Regulation of Stemness, Metastasis and Drug Resistance By MicroRNAs in Gastric cancer

Publish Year: 1395
نوع سند: مقاله کنفرانسی
زبان: English
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IPMCMED01_030

تاریخ نمایه سازی: 23 آذر 1397

Abstract:

Objective or background: Cancer stem cells (CSCs) have a significant role in spread out and cancer metastasis as well as resistance to conventional therapy. MiRNA is one of the regulatory elements which can regulate metastasis, stemness and drug-resistance properties simultaneously. Therefore, in this study, by using literature learning and data mining, 30 miRNAs obtained that are able to regulate any third of these properties in gastric cancer. Materials & methods: published articles from PubMed online database were obtained using search strategy:((stem cell OR sphere OR side population) AND (miRNA OR microRNA) AND (profiling)). 138 studies were collected from mentioned search strategy and after removing duplicates, non-full-text and non-related topics and abstracts, 21 studies were selected (figure 1). Figure 1. Flowchart of study selection.A total of 200 miRNAs which regulate stemness, were observed in 21 studies.For extracting miRNAs that regulate metastasis, we used the miRCancer database. Then we observed 76 miRNAs are common between metastasis and stemness.And for the drug resistance feature, we used the PUBMED database and analyzed 30 common miRNAs in these three properties. (figure 2).2. Venn diagram shows the Number of common miRNAs.RESULTS: Based on different sets of data, 30 miRNAs including: hsa-miR-197, hsa-let-7f, hsa-miR-34a, hsa-miR-21 , hsa-miR-7g , hsa-miR-107, hsa- miR-7d , hsa-miR-149 , hsa-miR-375 , hsa-miR-30a , hsa-miR-103a , hsa-miR-224 , hsa-miR-129-1, hsa-miR-197, hsa-miR-125b, hsa-miR-24, hsa-miR-20a, hsa-miR-223, hsa-miR-129-2, hsa-miR-149, hsa-miR-23b, hsa-miR-27a, hsa-miR-338, hsa-miR-181b, hsa-miR-27b, hsa-miR-140, hsa- miR-19b, hsa-miR-92, hsa-miR-524 and hsa-miR-106b play a role in resistance to conventional therapy, stemness, metastasis in gastric cancer.

Authors

Mahnaz Azimi

Department of Genetics, University of Science and Culture, ACECR, Tehran, Iran

Marzieh Ebrahimi

Department of Stem Cells and Developmental Biology at Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran

Mehdi Tootoonchi

Department of Genetics, Reproductive Biomedical Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran

Parisa Sahranavard

Department of Genetics, Reproductive Biomedical Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran