Puerta, M.T. Saenz, and M.D. Garcia Choleretic effect of the essential oil from Helichrysum picardii Boiss and Reuter in rats Phytother. Res. 7 1993 376 377 (Pubitemid 23290735)
    • (1993) Phytotherapy Research , vol.7 , Issue.5 , pp. 376-377
    • De La Puerta, R.1    Saenz, M.T.2    Garcia, M.D.3
  • 11
    • 0035849168 scopus 로고    scopus 로고
    • Identification of a sucrose diester of a substituted β-truxinic acid in oats
    • DOI 10.1016/S0031-9422(00)00505-7, PII S0031942200005057
    • L.H. Dimberg, R.E. Andersson, S. Gohil, S. Bryngelsson, and L.N. Lundgren Identification of a sucrose diester of a substituted b-truxinic acid in oats Phytochemistry 56 2001 843 847 (Pubitemid 32288994)
    • (2001) Phytochemistry , vol.56 , Issue.8 , pp. 843-847
    • Dimberg, L.H.1    Andersson, R.E.2    Gohil, S.3    Bryngelsson, S.4    Lundgren, L.N.5
  • 12
    • 78449235744 scopus 로고    scopus 로고
    • Compositae (pro parte majore)
    • Greuter, W. & Raab-Straube, E. von (ed.) Helichrysum zivojinii Černjavski & Soška. Accessed through: Euro+Med
    • Greuter, W. (2006-2009): Compositae (pro parte majore). - In: Greuter, W. & Raab-Straube, E. von (ed.): Compositae. Euro+Med Plantbase - the information resource for Euro-Mediterranean plant diversity. Helichrysum zivojinii Černjavski & Soška. Accessed through: Euro+Med.
    • (2006) Compositae. Euro+Med Plantbase - The Information Resource for Euro-Mediterranean Plant Diversity
    • Greuter, W.1
  • 13
    • 78651120654 scopus 로고
    • The separation of (+)-naringenin 5-β-d-monoglucoside from salipurposide
    • R. Haensel, D. Heise, H. Rimpler, and G. Pinkewitz The separation of (+)-naringenin 5-β-d-monoglucoside from salipurposide Arch. Pharm. 296 1963 468 474
    • (1963) Arch. Pharm. , vol.296 , pp. 468-474
    • Haensel, R.1    Heise, D.2    Rimpler, H.3    Pinkewitz, G.4
  • 14
    • 0031080932 scopus 로고    scopus 로고
    • Unusual biflavonoids in the farinose exudate of Pentagramma triangularis
    • DOI 10.1016/S0031-9422(96)00597-3, PII S0031942296005973
    • M. Iinuma, Y. Kakuto, N. Tanida, T. Tanaka, and F.A. Lang Unusual biflavonoids in the farinose exudates of Pentagramma triangularis Phytochemistry 44 4 1997 705 710 (Pubitemid 27073876)
    • (1997) Phytochemistry , vol.44 , Issue.4 , pp. 705-710
    • Iinuma, M.1    Kakuto, Y.2    Tanida, N.3    Tanaka, T.4    Lang, F.A.5
  • 15
    • 1642546987 scopus 로고    scopus 로고
    • Dimeric Flavonol Glycoside and Galloylated C-Glucosylchromones from Kunzea ambigua
    • DOI 10.1021/np030367s
    • H. Ito, N. Kasajima, H. Tokuda, H. Nishino, and T. Yoshida Dimeric flavonol glycoside and galloylated C-glucosylchromones from Kunzea ambigua J. Nat. Prod. 67 2004 411 415 (Pubitemid 38405704)
    • (2004) Journal of Natural Products , vol.67 , Issue.3 , pp. 411-415
    • Ito, H.1    Kasajima, N.2    Tokuda, H.3    Nishino, H.4    Yoshida, T.5
  • 16
    • 70749109630 scopus 로고    scopus 로고
    • Chalcone glycoside in the flowers of six corylopsis species as yellow pigment
    • T. Iwashina, T. Takemura, and T. Mishio Chalcone glycoside in the flowers of six corylopsis species as yellow pigment J. Jpn. Soc. Hort. Sci. 78 2009 485 490
