Quercetin, Siamois 1 and siamois 2 induce apoptosis in human breast cancer MDA-MB-435 cells xenograft in vivo

We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells xenografted in athymic nude mice. This study clearly demonstrated that these compounds exhibited apoptosis-inducing activities in cell cultur...

Full description

Saved in:
Bibliographic Details
Published inCancer biology & therapy Vol. 6; no. 1; pp. 56 - 61
Main Authors Dechsupa, Samarn, Kothan, Suchart, Vergote, Jackie, Leger, Gerard, Martineau, Antoine, Beranger, Simone, Kosanlavit, Rachian, Moretti, Jean-Luc, Mankhetkorn, Samlee
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 01.01.2007
Subjects
Online AccessGet full text

Cover

Loading…
Abstract We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells xenografted in athymic nude mice. This study clearly demonstrated that these compounds exhibited apoptosis-inducing activities in cell culture system. Quercetin (20 μg/mL), Siamois 1 (100 μg/mL), and Siamois 2 (200 μg/mL) can induce apoptotic cell death by 40± 5%, 44 ± 14 %, and 31 ± 13 %, respectively. Two-fold of IC50 of these compounds were clearly found to induce apoptosis in breast tumor tissue which can be determined by 99m Tc-annexin V scintigraphy and histological staining. This is the first report that the apoptosis-inducing effects of quercetin, Siamois 1, and Siamois 2 on the MDA-MB 435 cell in vitro were effectively extrapolated to the in vivo situation. These compounds might be considered as a simple dietary supplement and with further clinical investigation for their use as a nutrition-based intervention in breast cancer treatment.
AbstractList We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells xenografted in athymic nude mice. This study clearly demonstrated that these compounds exhibited apoptosis-inducing activities in cell culture system. Quercetin (20 μg/mL), Siamois 1 (100 μg/mL), and Siamois 2 (200 μg/mL) can induce apoptotic cell death by 40± 5%, 44 ± 14 %, and 31 ± 13 %, respectively. Two-fold of IC50 of these compounds were clearly found to induce apoptosis in breast tumor tissue which can be determined by 99m Tc-annexin V scintigraphy and histological staining. This is the first report that the apoptosis-inducing effects of quercetin, Siamois 1, and Siamois 2 on the MDA-MB 435 cell in vitro were effectively extrapolated to the in vivo situation. These compounds might be considered as a simple dietary supplement and with further clinical investigation for their use as a nutrition-based intervention in breast cancer treatment.
We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells xenografted in athymic nude mice. This study clearly demonstrated that these compounds exhibited apoptosis-inducing activities in cell culture system. Quercetin (20 μg/mL), Siamois 1 (100 μg/mL), and Siamois 2 (200 μg/mL) can induce apoptotic cell death by 40± 5%, 44 ± 14 %, and 31 ± 13 %, respectively. Two-fold of IC50 of these compounds were clearly found to induce apoptosis in breast tumor tissue which can be determined by 99mTc-annexin V scintigraphy and histological staining. This is the first report that the apoptosis-inducing effects of quercetin, Siamois 1, and Siamois 2 on the MDA-MB 435 cell in vitro were effectively extrapolated to the in vivo situation. These compounds might be considered as a simple dietary supplement and with further clinical investigation for their use as a nutrition-based intervention in breast cancer treatment.
We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells xenografted in athymic nude mice. This study clearly demonstrated that these compounds exhibited apoptosis-inducing activities in cell culture system. Quercetin (20 microg/mL), Siamois 1 (100 microg/mL), and Siamois 2 (200 microg/mL) can induce apoptotic cell death by 40 +/-5%, 44 +/- 14 %, and 31 +/- 13 %, respectively. Two-fold of IC50 of these compounds were clearly found to induce apoptosis in breast tumor tissue which can be determined by 99mTc-Annexin V scintigraphy and histological staining. This is the first report that the apoptosis-inducing effects of quercetin, Siamois 1 and Siamois 2 on the MDA-MB 435 cell in vitro were effectively extrapolated to the in vivo situation. These compounds might be considered as a simple dietary supplement and with further clinical investigation for their use as a nutrition-based intervention in breast cancer treatment.
