ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells

Abstract Long non-coding RNAs (lncRNAs) play important roles in many pathophysiological processes, including cancer progression. Namely, lncRNA Receptor-tyrosine-kinase-like orphan receptor-1 antisense 1 (ROR1-AS1) is crucial for cancer occurrence and progression in organs such as the liver or bladd...

Full description

Bibliographic Details
Main Authors: Xueliang Li, Zhaowei Sun, Li Wang, Qinlei Wang, Maobing Wang, Jingyun Guo, Haoran Li, MenShou Chen, Guanghua Cao, Yanan Yu, Haochen Zhong, Hao Zou, Kai Ma, Bingyuan Zhang, Guolei Wang, Yujie Feng
Format: Article
Language:English
Published: BMC 2023-09-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-023-11412-1
_version_ 1797559147717197824
author Xueliang Li
Zhaowei Sun
Li Wang
Qinlei Wang
Maobing Wang
Jingyun Guo
Haoran Li
MenShou Chen
Guanghua Cao
Yanan Yu
Haochen Zhong
Hao Zou
Kai Ma
Bingyuan Zhang
Guolei Wang
Yujie Feng
author_facet Xueliang Li
Zhaowei Sun
Li Wang
Qinlei Wang
Maobing Wang
Jingyun Guo
Haoran Li
MenShou Chen
Guanghua Cao
Yanan Yu
Haochen Zhong
Hao Zou
Kai Ma
Bingyuan Zhang
Guolei Wang
Yujie Feng
author_sort Xueliang Li
collection DOAJ
description Abstract Long non-coding RNAs (lncRNAs) play important roles in many pathophysiological processes, including cancer progression. Namely, lncRNA Receptor-tyrosine-kinase-like orphan receptor-1 antisense 1 (ROR1-AS1) is crucial for cancer occurrence and progression in organs such as the liver or bladder. However, its expression and role in cholangiocarcinoma (CCA) have not been thoroughly explored. Firstly, we assessed cell viability, proliferation, invasion, and migration using three cell lines (HuCCT-1, QBC399, and RBE) to explore the biological characteristics of ROR1-AS1 in CCA. Secondly, to determine the in vivo effect of ROR1-AS1 on tumor growth, ROR1-AS1 knockdown (KD) HuCCT-1 cells were subcutaneously injected into nude mice to evaluate tumor growth. Finally, we conducted a bioinformatic analysis to confirm the role of ROR1-AS1 in the prognosis and immunity of CCA. In this study, we found that lncRNA ROR1-AS1 was increased in CCA samples and patients with higher ROR1-AS1 expression had a shorter overall survival period. siRNA-mediated KD of ROR1-AS1 significantly reduced cell proliferation and inhibited the migration of CCA cells. In addition, ROR1-AS1 KD HuCCT-1 cells injected into nude mice grew slower than normal CCA cells. In summary, our results show that ROR1-AS1 can promote CCA progression and might serve as a new target for diagnosis and treatment of CCA.
first_indexed 2024-03-10T17:41:20Z
format Article
id doaj.art-f547cd5583564412bc18ba29d717b805
institution Directory Open Access Journal
issn 1471-2407
language English
last_indexed 2024-03-10T17:41:20Z
publishDate 2023-09-01
publisher BMC
record_format Article
series BMC Cancer
spelling doaj.art-f547cd5583564412bc18ba29d717b8052023-11-20T09:43:10ZengBMCBMC Cancer1471-24072023-09-0123111210.1186/s12885-023-11412-1ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cellsXueliang Li0Zhaowei Sun1Li Wang2Qinlei Wang3Maobing Wang4Jingyun Guo5Haoran Li6MenShou Chen7Guanghua Cao8Yanan Yu9Haochen Zhong10Hao Zou11Kai Ma12Bingyuan Zhang13Guolei Wang14Yujie Feng15Department of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of operating theater, the Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, HuiKang Hospital of the Affiliated Hospital of Qingdao University of QingdaoDepartment of Internal Medicine-Cardiovascular, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, HuiKang Hospital of the Affiliated Hospital of Qingdao University of QingdaoDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityDepartment of Hepatobiliary and Pancreatic Surgery, The Affiliated Hospital of Qingdao UniversityAbstract Long non-coding RNAs (lncRNAs) play important roles in many pathophysiological processes, including cancer progression. Namely, lncRNA Receptor-tyrosine-kinase-like orphan receptor-1 antisense 1 (ROR1-AS1) is crucial for cancer occurrence and progression in organs such as the liver or bladder. However, its expression and role in cholangiocarcinoma (CCA) have not been thoroughly explored. Firstly, we assessed cell viability, proliferation, invasion, and migration using three cell lines (HuCCT-1, QBC399, and RBE) to explore the biological characteristics of ROR1-AS1 in CCA. Secondly, to determine the in vivo effect of ROR1-AS1 on tumor growth, ROR1-AS1 knockdown (KD) HuCCT-1 cells were subcutaneously injected into nude mice to evaluate tumor growth. Finally, we conducted a bioinformatic analysis to confirm the role of ROR1-AS1 in the prognosis and immunity of CCA. In this study, we found that lncRNA ROR1-AS1 was increased in CCA samples and patients with higher ROR1-AS1 expression had a shorter overall survival period. siRNA-mediated KD of ROR1-AS1 significantly reduced cell proliferation and inhibited the migration of CCA cells. In addition, ROR1-AS1 KD HuCCT-1 cells injected into nude mice grew slower than normal CCA cells. In summary, our results show that ROR1-AS1 can promote CCA progression and might serve as a new target for diagnosis and treatment of CCA.https://doi.org/10.1186/s12885-023-11412-1CholangiocarcinomaImmune infiltrationEnrichment analysisPrognosisTumor proliferationMigration and invasion
spellingShingle Xueliang Li
Zhaowei Sun
Li Wang
Qinlei Wang
Maobing Wang
Jingyun Guo
Haoran Li
MenShou Chen
Guanghua Cao
Yanan Yu
Haochen Zhong
Hao Zou
Kai Ma
Bingyuan Zhang
Guolei Wang
Yujie Feng
ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
BMC Cancer
Cholangiocarcinoma
Immune infiltration
Enrichment analysis
Prognosis
Tumor proliferation
Migration and invasion
title ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
title_full ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
title_fullStr ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
title_full_unstemmed ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
title_short ROR1-AS1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
title_sort ror1 as1 might promote in vivo and in vitro proliferation and invasion of cholangiocarcinoma cells
topic Cholangiocarcinoma
Immune infiltration
Enrichment analysis
Prognosis
Tumor proliferation
Migration and invasion
url https://doi.org/10.1186/s12885-023-11412-1
work_keys_str_mv AT xueliangli ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT zhaoweisun ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT liwang ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT qinleiwang ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT maobingwang ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT jingyunguo ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT haoranli ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT menshouchen ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT guanghuacao ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT yananyu ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT haochenzhong ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT haozou ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT kaima ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT bingyuanzhang ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT guoleiwang ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells
AT yujiefeng ror1as1mightpromoteinvivoandinvitroproliferationandinvasionofcholangiocarcinomacells