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pmid:31258730

Small Nucleolar RNA 71A Promotes Lung Cancer Cell Proliferation, Migration and Invasion via MAPK/ERK Pathway.

Guiliang Tang · Zihang Zeng · Wenjie Sun · Shuying Li · Chengcheng You · Fang Tang · Shan Peng · Shijing Ma · Yuan Luo · Jieyu Xu · Xiaoli Tian · Nannan Zhang · Yan Gong · Conghua Xie

Journal of Cancer · 2019 doi:10.7150/jca.31077

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:31258730
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science-record
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title
Small Nucleolar RNA 71A Promotes Lung Cancer Cell Proliferation, Migration and Invasion via MAPK/ERK Pathway.
doi
10.7150/jca.31077
pmid
31258730
authors array · 14 items
[0]
Guiliang Tang
[1]
Zihang Zeng
[2]
Wenjie Sun
[3]
Shuying Li
[4]
Chengcheng You
[5]
Fang Tang
[6]
Shan Peng
[7]
Shijing Ma
[8]
Yuan Luo
[9]
Jieyu Xu
[10]
Xiaoli Tian
[11]
Nannan Zhang
[12]
Yan Gong
[13]
Conghua Xie
journal
Journal of Cancer
year
2019
abstract
Objective: Increasing evidence suggested that dysregulated small nucleolar RNAs (snoRNAs) were involved in tumor development. The roles of snoRNA 71A (SNORA71A) in the progression of non-small cell lung cancer (NSCLC) remained unclear. Methods: Dataset GSE19188 from Gene Expression Omnibus (GEO) database was downloaded to detect the expression levels of SNORA71A in NSCLC tissues. The biological significance of SNORA71A was explored by loss-of-function analysis both in vitro and in vivo. Results: SNORA71A was overexpressed in NSCLC tissues compared with normal tissues, and upregulated SNORA71A was significantly associated with worse survival of NSCLC patients. Knockdown of SNORA71A suppressed proliferation of both A549 and PC9 cells, and induced G0/G1 phase arrest. Knockdown of SNORA71A also suppressed xenograft tumor growth in mice. In addition, knockdown of SNORA71A inhibited cell invasion and migration and suppressed epithelial-mesenchymal transition. Furthermore, downregulated SNORA71A decreased the phosphorylation of MEK and ERK1/2 in the MAPK/ERK signal pathway. Conclusion: SNORA71A functions as an oncogene in NSCLC and may serve as a therapeutic target and promising prognostic biomarker of NSCLC.
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Expression data for early stage NSCLC
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[0]
asset:data:geo:GSE19188 licence not read
[1]
asset:data:geo:GSE19188 not downloaded
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execution.not_run
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method.student_t
[4]
review.human_critique
[5]
review.independent_reader
[6]
review.machine_critique
[7]
step:run_analysis blocked on method:student_t
assays array · 4 items
[0] object · 11 fields
role
data_generation
definition_id
animal_model
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 4 items
[0]
loss-of-function analysis both in vitro and in vivo. Results: SNORA71A was overexpressed in NSCL
[1]
RA71A also suppressed xenograft tumor growth in mice. In addition, knockdown of SNORA71A inhibite
[2]
h × width × width × 0.5). After 8 weeks, the mice were anesthetized with pentobarbital (Sigma Chemi
[3]
S Lumina XRMS Series III (PerkinElmer, USA). Mice were then sacrificed and tumors were exercised. A
order_basis
paper_text_order:549
id
assay:1
[1] object · 11 fields
role
data_generation
definition_id
transfection
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 4 items
[0]
iated with worse survival of NSCLC patients. Knockdown of SNORA71A suppressed proliferation of both
[1]
d PC9 cells, and induced G0/G1 phase arrest. Knockdown of SNORA71A also suppressed xenograft tumor
[2]
xenograft tumor growth in mice. In addition, knockdown of SNORA71A inhibited cell invasion and migr
[3]
ries (Beijing, China). A549-LV-NC or A549-LV-siRNA cells (4 × 106 per 100 μl) were injected sub
order_basis
paper_text_order:733
id
assay:2
[2] object · 11 fields
role
data_generation
definition_id
cell_culture
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.99
evidence array · 4 items
[0]
of SNORA71A suppressed proliferation of both A549 and PC9 cells, and induced G0/G1 phase arres
[1]
nces (Shanghai, China). All these cells were cultured in RPMI-1640 medium (Hyclone Ltd., USA) supplem
[2]
methods Cell culture Lung cancer cell lines (A549, PC9, NCI-H1299, NCI-H1975, H292, H460, H661
[3]
e Vital River Laboratories (Beijing, China). A549-LV-NC or A549-LV-siRNA cells (4 × 106 per 10
order_basis
paper_text_order:788
id
assay:3
[3] object · 11 fields
role
analysis
definition_id
group_comparison
definition_version
f2132e96ae6c7a4e
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Unpaired 2 tail student's t-test was used for comparison between groups.
order_basis
consumes_earlier_output
id
assay:4
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31258730", "kind": "science-record", "revision": 8, "content_hash": "sha256:be1599b602e1ff762a509798f95b5738ebed32474ba7a7f81366b004e33e6e01", "created_at": "2026-11-01T15:40:46Z", "updated_at": "2026-11-01T22:00:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Small Nucleolar RNA 71A Promotes Lung Cancer Cell Proliferation, Migration and Invasion via MAPK/ERK Pathway.", "doi": "10.7150/jca.31077", "pmid": "31258730", "authors": ["Guiliang Tang", "Zihang Zeng", "Wenjie Sun", "Shuying Li", "Chengcheng You", "Fang Tang", "Shan Peng", "Shijing Ma", "Yuan Luo", "Jieyu Xu", "Xiaoli Tian", "Nannan Zhang", "Yan Gong", "Conghua Xie"], "journal": "Journal of Cancer", "year": 2019, "abstract": "Objective: Increasing evidence suggested that dysregulated small nucleolar RNAs (snoRNAs) were involved in tumor development. The roles of snoRNA 71A (SNORA71A) in the progression of non-small cell lung cancer (NSCLC) remained unclear. Methods: Dataset GSE19188 from Gene Expression Omnibus (GEO) database was downloaded to detect the expression levels of SNORA71A in NSCLC tissues. The biological significance of SNORA71A was explored by loss-of-function analysis both in vitro and in vivo. Results: SNORA71A was overexpressed in NSCLC tissues compared with normal tissues, and upregulated SNORA71A was significantly associated with worse survival of NSCLC patients. Knockdown of SNORA71A suppressed proliferation of both A549 and PC9 cells, and induced G0/G1 phase arrest. Knockdown of SNORA71A also suppressed xenograft tumor growth in mice. In addition, knockdown of SNORA71A inhibited cell invasion and migration and suppressed epithelial-mesenchymal transition. Furthermore, downregulated SNORA71A decreased the phosphorylation of MEK and ERK1/2 in the MAPK/ERK signal pathway. 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