Carthamus tinctorius l. Inhibits proliferation of lung cancer A549 cells and tender’s mitochondrial protection (Record no. 17338)

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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17617
Author Dailah, Hamad Ghaleb
245 ## - TITLE STATEMENT
Title Carthamus tinctorius l. Inhibits proliferation of lung cancer A549 cells and tender’s mitochondrial protection
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(3), Jul-Sep
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 789-794p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: Plant-based products are well-known as long-lasting chemo preventive and<br/>chemotherapeutic medicines against cancer. Objectives: The purpose of this research<br/>is to identify out how safflower extract affects A549 cells. Materials and Methods:<br/>The antiproliferative activity was determined using the Trypan blue assay, while the<br/>cytotoxicity was determined using the MTT assay. The ethidium bromide/acridine<br/>orange (AO/EB) dual staining method was used to observe the apoptotic inducing effect<br/>and the morphological assessment of A549 cells using phase contrast microscopy<br/>was studied to discern the nuclear changes if any on treatment with safflower.<br/>The mitochondrial membrane potential was studied using a cationic lipophilic dye<br/>rhodamine 123 under a confocal microscope, and oxidative stress was assessed using<br/>2’,7’-dichlorodihydrofluorescein diacetate (DCFH-DA) labelling. Results: The trypan blue<br/>assay speculated that there was a decrease in cell viability at highest concentration and<br/>that the effect was dose dependent. The MTT assay revealed that cytotoxicity increases<br/>in cells treated with higher concentration. The LC50 range of the sample was found at<br/>250 μg/ml concentration at 52.2%, whereas the viability of the cell declined to 28.19%<br/>at 350μg/ml concentration. The morphological features like shrinkage, detachment,<br/>membrane blebbing, and distorted shape were observed on safflower treated A549 cells<br/>that supports the antiproliferative activity. The ethidium bromide and acridine orange<br/>staining substantiates that safflower extract induces apoptosis wherein the untreated<br/>A549 cells showed green fluorescence with intact nuclear morphology and cells treated<br/>with safflower extract (200 μg and 250 μg/ml), showed apoptotic bodies, clearly<br/>validating the apoptosis inducing effect by safflower on A549 cells. Also, the safflower<br/>extract protects the mitochondria by decreasing the oxidative stress and by altering the<br/>mitochondrial membrane potential. Conclusion: Thus, it is found that safflower extract<br/>exerts its antiproliferative activity by inducing apoptosis and protects mitochondria by<br/>combating oxidative stress.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
Title Indian journal of pharmaceutical education and research
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-3-789.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 26/08/2022   2022-1389 26/08/2022 26/08/2022 Articles Abstract Database
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