Author Dechsupa, Samarn
Beranger, Simone
Leger, Gerard
Moretti, Jean-Luc
Kothan, Suchart
Kosanlavit, Rachian
Vergote, Jackie
Mankhetkorn, Samlee
Martineau, Antoine
Author_xml – sequence: 1
  givenname: Samarn
  surname: Dechsupa
  fullname: Dechsupa, Samarn
– sequence: 2
  givenname: Suchart
  surname: Kothan
  fullname: Kothan, Suchart
– sequence: 3
  givenname: Jackie
  surname: Vergote
  fullname: Vergote, Jackie
– sequence: 4
  givenname: Gerard
  surname: Leger
  fullname: Leger, Gerard
– sequence: 5
  givenname: Antoine
  surname: Martineau
  fullname: Martineau, Antoine
– sequence: 6
  givenname: Simone
  surname: Beranger
  fullname: Beranger, Simone
– sequence: 7
  givenname: Rachian
  surname: Kosanlavit
  fullname: Kosanlavit, Rachian
– sequence: 8
  givenname: Jean-Luc
  surname: Moretti
  fullname: Moretti, Jean-Luc
– sequence: 9
  givenname: Samlee
  surname: Mankhetkorn
  fullname: Mankhetkorn, Samlee
BackLink https://www.ncbi.nlm.nih.gov/pubmed/17172819$$D View this record in MEDLINE/PubMed
BookMark eNptkEtP3DAURq0KVGDaXdeVfwCZxvEjniXl1UoghGjX1o1zTV0l9sjOUObf42imsGHlh879dL9zQg5CDEjIF1YvBVPsm-2mpVqyJZdCfyDHTEpZadmqg_nOdSVq0R6Rk5z_1nXTNmr1kRyxlrWNZqtjMt5vMFmcfDilDx7G6DNlFEJP8_7VUB_6jUUK67ieYi5fPtA_mxEC7RJCnqiFYDHR24uz6vZ7JbikFoch02cM8TGBm-aJJ_8UP5FDB0PGz_tzQX5fXf46_1Hd3F3_PD-7qWypNFW94yBsI3Tp0gNwrRCtXtWKCSt60XSomXVWriTv0AHjSitoLBPokNdS8wU53eXaFHNO6Mw6-RHS1rDazNZMsWaUYWa2VvCvO3y96Ubs3-C9pgLUO2AoZjB3PmbrsZR-Rec8SJO3A_7PbHcjPriYRvgX09CbCbZDTC4VYT4b_u42L_l5ju0
CitedBy_id crossref_primary_10_46332_aemj_1005558
crossref_primary_10_1016_j_heliyon_2019_e02052
crossref_primary_10_1016_j_tox_2008_04_001
crossref_primary_10_3844_ajptsp_2010_24_33
crossref_primary_10_1016_j_pharep_2014_12_010
crossref_primary_10_1155_2016_8434308
crossref_primary_10_1038_s41598_018_21516_5
crossref_primary_10_1016_j_ejpb_2011_04_011
crossref_primary_10_1021_jf900259m
crossref_primary_10_1593_tlo_07100
crossref_primary_10_1016_j_colsurfb_2020_111341
crossref_primary_10_1016_j_nut_2018_06_018
crossref_primary_10_1186_1476_4598_9_99
crossref_primary_10_34172_jhp_2024_48087
crossref_primary_10_1016_j_cyto_2012_07_020
crossref_primary_10_1039_b801558a
crossref_primary_10_2174_1573401319666230428152045
crossref_primary_10_1186_s10020_018_0032_7
crossref_primary_10_1016_j_foodchem_2007_11_037
crossref_primary_10_1021_mp4003464
crossref_primary_10_1016_j_lfs_2020_117463
crossref_primary_10_1016_j_mehy_2020_109723
crossref_primary_10_1155_2020_8877862
crossref_primary_10_1016_j_sajb_2022_08_005
crossref_primary_10_1007_s00418_011_0869_0
crossref_primary_10_1016_j_jnutbio_2014_03_001
crossref_primary_10_3390_molecules25081996
crossref_primary_10_1016_j_scienta_2020_109365
crossref_primary_10_1158_1078_0432_CCR_10_1565
crossref_primary_10_1007_s10585_009_9250_2
crossref_primary_10_1016_j_febslet_2007_05_040
crossref_primary_10_4161_15384047_2014_955444
ContentType Journal Article
Copyright Copyright © 2007 Landes Bioscience 2007
Copyright_xml – notice: Copyright © 2007 Landes Bioscience 2007
