Suitable reference gene for silencing methods using microRNA encapsulated nanoparticles chitosan for the ovarian cancer cell line

Wardana, Tirta and Ysrafil, Ysrafil and Sumadi, Firasti Agung Nugrahening and Martien, Ronny and Astuti, Indwiani and Mubarika, Sofia (2023) Suitable reference gene for silencing methods using microRNA encapsulated nanoparticles chitosan for the ovarian cancer cell line. Gene Reports, 33. ISSN 24520144

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Abstract

MicroRNAs (miRNAs) are key regulators of gene expression, and their accurate quantification is essential for elucidating miRNA functional roles. Quantitative reverse transcription PCR (qRT-PCR) is widely utilized for miRNA expression analyses, although appropriate data normalization is critical for generating reliable results. The present study aimed to identify a suitable reference gene for normalizing miRNA qRT-PCR data in the ovarian cancer cell line SKOV-3. SKOV-3 cells were treated with miRNA-loaded chitosan nanoparticles or left untreated as a control. Total RNA, including small RNAs, was extracted from SKOV-3 cells and assessed for quality. The expression stability of 15 candidate reference genes was evaluated by GeNorm analysis. miR-584-5p was identified as the most stably expressed reference gene. To validate miRNA profiling, miR-584-5p was used to normalize expression levels, revealing distinct patterns of differential miRNA expression. Our findings provide critical insights into aberrant miRNA expression in ovarian cancer cells and underscore proper normalization as essential for accurate quantification of miRNAs by qRT-PCR. © 2023 Elsevier Inc.

Item Type: Article
Additional Information: Cited by: 0
Uncontrolled Keywords: chitosan nanoparticle; complementary DNA; microRNA; microRNA 130b 3p; microRNA 140 3p; microRNA 143 3p; microRNA 191 5p; microRNA 194 5p; microRNA 25 3p; microRNA 28 3p; microRNA 28 5p; microRNA 421; microRNA 425 3p; microRNA 425 5p; microRNA 497 5p; microRNA 584 5p; microRNA 7c 5p; microRNA 7f 5p; unclassified drug; Article; cancer cell culture; cell encapsulation; controlled study; cycle threshold value; differential gene expression; DNA synthesis; down regulation; female; gene; gene expression profiling; gene silencing; genetic stability; human; human cell; nanoencapsulation; ovary cancer; real time polymerase chain reaction; real time reverse transcription polymerase chain reaction; reference gene; RNA extraction; RNA isolation; SK-OV-3 cell line; stable expression; upregulation
Subjects: R Medicine > RP Public Health and Nutrition
Divisions: Faculty of Pharmacy
Depositing User: Sri JUNANDI
Date Deposited: 11 Nov 2024 04:55
Last Modified: 11 Nov 2024 04:55
URI: https://ir.lib.ugm.ac.id/id/eprint/11198

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