LncRNA-ENST00000501520 promotes the proliferation of malignant-transformed BEAS-2B cells induced with coal tar pitch mediated by target genes.


Journal

Environmental toxicology
ISSN: 1522-7278
Titre abrégé: Environ Toxicol
Pays: United States
ID NLM: 100885357

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 11 02 2019
revised: 07 04 2019
accepted: 07 04 2019
pubmed: 30 4 2019
medline: 3 8 2019
entrez: 30 4 2019
Statut: ppublish

Résumé

As a human carcinogen, coal tar pitch (CTP) can significantly increase the risk of lung cancer. However, the mechanism underlying CTP-induced lung carcinogenesis has not been well understood. This study aims to explore the role of the LncRNA-ENST00000501520 in the proliferation of malignant-transformed human bronchial epithelial cells (BAES-2B) induced by CTP extract for the first time. BEAS-2B cells were stimulated with 2.4 μg/mL CTP extract, and then passaged for three times, which were named passage 1 and then passaged until passage 30 (named as CTP group). The ENST000001520 of cells in CTP group was interfered using siRNA. The results showed that ENST000001520 located in cell nucleus (>80%) had no or weak ability of protein encoding. After interference of ENST000001520, the migration and proliferation of cells in CTP group were inhibited, and the cell cycle was arrested in the G0/G1 phase; however, the apoptosis of cells in CTP group was promoted. The target genes (SKB1, CLTB, TAP2, PIPK2, and SOCS3) of ENST000001520 were screened out, and the mRNA and protein expression of SBK1 and SOCS3 was significantly decreased after ENST000001520 interference. SBK1 and SOCS3 may play a promoting role in occurrence and development of cancers. The study suggests that LncRNA-ENST00000501520 could promote the proliferation in malignant-transformed BEAS-2B cells induced with CTP extract which may be mediated by target genes. This study may provide a new target for prevention and treatment of lung cancer.

Identifiants

pubmed: 31033183
doi: 10.1002/tox.22759
doi:

Substances chimiques

RNA, Long Noncoding 0
Coal Tar 8007-45-2

Types de publication

Journal Article

Langues

eng

Pagination

869-877

Subventions

Organisme : National Natural Science Foundation of China
ID : 81172717
Organisme : National Natural Science Foundation of China
ID : 81402712
Organisme : Henan Department of Science and Technology, China
ID : 162102310319
Organisme : Medical Science Research Foundation of Henan Province
ID : 2018020477

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Zhongqiu Li (Z)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Yaping Zhang (Y)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Liya Meng (L)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Sa Yang (S)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Peng Zhang (P)

Department of Bone and soft tissue cancer, The Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), Zhengzhou, Henan, China.

Jiatong Zhang (J)

Department of Disease Control and Prevention, Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Chunyang Li (C)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Feifei Feng (F)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

Qiao Zhang (Q)

Department of Toxicology, College of Public Health, Zhengzhou University, Zhengzhou, Henan, China.

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Classifications MeSH