    • (2009) J. Jpn. Soc. Hort. Sci. , vol.78 , pp. 485-490
    • Iwashina, T.1    Takemura, T.2    Mishio, T.3
  • 17
    • 19544366753 scopus 로고    scopus 로고
    • Isolation and synthesis of a dimeric dihydrochalcone from Agapanthus africanus
    • DOI 10.1016/j.phytochem.2005.04.007, PII S0031942205001627
    • B.I. Kamara, D.T.L. Manong, and E.V. Brandt Isolation and synthesis of a dimeric dihydrochalcone from Agapanthus africanus Phytochemistry 66 2005 1126 1132 (Pubitemid 40728306)
    • (2005) Phytochemistry , vol.66 , Issue.10 , pp. 1126-1132
    • Kamara, B.I.1    Manong, D.T.L.2    Brandt, E.V.3
  • 18
    • 0842284356 scopus 로고    scopus 로고
    • Cyclobutanes from Combretum albopunctatum
    • DOI 10.1016/j.phytochem.2003.09.014
    • D.R. Katerere, A.I. Gray, A.R. Kennedy, R.J. Nash, and R.D. Waigh Cyclobutanes from Combretum albopunctatum Phytochemistry 65 2004 433 438 (Pubitemid 38169142)
    • (2004) Phytochemistry , vol.65 , Issue.4 , pp. 433-438
    • Katerere, D.R.1    Gray, A.I.2    Kennedy, A.R.3    Nash, R.J.4    Waigh, R.D.5
  • 20
    • 70349337628 scopus 로고    scopus 로고
    • Antihyperglycemic activity of phenylpropanoyl esters of catechol glycoside and its dimers from Dodecadenia grandiflora
    • M. Kumar, P. Rawat, N. Rahuja, A.K. Srivastava, and R. Maurya Antihyperglycemic activity of phenylpropanoyl esters of catechol glycoside and its dimers from Dodecadenia grandiflora Phytochemistry 70 2009 1448 1455
    • (2009) Phytochemistry , vol.70 , pp. 1448-1455
    • Kumar, M.1    Rawat, P.2    Rahuja, N.3    Srivastava, A.K.4    Maurya, R.5
  • 21
    • 53449095404 scopus 로고    scopus 로고
    • South African Helichrysum species: A review of the traditional uses, biological activity and phytochemistry
    • A.C.U. Lourens, A.M. Viljoen, and F.R. van Heerden South African Helichrysum species: a review of the traditional uses, biological activity and phytochemistry J. Ethnopharmacol. 119 2008 630 652
    • (2008) J. Ethnopharmacol. , vol.119 , pp. 630-652
    • Lourens, A.C.U.1    Viljoen, A.M.2    Van Heerden, F.R.3
  • 22
    • 0344075992 scopus 로고    scopus 로고
    • The polyphenol constituents of grape pomace
    • DOI 10.1016/S0308-8146(98)00245-3, PII S0308814698002453
    • Y. Lu, and L.Y. Foo The polyphenol constituents of grape pomace Food Chem. 65 1999 1 8 (Pubitemid 29076689)
    • (1999) Food Chemistry , vol.65 , Issue.1 , pp. 1-8
    • Lu, Y.1    Yeap Foo, L.2
  • 25
    • 84886856412 scopus 로고    scopus 로고
    • Cancer-suppressive potential of extracts of endemic plant Helichrysum zivojinii: Effects on cell migration, invasion and angiogenesis
    • I. Matić, I. Aljančić, V. Vajs, M. Jadranin, N. Gligorijević, S. Milosavljević, and Z. Juranić Cancer-suppressive potential of extracts of endemic plant Helichrysum zivojinii: effects on cell migration, invasion and angiogenesis Nat. Prod. Commun. 8 2013 1291 1296
    • (2013) Nat. Prod. Commun. , vol.8 , pp. 1291-1296
    • Matić, I.1    Aljančić, I.2    Vajs, V.3    Jadranin, M.4    Gligorijević, N.5    Milosavljević, S.6    Juranić, Z.7
  • 26
    • 0029065123 scopus 로고
    • Antibacterial activity of Helichrysum aureonintens (Asteraceae)
