اکثر مکاتبات کومش از طریق ایمیل سایت می باشد. لطفا Spam ایمیل خود را نیز چک نمایید.
   [Home ] [Archive]   [ فارسی ]  
:: ::
Main Menu
Home::
Journal Information::
Articles archive::
For Authors::
Subscription::
Contact us::
Site Facilities::
Webmail::
Editorial Board::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
:: Volume 17, Issue 4 (تابستان 1395: جلد 17 شماره (4) 1395) ::
Koomesh 1395, 17(4): 895-902 Back to browse issues page
Metabolome profile comparison of cisplatin sensitive and resistant in ovarian epithelial cells by magnetic resonance spectroscopy spectroscopy
Ziba Akbari , A. li Awsat Mellati , Amir Amanzadeh , Aboalfazl Nazarian , Zahra Zamani , Mohammad Arjmand
Abstract:   (5492 Views)
Introduction: Epithelial ovarian carcinoma is considered to be the most lethal gynecological malignancy in women and accounts for more than 85% of ovarian carcinomas. The chemotherapeutical treatment of choice is cisplatin. However, long-term use of this drug mostly results in drug resistance phenomenon. Metabolomics, is a highly resourceful technique, which acts promising in monitoring of tumor growth. Proton nuclear magnetic resonance spectroscopy (1H-NMR) is a non-invasive and high reproducible technique used in metabolomics. In the present investigation, we tried to find biochemical pathways and their metabolic alterations in epithelial cells of ovarian carcinoma and study the mechanism involved in cisplatin drug resistance. Materials and Methods: The cell lines A2780 and A2780CP were prepared. Methanol-chloroform-water extraction was performed.The hydrophilic layer were collected separately and cell1H-NMR spectroscopy were applied on a Bruker spectrometer operating at 400 MHz. After processing the data, outlier metabolites were identified and their biochemical pathways were worked out by Metaboanalyst and Human Metabolome Database. Results: In the present study, the main altered metabolites were fucose, sorbitol, mannitol, mannose, rhamnose, glycerol, galactonite, alpha lactose, myo-inositol and melibiose. The biochemical pathway enrichment analysis showed that galactose, fructose and mannose metabolism was the most prominent altered pathways. Conclusion: Our results disclose that cisplatin resistance results from alteration in carbohydrates metabolites and their pathways. However, further study is needed to confirm these findings
Keywords: Ovarian Carcinoma, Metabolomics, Cisplatin, Drug Resistance, 1H-NMR
Full-Text [PDF 725 kb]   (1223 Downloads)    
Type of Study: Research | Subject: General
Received: 2015/07/22 | Accepted: 2015/12/30 | Published: 2016/06/22
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Akbari Z, Awsat Mellati A L, Amanzadeh A, Nazarian A, Zamani Z, Arjmand M. Metabolome profile comparison of cisplatin sensitive and resistant in ovarian epithelial cells by magnetic resonance spectroscopy spectroscopy. Koomesh 1395; 17 (4) :895-902
URL: http://koomeshjournal.semums.ac.ir/article-1-2959-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 17, Issue 4 (تابستان 1395: جلد 17 شماره (4) 1395) Back to browse issues page
کومش Koomesh
Persian site map - English site map - Created in 0.05 seconds with 38 queries by YEKTAWEB 4645