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
DOI 10.4161/cbt.6.1.3548
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
DatabaseTitleList

MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Biology
EISSN 1555-8576
EndPage 61
ExternalDocumentID 10_4161_cbt_6_1_3548
17172819
10903548
Genre Research Paper
Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
00X
0R~
0VX
0YH
29B
30N
53G
5GY
6J9
AAAVI
AAJNR
ABBKH
ABCCY
ABEIZ
ABFIM
ABJVF
ACENM
ACGFO
ACGFS
ACTIO
ADBBV
ADCVX
AECIN
AEGYZ
AEISY
AENEX
AEXWM
AHDLD
AIJEM
AIRBT
ALMA_UNASSIGNED_HOLDINGS
ALQZU
AQRUH
AVBZW
AWQZV
BABNJ
BAWUL
BLEHA
C1A
CCCUG
DGEBU
DIK
DKSSO
E3Z
EBS
F5P
H13
IH2
KSSTO
KYCEM
M4Z
O9-
OK1
P2P
P6G
RPM
SJN
TFL
TFT
TFW
TR2
TTHFI
ZGOLN
-
0R
AGCAB
AIRXU
RNANH
ROSJB
RTWRZ
TQWBC
4.4
ACKZS
ADFZZ
AFPKN
AGYJP
AOIJS
AURDB
BFWEY
CGR
CUY
CVF
CWRZV
ECM
EIF
EJD
EMOBN
GROUPED_DOAJ
HYE
IPNFZ
LJTGL
NPM
PCLFJ
RIG
TDBHL
UDS
AAYXX
CITATION
ID FETCH-LOGICAL-c416t-df3a4c248555daa386eec890614c4d42be81cfc5953befa13686a2c14efe30583
ISSN 1538-4047
IngestDate Fri Aug 23 03:08:05 EDT 2024
Sat Sep 28 08:33:57 EDT 2024
Fri Jan 15 03:37:28 EST 2021
Tue Jul 04 18:15:19 EDT 2023
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c416t-df3a4c248555daa386eec890614c4d42be81cfc5953befa13686a2c14efe30583
OpenAccessLink https://www.tandfonline.com/doi/pdf/10.4161/cbt.6.1.3548?needAccess=true
PMID 17172819
PageCount 6
ParticipantIDs crossref_primary_10_4161_cbt_6_1_3548
landesbioscience_primary_cbt_article_3548
informaworld_taylorfrancis_310_4161_cbt_6_1_3548
pubmed_primary_17172819
PublicationCentury 2000
PublicationDate 1/1/2007
2007/01/01
2007-Jan
2007-01-00
PublicationDateYYYYMMDD 2007-01-01
PublicationDate_xml – month: 01
  year: 2007
  text: 1/1/2007
  day: 01
PublicationDecade 2000
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Cancer biology & therapy
PublicationTitleAlternate Cancer Biol Ther
PublicationYear 2007
Publisher Taylor & Francis
Publisher_xml – name: Taylor & Francis
References 17224638 - Cancer Biol Ther. 2007 Jan;6(1):62-3
References_xml
SSID ssj0027269
Score 2.0882928
Snippet We sought to investigate the apoptosis-inducing activities of quercetin, Siamois 1, and Siamois 2 against invasive estrogen-receptor negative MDA-MB 435 cells...
SourceID crossref
pubmed
landesbioscience
informaworld
SourceType Aggregation Database
Index Database
Publisher
StartPage 56
SubjectTerms Animals
Apoptosis
Binding
Biology
Bioscience
Breast Neoplasms - pathology
Calcium
Cancer
Cell
Cell Proliferation - drug effects
Cycle
Humans
Inhibitory Concentration 50
Landes
Mice
Mice, Nude
Organogenesis
Proteins
Quercetin - analogs & derivatives
Quercetin - pharmacology
Xenograft Model Antitumor Assays
Title Quercetin, Siamois 1 and siamois 2 induce apoptosis in human breast cancer MDA-MB-435 cells xenograft in vivo
URI https://www.tandfonline.com/doi/abs/10.4161/cbt.6.1.3548
http://www.landesbioscience.com/journals/cbt/article/3548/
https://www.ncbi.nlm.nih.gov/pubmed/17172819
Volume 6
