Estrogenic activities of sesame lignans and their metabolites : (Record no. 40329)

MARC details
000 -LEADER
fixed length control field 06034nas a2200469 a 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260818112538.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 130214s2011 th uu|m rtt 0| a1eng d
035 ## - SYSTEM CONTROL NUMBER
System control number .b12114972
099 #9 - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number AIT Diss. no.EV-11-04
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Prisna Pianjing
245 10 - TITLE STATEMENT
Title Estrogenic activities of sesame lignans and their metabolites :
Remainder of title interactive effect with cadmium in human breast cancer cell lines
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Pathum Thani, Thailand :
Name of publisher, distributor, etc. Asian Institute of Technology,
Date of publication, distribution, etc. 2011
300 ## - PHYSICAL DESCRIPTION
Extent 91 leaves :
Other physical details ill. (some col.)
490 1# - SERIES STATEMENT
Series statement Dissertation ;
Volume/sequential designation no. EV-11-04
500 ## - GENERAL NOTE
General note A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Environmental Engineering and Management Inter-University Program on Environmental Toxicology, Technology and Management, School of Environment, Resources and Development
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Ph.D.) - Asian Institute of Technology - Chulabhorn Research Institute - Mahidol University, 2011
520 ## - SUMMARY, ETC.
Summary, etc. The estrogenic activities of sesame lignans and their metabolites were investigated by using a viability assay and estrogen response elements (ERE) rep01ier system on the different levels of estrogen in cultured media. Hormone-dependent human breast cancer T47D cells and the cells stably transfected with ERE-luciferase reporter system T47DKBluc cells were utilized. Depending on levels of E2, sesame lignans and their metabolites exhibited different effects on the viability of T47D-KBluc cells. In the absence of estrogen, the trend of induction of cell growth was observed, whereas in the presence of estrogen, cytotoxic effect was evidenced. The ERE luciferase rep01ier assay in T47DKB1uc cells shows that, sesame lignans and their metabolites induced ERE activation. Among tested compounds, sesamol possessed the highest ERE activation prope1iy while ED showed no effect. All tested compounds exhibited lower levels of ERE activation than that of estradiol (E2) activation, suggesting that the tested compounds possess weak estrogenic effect. The antiestogen ICI 182 780 significantly decreased ERE activation induced by the te<ited compounds indicating the involvement of ER in their ERE activations. When 10 æM of tested compounds were co-incubated with various concentrations of E2 (10" 12-10"6 M), all tested compounds decreased the maximum responses of E2-ERE activations indicating that the tested compounds exhibit antiestrogenic effects in the presence of E2. Interestingly, tested compounds inhibited E2- ERE induction by a downward-shift of the E2-ERE dose-response curve. This was different from the inhibitory effects of tamoxifen and ICI 182 780 which showed the parallel-shift of E2-ERE dose-response curves without decreasing the maximum responses of E2-ERE induction. These results suggested that sesame lignans and their metabolites exhibited a non-competitive antagonistic property on E2-ERE activation. Real-time RTPCR studies showed that sesame lignans and their metabolites can induce estrogen targeted pS2 and progesterone receptor gene, suggesting their ERE induction abilities were functional. Cadmium at concentration 5 æM enhanced E2-ERE activation while sesamol, the most prominent ERE activator, could attenuate this response. When T47D cells were treated with cadmium, sesamol, or cadmium plus sesamol in the presence of E2, the results showed that cadmium increased expression of ERa while sesamol or sesamol plus cadmium decreased this expression, suggesting that sesamol may decrease cadmiuminduced estrogenic activity by modulating through ER. In particular, cadmium and sesamol induced alteration of ER expression in cytoplasm; whereas the expression of ERa in nucleus did not change when compared to control. Cadmium induced ERa expression in cytoplasm without the alteration of ERP expression when compared to control. Sesamol or sesamol plus cadmium decreased the expression of ERa while sesamol alone increased the expression of ERP in cytoplasm suggesting that in the presence of E2, sesamol preferentially interacted with ERa and ERP in cytoplasm. Sesamol may decrease cadmium-induced estrogenic activity by modulating ERa in cytoplasm. Fmihermore, these results indicate that sesame lignans and their metabolites possess estrogenic/antiestrogenic effect on ERE activation in human breast cancer cells in accordance with the E2 levels. In the presence of E2, sesamol, a metabolite form of sesamolin, may have the potential for prevention of cadmium- induced estrogenic effect in human breast cancer cells.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Seseme
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Estrogen
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Breast
General subdivision Cancer
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Jutamaad Satayavivad,
Relator term Chairperson
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Apinya Thiantanawat,
Relator term Co-Chairperson
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Preeda Pakpian,
Relator term Examination Committee
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nuchanart Rangkadilok,
Relator term Examination committee
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bung-om SripanidkulchaiIeExamination committee
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Chulabhorn Research Institute/Mahidol University/ AIT Fellowship (CRI-MU-AIT), Scholarship donor
810 2# - SERIES ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Asian Institute of Technology.
Title of a work Dissertation ;
Volume/sequential designation no. EV-11-04
856 ## - ELECTRONIC LOCATION AND ACCESS
Materials specified Full-Text
Uniform Resource Identifier <a href="http://203.159.5.9/ait-thesis/detail.php?q=B11290">http://203.159.5.9/ait-thesis/detail.php?q=B11290</a>
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998 ## - LOCAL CONTROL INFORMATION (RLIN)
Operator's initials, OID (RLIN) 0
Cataloger's initials, CIN (RLIN) 130214
First date, FD (RLIN) m
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Koha item type 20-AIT Publication
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      Available for Loans Asian Institute of Technology Library Asian Institute of Technology Library AIT Publications 18/08/2026 9.10   AIT Diss. no.EV-11-04 30050120553762 18/08/2026 1 18/08/2026 20-AIT Publication
      Available for Loans Asian Institute of Technology Library Asian Institute of Technology Library AIT Publications 18/08/2026 9.10   AIT Diss. no.EV-11-04 30050120553754 18/08/2026 2 18/08/2026 20-AIT Publication
      Available for Loans Asian Institute of Technology Library Asian Institute of Technology Library Archives 18/08/2026     AIT Diss. no.EV-11-04 30050160004056 18/08/2026   18/08/2026 40-Archives
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