Curcumin induces human glioma cell apoptosis by promoting reactive oxygen species production (Record no. 16931)

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control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220628095432.0
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fixed length control field 220628b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 16858
Author Zhou, Yu
245 ## - TITLE STATEMENT
Title Curcumin induces human glioma cell apoptosis by promoting reactive oxygen species production
250 ## - EDITION STATEMENT
Volume, Issue number Vol.83(4), Jul-Aug
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Journal of Pharmaceutical Science
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 714-722p.
520 ## - SUMMARY, ETC.
Summary, etc. Malignant glioma by surgery is difficult to completely remove, the recurrence rate is high, the survival
period is short and the prognosis is poor, which poses a great threat to human health. This article mainly
studies the related process that curcumin induces human glioma cell apoptosis by promoting reactive
oxygen species production. In the experiment, glioma cells were processed and Uppsala 87 malignant
glioma cells of human were cultured in vitro. 3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium
bromide assay was used to detect the effect of curcumin on the proliferation of Uppsala 87 malignant
glioma cells. The cells in each reagent group and control group treated with curcumin were treated with
3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide colorimetric treatment at 24 h. Use flow
cytometry to detect cell apoptosis. Cellular immunofluorescence was used to detect the effect of oxidase
inhibitors on nuclear factor activation. Experimental data showed that the apoptotic rate of 0, 2.5,
5 mg/l, diallyl disulphide treatment groups were 12.3 %, 19.75 % and 26.44 %, respectively, indicating
that diallyl disulphide caused an increase in the apoptotic rate of human promyelocytic leukemia cell line
cells and the difference was statistically significant (p<0.05). The results show that curcumin can inhibit
the proliferation of Uppsala 87 malignant glioma cells cultured in vitro, induce the differential expression
of apoptosis-related genes and thus have a significant effect of promoting cell apoptosiss.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 16859
Co-Author Liu, Li
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical sciences
Place, publisher, and date of publication New Delhi
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/curcumin-induces-human-glioma-cell-apoptosis-by-promoting-reactive-oxygen-species-production.pdf
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942 ## - ADDED ENTRY ELEMENTS (KOHA)
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          School of Pharmacy School of Pharmacy Archieval Section 2022-06-28 2022-0920 2022-06-28 2022-06-28 Articles Abstract Database
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