A novel tRNA-derived fragment AS-tDR-007333 promotes the malignancy of NSCLC via the HSPB1/MED29 and ELK4/MED29 axes.


Journal

Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937

Informations de publication

Date de publication:
07 05 2022
Historique:
received: 23 12 2021
accepted: 21 04 2022
entrez: 7 5 2022
pubmed: 8 5 2022
medline: 11 5 2022
Statut: epublish

Résumé

Transfer RNA-derived fragments (tRFs) are a new class of small non-coding RNAs. Recent studies suggest that tRFs participate in some pathological processes. However, the biological functions and mechanisms of tRFs in non-small cell lung cancer (NSCLC) are largely unknown. Differentially expressed tRFs were identified by tRF and tiRNA sequencing using 9 pairs of pre- and post-operation plasma from patients with NSCLC. Quantitative real-time PCR (qRT-PCR) and fluorescence in situ hybridization (FISH) were used to determine the levels of tRF in tissues, plasma, and cells. Gain- and loss-of-function experiments were implemented to investigate the oncogenic effects of tRF on NSCLC cells in vitro and in vivo. Chromatin immunoprecipitation (ChIP), luciferase reporter, RNA pulldown, mass spectrum, RNA immunoprecipitation (RIP), Western blot, co-immunoprecipitation (Co-IP) assays, and rescue experiments were performed to explore the regulatory mechanisms of tRF in NSCLC. AS-tDR-007333 was an uncharacterized tRF and significantly up-regulated in NSCLC tissues, plasma, and cells. Clinically, AS-tDR-007333 overexpression could distinguish NSCLC patients from healthy controls and associated with poorer prognosis of NSCLC patients. Functionally, overexpression of AS-tDR-007333 enhanced proliferation and migration of NSCLC cells, whereas knockdown of AS-tDR-007333 resulted in opposite effects. Mechanistically, AS-tDR-007333 promoted the malignancy of NSCLC cells by activating MED29 through two distinct mechanisms. First, AS-tDR-007333 bound to and interacted with HSPB1, which activated MED29 expression by enhancing H3K4me1 and H3K27ac in MED29 promoter. Second, AS-tDR-007333 stimulated the expression of transcription factor ELK4, which bound to MED29 promoter and increased its transcription. Therapeutically, inhibition of AS-tDR-007333 suppressed NSCLC cell growth in vivo. Our study identifies a new oncogenic tRF and uncovers a novel mechanism that AS-tDR-007333 promotes NSCLC malignancy through the HSPB1-MED29 and ELK4-MED29 axes. AS-tDR-007333 is a potential diagnostic or prognostic marker and therapeutic target for NSCLC.

Sections du résumé

BACKGROUND
Transfer RNA-derived fragments (tRFs) are a new class of small non-coding RNAs. Recent studies suggest that tRFs participate in some pathological processes. However, the biological functions and mechanisms of tRFs in non-small cell lung cancer (NSCLC) are largely unknown.
METHODS
Differentially expressed tRFs were identified by tRF and tiRNA sequencing using 9 pairs of pre- and post-operation plasma from patients with NSCLC. Quantitative real-time PCR (qRT-PCR) and fluorescence in situ hybridization (FISH) were used to determine the levels of tRF in tissues, plasma, and cells. Gain- and loss-of-function experiments were implemented to investigate the oncogenic effects of tRF on NSCLC cells in vitro and in vivo. Chromatin immunoprecipitation (ChIP), luciferase reporter, RNA pulldown, mass spectrum, RNA immunoprecipitation (RIP), Western blot, co-immunoprecipitation (Co-IP) assays, and rescue experiments were performed to explore the regulatory mechanisms of tRF in NSCLC.
RESULTS
AS-tDR-007333 was an uncharacterized tRF and significantly up-regulated in NSCLC tissues, plasma, and cells. Clinically, AS-tDR-007333 overexpression could distinguish NSCLC patients from healthy controls and associated with poorer prognosis of NSCLC patients. Functionally, overexpression of AS-tDR-007333 enhanced proliferation and migration of NSCLC cells, whereas knockdown of AS-tDR-007333 resulted in opposite effects. Mechanistically, AS-tDR-007333 promoted the malignancy of NSCLC cells by activating MED29 through two distinct mechanisms. First, AS-tDR-007333 bound to and interacted with HSPB1, which activated MED29 expression by enhancing H3K4me1 and H3K27ac in MED29 promoter. Second, AS-tDR-007333 stimulated the expression of transcription factor ELK4, which bound to MED29 promoter and increased its transcription. Therapeutically, inhibition of AS-tDR-007333 suppressed NSCLC cell growth in vivo.
CONCLUSIONS
Our study identifies a new oncogenic tRF and uncovers a novel mechanism that AS-tDR-007333 promotes NSCLC malignancy through the HSPB1-MED29 and ELK4-MED29 axes. AS-tDR-007333 is a potential diagnostic or prognostic marker and therapeutic target for NSCLC.