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELbKIiE48H4sL_kAB1QS6sR5HZddYIXoSohdtLfIccZLD22qNl0hfgq_lpnYTdLSw8IlSixPXvPZnhnPg7FXIBOUUkfgaWS2J41QnspMgpeFSMKsVKBpR3d8Eh-fyc_n0flg8LvntbSqC1__2hlX8j9cxTbkK0XJ_gNn25tiA54jf_GIHMbjlXj8dUVuKS4NwLeJmlaT5VA0-wFLdxUMUeleUVTAvJrXFaUfmcxcZb6CHNJr8vvSsBiOjw688XsPBZshWfOXw58wI98t0xQRuJxcVn1B9tASrXM4EYDqzQQFR6B_LFdzZe3OU7Xo9vsrstdbnyCK-mo9b77D4qKy9foo9n_Sgu4LXFhofaJ46XLDVJH0TBXd7CpHNsWmD64tirw0skVg1lNy_Bfy7PQaxb2F2iZx314CSGFDvumi9mNf-GFkE3luZtreWgFbv0TUiIg-R-o8zkVO1NfY9QAnMZo9w9FJp8wHTbnE9pNsUAVRv-s_e0Pc2UiGe4vdId9V2gZ0aUthS7VpRJzTu-y20034gQXaPTaA2X12Y-y8Lx6waYu3t9yhjQuOd-cObTzgFm28RRs28AZt3KKNW7TxDm28QRtv0UYUhLaH7Ozjh9PDY8-V6_A0fnbtlSZUUjcp8qJSqTCNAQd6RiYHLUsZFJAKbXSURWEBRokwTmMVaCHBAK46afiI7c2qGTxhHHuHqdExZMbIUSFSLWUUQJKVAEqUcp-9Xv_VfG6zsuS7eLfPRv1fnteNFczYkjV5uJvkzTZb2kdQPzfYXd_Hll_dSyRU701kT6_4gs_YzW6gPGd79WIFL1DKrYuXDdz-AAy7qaI
link.rule.ids 315,783,787,27936,27937,60214,61003
linkProvider Taylor & Francis
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5BkYAeKM-2UMAHOCCREMfO61j60ALNSohWqrhYjjOWoqrJquutqv56PElK24ULHB3ZsuOZseflbwDeocy8lhphYDyxA2m5DnRhM9-seCaKWqOhiG45TSdH8utxcnyj1BelVZINbQegiP6sJuEmZzRJOOnjn0zlwjTkofDq9l24lxLuF73eiKbXtlbcV7Pr5VlGMhty3v8Yfes2uoVVugprlFpIUZoRVRKXNM_-Btpfg59Xax8ST07ChatCc7kE6_hfP_cYHo16KdseGOkJ3MH2Kdwvx8j7Mzj9vqAUGNe0H9mPRp92zZxx5mdh87EVM2_ee0ZhetbNXDf3n5qW9TUAWUWp744ZYrEzVu5uB-XnwKtQjOIGc3aBLWWJWUcjzpvz7jkc7e8d7kyCsVRDYPyiXVBboaXp4dGSWmuRp-iJXJC5aWQt4wpzbqxJikRUaDUXaZ7q2HCJFv2Jk4sXsNJ2LW4A871Fbk2KhbUyqnhupExizIoaUfNabsL7K5Kp2YDIobwlQ3un_N6pVHFFe7cJ0U16Ktd7QOxQrkSJvw_5sEzz31NQv1GYx77rAzNcLyKjWl-8ePnvE7-FB5PD8kAdfJl-ewUPB_8xuXm2YMWdLfC1V3xc9aZn8V-_GgDX
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB6VVqrgQFuebSn4AAckEuLYeR1L21Up7AoElcrJchxbilCTVddbof76ziRZ2i5c4JjIlh3PjP2N58sMwGsrM0SpkQ0MCjuQjutAFy7Dx5Jnoqi0NRTRHU_S41N5cpacrUC--BeGaJXkQ7s-UUS3V5NxTytHBk5w_L0pfZiGPBSItu_BGgKAiDRcRJMbVyvuitl15iwjmfWU9z963zmM7qQqfQAbxCykIM2QVNIuAc_uABptwI_F1Hveyc9w7svQXC1ldfyfb9uEhwMqZfu9Gm3Bim0ewfp4iLs_hvOvcyLA-Lp5x77V-rytZ4wzHITNhqeYoXOPasL0tJ36doav6oZ1FQBZScR3zwwp2AUbH-4H4w8BAihGUYMZ-2Ub4og5Tz0u68v2CZyOjr4fHAdDoYbA4KR9UDmhpemSoyWV1iJPLYq4IGfTyErGpc25cSYpElFap7lI81THhkvrLO43uXgKq03b2OfAsLXInUlt4ZyMSp4bKZPYZkVlreaV3IY3C4mpaZ-PQ6EfQ2uncO1UqriitduG6LY4le_uP1xfrESJv3d5uyzy30NQu8GUh7bPel24mURGlb54sfPvA7-C9S-HI_X54-TTLtzvL4_pjucFrPqLud1D1OPLl52CXwPGOv91
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Quercetin%2C+Siamois+1+and+siamois+2+induce+apoptosis+in+human+breast+cancer+MDA-MB-435+cells+xenograft+in+vivo&rft.jtitle=Cancer+biology+%26+therapy&rft.au=Dechsupa%2C+Samarn&rft.au=Kothan%2C+Suchart&rft.au=Vergote%2C+Jackie&rft.au=Leger%2C+Gerard&rft.date=2007-01-01&rft.issn=1538-4047&rft.eissn=1555-8576&rft.volume=6&rft.issue=1&rft.spage=56&rft.epage=61&rft_id=info:doi/10.4161%2Fcbt.6.1.3548&rft.externalDBID=n%2Fa&rft.externalDocID=10_4161_cbt_6_1_3548
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1538-4047&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1538-4047&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1538-4047&client=summon