    • J.J. Meyer, and A.J. Afolayan Antibacterial activity of Helichrysum aureonintens (Asteraceae) J. Ethnopharmacol. 47 1995 109 111
    • (1995) J. Ethnopharmacol. , vol.47 , pp. 109-111
    • Meyer, J.J.1    Afolayan, A.J.2
  • 27
    • 0001617168 scopus 로고
    • Structure and confirmation of chalcone photodimers and related compounds
    • G. Montaudo, and S. Caccamese Structure and confirmation of chalcone photodimers and related compounds J. Org. Chem. 38 1973 710 715
    • (1973) J. Org. Chem. , vol.38 , pp. 710-715
    • Montaudo, G.1    Caccamese, S.2
  • 28
    • 84994995324 scopus 로고
    • Photodimers of cinnamic acid and related compounds. A stereochemical study by NMR
    • G. Montaudo, S. Caccamese, and V. Librando Photodimers of cinnamic acid and related compounds. A stereochemical study by NMR Org. Magn. Reson. 6 1974 534 536
    • (1974) Org. Magn. Reson. , vol.6 , pp. 534-536
    • Montaudo, G.1    Caccamese, S.2    Librando, V.3
  • 30
    • 61349121467 scopus 로고    scopus 로고
    • Inhibition of HIF-1alpha activity by homeodomain-interacting protein kinase-2 correlates with sensitization of chemoresistant cells to undergo apoptosis
    • 10.1186/1476-4598-8-117
    • L. Nardinocchi, R. Puca, A. Sacchi, and G. D'Orazi Inhibition of HIF-1alpha activity by homeodomain-interacting protein kinase-2 correlates with sensitization of chemoresistant cells to undergo apoptosis Mol. Cancer 8 2009 10.1186/1476-4598-8-117
    • (2009) Mol. Cancer , vol.8
    • Nardinocchi, L.1    Puca, R.2    Sacchi, A.3    D'Orazi, G.4
  • 32
    • 0033046903 scopus 로고    scopus 로고
    • Altered expression of mRNAs for apoptosis-modulating proteins in a low level multidrug resistant variant of a human lung carcinoma cell line that also expresses mdr1 mRNA
    • DOI 10.1002/(SICI)1097-0215(19990730)82:3<368::AID-IJC10>3.0.CO;2-E
    • R. NicAmhlaoibh, M. Heenan, I. Cleary, S. Touhey, C. O'Loughlin, C. Daly, G. Nunez, K.J. Scanlon, and M. Clynes Altered expression of mRNAs for apoptosys-modulating proteins in a low level multidrug resistant variant of a human lung carcinoma cell line that also expresses mdr1 mRNA Int. J. Cancer 82 1999 368 376 (Pubitemid 29302978)
    • (1999) International Journal of Cancer , vol.82 , Issue.3 , pp. 368-376
    • Nicamhlaoibh, R.1    Heenan, M.2    Cleary, I.3    Touhey, S.4    O'Loughlin, C.5    Daly, C.6    Nunez, G.7    Scanlon, K.J.8    Clynes, M.9
  • 33
    • 35348951512 scopus 로고    scopus 로고
    • Pauferrol A, a novel chalcone trimer with a cyclobutane ring from Caesalpinia ferrea mart exhibiting DNA topoisomerase II inhibition and apoptosis-inducing activity
    • DOI 10.1016/j.tetlet.2007.09.130, PII S004040390701920X
    • N. Nozaki, K. Hayashi, M. Kido, K. Kakumoto, S. Ikeda, N. Matsuura, H. Tani, D. Takaoka, M. Iinumae, and Y. Akaof Pauferrol A, a novel chalcone trimer with a cyclobutane ring from Caesalpinia ferrea Mart exhibiting NA topoisomerase II inhibition and apoptosis-inducing activity Tetrahedron Lett. 48 2007 8290 8292 (Pubitemid 47615099)
    • (2007) Tetrahedron Letters , vol.48 , Issue.47 , pp. 8290-8292
    • Nozaki, H.1    Hayashi, K.-i.2    Kido, M.3    Kakumoto, K.4    Ikeda, S.5    Matsuura, N.6    Tani, H.7    Takaoka, D.8    Iinuma, M.9    Akao, Y.10