Identifiants

pubmed: 35526007
doi: 10.1186/s13045-022-01270-y
pii: 10.1186/s13045-022-01270-y
pmc: PMC9077895
doi:

Substances chimiques

ELK4 protein, human 0
HSPB1 protein, human 0
Heat-Shock Proteins 0
Molecular Chaperones 0
ets-Domain Protein Elk-4 146481-62-1
RNA, Transfer 9014-25-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

53

Subventions

Organisme : National Natural Science Foundation of China
ID : 41977372
Organisme : National Natural Science Foundation of China
ID : 81972003
Organisme : Science and Technology Program of Guangdong Province
ID : 2017B 030301016
Organisme : Natural Science Foundation of Guangdong Province
ID : 2019A1515010210
Organisme : Natural Science Foundation of Guangdong Province
ID : 2021A1515011046
Organisme : Natural Science Foundation of Guangdong Province
ID : 2021A1515012144
Organisme : Shenzhen Science and Technology Innovation Commission
ID : JCYJ20180507182427559
Organisme : Shenzhen Science and Technology Innovation Commission
ID : JCYJ20170818100842319
Organisme : Guangdong Medical Research Foundation
ID : A2018312
Organisme : Shenzhen University
ID : 86000000210

Informations de copyright

© 2022. The Author(s).

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Auteurs

Wenhan Yang (W)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Kaiping Gao (K)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Youhui Qian (Y)

Department of Thoracic Surgery, The First Affiliated Hospital of Shenzhen University, 3002 West Shungang Road, Shenzhen, 518035, China.

Yongyi Huang (Y)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Qin Xiang (Q)

Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Cheng Chen (C)

Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Qianqian Chen (Q)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Yiling Wang (Y)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Fuyuan Fang (F)

Department of Thoracic Surgery, The First Affiliated Hospital of Shenzhen University, 3002 West Shungang Road, Shenzhen, 518035, China.

Qihan He (Q)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Siqi Chen (S)

Department of Thoracic Surgery, The First Affiliated Hospital of Shenzhen University, 3002 West Shungang Road, Shenzhen, 518035, China.

Juan Xiong (J)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China.

Yangchao Chen (Y)

Faculty of Medicine, The Chinese University of Hong Kong, Rm508A, Lo Kwee-Seong Integrated Biomedical Sciences Bldg, Shatin, NT, Hong Kong, China.

Ni Xie (N)

Department of Thoracic Surgery, The First Affiliated Hospital of Shenzhen University, 3002 West Shungang Road, Shenzhen, 518035, China. xn100@szu.edu.cn.

Duo Zheng (D)

Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China. dzheng@szu.edu.cn.

Rihong Zhai (R)

School of Public Health, Shenzhen University Health Science Center, 1066 Xueyuan Ave., Shenzhen, 518055, China. rzhai@szu.edu.cn.
Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, International Cancer Center, Shenzhen University Health Science Center, Shenzhen, China. rzhai@szu.edu.cn.
Department of Thoracic Surgery, Shenzhen University General Hospital, 1098 Xueyuan Ave., Shenzhen, 518055, China. rzhai@szu.edu.cn.

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Classifications MeSH