hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells

Gastric cancer (GC) is one of the most common cancers worldwide and is thus a global cancer burden. Here, we focused on a novel circular RNA hsa_circ_0092306 and explored the potential molecular mechanism to provide a new target for and novel insights into GC treatment. The GEO microarray was mined ...

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Main Authors: Zihao Chen, Hongping Ju, Ting Zhao, Shan Yu, Ping Li, Jing Jia, Nan Li, Xiaojie Jing, Bibo Tan, Yong Li
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Molecular Therapy: Nucleic Acids
Online Access:http://www.sciencedirect.com/science/article/pii/S2162253119302252
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spelling doaj-9d9fdf73bb3743c4b585c39ec8dee9cd2020-11-25T02:17:53ZengElsevierMolecular Therapy: Nucleic Acids2162-25312019-12-0118617626hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 CellsZihao Chen0Hongping Ju1Ting Zhao2Shan Yu3Ping Li4Jing Jia5Nan Li6Xiaojie Jing7Bibo Tan8Yong Li9Graduate School of Hebei Medical University, Shijiazhuang 050017, Hebei, China; The Third Department of Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, ChinaSchool of Medicine, Kunming University, Kunming 650214, Yunnan, China; The Respiratory System Disease Prevention and Control of Public Service Platform of Science and Technology in Yunnan Province, Kunming 650214, Yunnan, China; Corresponding author: Hongping Ju, School of Medicine, Kunming University, No. 2 Puxin Road, Kunming 650214, Yunnan, China.Graduate School of Hebei Medical University, Shijiazhuang 050017, Hebei, ChinaSchool of Medicine, Kunming University, Kunming 650214, Yunnan, ChinaSchool of Medicine, Kunming University, Kunming 650214, Yunnan, ChinaSchool of Medicine, Kunming University, Kunming 650214, Yunnan, ChinaSchool of Medicine, Kunming University, Kunming 650214, Yunnan, ChinaDepartment of Medicine, The People’s Hospital of Economic and Technological Development Zone, Kunming 650217, Yunnan, ChinaThe Third Department of Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, ChinaThe Third Department of Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China; Corresponding author: Yong Li, The Third Department of Surgery, The Fourth Hospital of Hebei Medical University, No. 12 Jiankang Road, Shijiazhuang 050011, Hebei, China.Gastric cancer (GC) is one of the most common cancers worldwide and is thus a global cancer burden. Here, we focused on a novel circular RNA hsa_circ_0092306 and explored the potential molecular mechanism to provide a new target for and novel insights into GC treatment. The GEO microarray was mined and analyzed with R software. Sanger sequencing and RNase R assay were applied to verify the identification of hsa_circ_0092306. Quantitative real-time PCR and western blot were performed to measure the mRNA and protein levels. Pull-down and luciferase reporter assays were conducted to confirm the target relationships. Annexin V-PI apoptosis flow cytometry, 3-(4,5Dimethylthiazol- yl)-2,5Dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide (MTT), wound healing, and Transwell assays were applied to detect cell apoptosis, viability, migration, and invasion in MKN-45 cells, respectively. A xenograft in vivo experiment was conducted to confirm the cell experiment results. hsa_circ_0092306 was upregulated in GC tissues and GC cells, and promoted GC development in MKN-45 cells. hsa_circ_0092306 inhibited tumor suppressor miR-197-3p expression but promoted tumor promotor protein kinase C beta (PRKCB) expression in MKN-45 cells. hsa_circ_0092306 and PRKCB had a common target (miR-197-3p) and were negatively related to miR-197-3p expression. hsa_circ_0092306 promoted the development of GC by regulating the pathway of miR-197-3p/PRKCB in MKN-45 cells. Keywords: gastric cancer, circular RNA, hsa_circ_0092306, miR-197-3p, PRKCB, protein kinase C betahttp://www.sciencedirect.com/science/article/pii/S2162253119302252
collection DOAJ
language English
format Article
sources DOAJ
author Zihao Chen
Hongping Ju
Ting Zhao
Shan Yu
Ping Li
Jing Jia
Nan Li
Xiaojie Jing
Bibo Tan
Yong Li
spellingShingle Zihao Chen
Hongping Ju
Ting Zhao
Shan Yu
Ping Li
Jing Jia
Nan Li
Xiaojie Jing
Bibo Tan
Yong Li
hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
Molecular Therapy: Nucleic Acids
author_facet Zihao Chen
Hongping Ju
Ting Zhao
Shan Yu
Ping Li
Jing Jia
Nan Li
Xiaojie Jing
Bibo Tan
Yong Li
author_sort Zihao Chen
title hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
title_short hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
title_full hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
title_fullStr hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
title_full_unstemmed hsa_circ_0092306 Targeting miR-197-3p Promotes Gastric Cancer Development by Regulating PRKCB in MKN-45 Cells
title_sort hsa_circ_0092306 targeting mir-197-3p promotes gastric cancer development by regulating prkcb in mkn-45 cells
publisher Elsevier
series Molecular Therapy: Nucleic Acids
issn 2162-2531
publishDate 2019-12-01
description Gastric cancer (GC) is one of the most common cancers worldwide and is thus a global cancer burden. Here, we focused on a novel circular RNA hsa_circ_0092306 and explored the potential molecular mechanism to provide a new target for and novel insights into GC treatment. The GEO microarray was mined and analyzed with R software. Sanger sequencing and RNase R assay were applied to verify the identification of hsa_circ_0092306. Quantitative real-time PCR and western blot were performed to measure the mRNA and protein levels. Pull-down and luciferase reporter assays were conducted to confirm the target relationships. Annexin V-PI apoptosis flow cytometry, 3-(4,5Dimethylthiazol- yl)-2,5Dimethylthiazol-2-yl)-2,5diphenyltetrazolium bromide (MTT), wound healing, and Transwell assays were applied to detect cell apoptosis, viability, migration, and invasion in MKN-45 cells, respectively. A xenograft in vivo experiment was conducted to confirm the cell experiment results. hsa_circ_0092306 was upregulated in GC tissues and GC cells, and promoted GC development in MKN-45 cells. hsa_circ_0092306 inhibited tumor suppressor miR-197-3p expression but promoted tumor promotor protein kinase C beta (PRKCB) expression in MKN-45 cells. hsa_circ_0092306 and PRKCB had a common target (miR-197-3p) and were negatively related to miR-197-3p expression. hsa_circ_0092306 promoted the development of GC by regulating the pathway of miR-197-3p/PRKCB in MKN-45 cells. Keywords: gastric cancer, circular RNA, hsa_circ_0092306, miR-197-3p, PRKCB, protein kinase C beta
url http://www.sciencedirect.com/science/article/pii/S2162253119302252
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