  • 35
    • 0027400535 scopus 로고
    • New triterpenes and flavonoids from the leaves of Bosistoa Brassii
    • I.C. Parsons, A.I. Gray, P.G. Waterman, and T.G. Hartley New triterpenes and flavonoids from the leaves of Bosistoa Brassii J. Nat. Prod. 56 1993 46 63
    • (1993) J. Nat. Prod. , vol.56 , pp. 46-63
    • Parsons, I.C.1    Gray, A.I.2    Waterman, P.G.3    Hartley, T.G.4
  • 37
    • 0000809881 scopus 로고
    • Apigenin-7-glucoside and its acetates 2″- and 6″-acetates from ligulate flowers of Matricaria chamomilla
    • C. Redaelli, L. Formentini, and E. Santaniello Apigenin-7-glucoside and its acetates 2″- and 6″-acetates from ligulate flowers of Matricaria chamomilla Phytochemistry 19 1980 985 986
    • (1980) Phytochemistry , vol.19 , pp. 985-986
    • Redaelli, C.1    Formentini, L.2    Santaniello, E.3
  • 39
    • 0011780757 scopus 로고
    • Methylene bisflavonoids from frond exudate of Pentagramma triangularis ssp. Triangularis
    • J.N. Roitman, R.Y. Wong, and E. Wollenweber Methylene bisflavonoids from frond exudate of Pentagramma triangularis ssp. triangularis Phytochemistry 34 1993 297 301
    • (1993) Phytochemistry , vol.34 , pp. 297-301
    • Roitman, J.N.1    Wong, R.Y.2    Wollenweber, E.3
  • 40
    • 0034727535 scopus 로고    scopus 로고
    • (Rel)-1b,2a-di-(2,4-dihydroxy-6-methoxybenzoyl)-3b,4a-di-(4- methoxyphenyl)-cyclobutane and other flavonoids from the aerial parts of Goniothalamus gardneri and Goniothalamus thwaitesii
    • V. Seidel, F. Bailleul, and P.G. Waterman (Rel)-1b,2a-di-(2,4-dihydroxy- 6-methoxybenzoyl)-3b,4a-di-(4-methoxyphenyl)-cyclobutane and other flavonoids from the aerial parts of Goniothalamus gardneri and Goniothalamus thwaitesii Phytochemistry 55 2000 439 446
    • (2000) Phytochemistry , vol.55 , pp. 439-446
    • Seidel, V.1    Bailleul, F.2    Waterman, P.G.3
  • 42
    • 0028798496 scopus 로고
    • Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies
    • R. Slimestad, ∅.M. Andersen, G.W. Francis, A. Marston, and K. Hostettmann Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies Phytochemistry 40 1995 1537 1542
    • (1995) Phytochemistry , vol.40 , pp. 1537-1542
    • Slimestad, R.1    Andersen, M.2    Francis, G.W.3    Marston, A.4    Hostettmann, K.5
  • 43
    • 84860480401 scopus 로고    scopus 로고
    • Signal transduction pathways and transcriptional mechanisms of ABCB1/Pgp-mediated multiple drug resistance in human cancer cells
    • H. Sui, Z.Z. Fan, and Q. Li Signal transduction pathways and transcriptional mechanisms of ABCB1/Pgp-mediated multiple drug resistance in human cancer cells J. Int. Med. Res. 40 2012 426 435
    • (2012) J. Int. Med. Res. , vol.40 , pp. 426-435
    • Sui, H.1    Fan, Z.Z.2    Li, Q.3
  • 46
    • 0028151418 scopus 로고
    • Monitoring mRNA expression by polymerase chain reaction: The "primer-dropping" method
    • H. Wong, W.D. Anderson, T. Cheng, and K.T. Riabowol Monitoring mRNA expression by polymerase chain reaction: the "primer-dropping" method Anal. Biochem. 223 1994 251 258
    • (1994) Anal. Biochem. , vol.223 , pp. 251-258
    • Wong, H.1    Anderson, W.D.2    Cheng, T.3    Riabowol, K.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.