Cargando…

Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis

LncRNA down syndrome cell adhesion molecule antisense 1 (DSCAM-AS1) plays an important role in tumor progression, but its function in pancreatic cancer is unknown. DSCAM-AS1 level was evaluated by in situ hybridization (ISH) assay and qRT-PCR. DSCAM-AS1 was knocked down in pancreatic cancer cells, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Xing, Wang, Zihe, Hou, Shengzhong, Yue, Chao, Li, ZhenLu, Hu, Weiming, Lu, Huimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973590/
https://www.ncbi.nlm.nih.gov/pubmed/35142595
http://dx.doi.org/10.1080/21655979.2021.2016326
_version_ 1784680070350110720
author Huang, Xing
Wang, Zihe
Hou, Shengzhong
Yue, Chao
Li, ZhenLu
Hu, Weiming
Lu, Huimin
author_facet Huang, Xing
Wang, Zihe
Hou, Shengzhong
Yue, Chao
Li, ZhenLu
Hu, Weiming
Lu, Huimin
author_sort Huang, Xing
collection PubMed
description LncRNA down syndrome cell adhesion molecule antisense 1 (DSCAM-AS1) plays an important role in tumor progression, but its function in pancreatic cancer is unknown. DSCAM-AS1 level was evaluated by in situ hybridization (ISH) assay and qRT-PCR. DSCAM-AS1 was knocked down in pancreatic cancer cells, and its impacts on cell proliferation, invasion, and migration were detected. The binding relationship among DSCAM-AS1, miR-136-5p, and pre-B-cell leukemia homeobox 3 (PBX3) was investigated by bioinformatic analysis and luciferase reporter assay. An in vivo animal model was constructed to determine the role of DSCAM-AS1 in tumor growth. Our results showed that DSCAM-AS1 was elevated in tumor tissues of pancreatic cancer patients and cell lines. DSCAM-AS1 knockdown efficiently inhibited PANC-1 cell proliferation, migration, and invasion and suppressed tumor growth. DSCAM-AS1 could promote PBX3 expression by sponging miR-136-5p, and its function in pancreatic cancer was partially mediated by the miR-136-5p/PBX3 axis. Overall, DSCAM-AS1 knockdown inhibits pancreatic cancer progression by modulating the miR-136-5p/PBX3 axis.
format Online
Article
Text
id pubmed-8973590
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-89735902022-04-02 Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis Huang, Xing Wang, Zihe Hou, Shengzhong Yue, Chao Li, ZhenLu Hu, Weiming Lu, Huimin Bioengineered Research Paper LncRNA down syndrome cell adhesion molecule antisense 1 (DSCAM-AS1) plays an important role in tumor progression, but its function in pancreatic cancer is unknown. DSCAM-AS1 level was evaluated by in situ hybridization (ISH) assay and qRT-PCR. DSCAM-AS1 was knocked down in pancreatic cancer cells, and its impacts on cell proliferation, invasion, and migration were detected. The binding relationship among DSCAM-AS1, miR-136-5p, and pre-B-cell leukemia homeobox 3 (PBX3) was investigated by bioinformatic analysis and luciferase reporter assay. An in vivo animal model was constructed to determine the role of DSCAM-AS1 in tumor growth. Our results showed that DSCAM-AS1 was elevated in tumor tissues of pancreatic cancer patients and cell lines. DSCAM-AS1 knockdown efficiently inhibited PANC-1 cell proliferation, migration, and invasion and suppressed tumor growth. DSCAM-AS1 could promote PBX3 expression by sponging miR-136-5p, and its function in pancreatic cancer was partially mediated by the miR-136-5p/PBX3 axis. Overall, DSCAM-AS1 knockdown inhibits pancreatic cancer progression by modulating the miR-136-5p/PBX3 axis. Taylor & Francis 2022-02-10 /pmc/articles/PMC8973590/ /pubmed/35142595 http://dx.doi.org/10.1080/21655979.2021.2016326 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Huang, Xing
Wang, Zihe
Hou, Shengzhong
Yue, Chao
Li, ZhenLu
Hu, Weiming
Lu, Huimin
Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title_full Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title_fullStr Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title_full_unstemmed Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title_short Long non-coding RNA DSCAM-AS1 promotes pancreatic cancer progression via regulating the miR-136-5p/PBX3 axis
title_sort long non-coding rna dscam-as1 promotes pancreatic cancer progression via regulating the mir-136-5p/pbx3 axis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973590/
https://www.ncbi.nlm.nih.gov/pubmed/35142595
http://dx.doi.org/10.1080/21655979.2021.2016326
work_keys_str_mv AT huangxing longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT wangzihe longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT houshengzhong longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT yuechao longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT lizhenlu longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT huweiming longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis
AT luhuimin longnoncodingrnadscamas1promotespancreaticcancerprogressionviaregulatingthemir1365ppbx3axis