Evidence map›Paper›PMID 33342344›Full record

ArticleCell cycle (Georgetown, Tex.)2021

IncRNA ZFAS1 contributes to the radioresistance of nasopharyngeal carcinoma cells by sponging hsa-miR-7-5p to upregulate ENO2.

Jiaojiao Peng, Feng Liu, Hong Zheng, Qi Wu, Shixi Liu

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  9. BeyondMolecular therapy oncolytics · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. ENO3 promotes colorectal cancer progression by enhancing cell glycolysis.Medical oncology (Northwood, London, England) · 2022
    Article
  16. Article
  17. Article
  18. Review
  19. MiR-7 in Cancer Development.Biomedicines · 2021
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jiaojiao PengDepartment of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University , Sichuan, China.
Feng LiuDepartment of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University , Sichuan, China.
Hong ZhengDepartment of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University , Sichuan, China.
Qi WuDepartment of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University , Sichuan, China.
Shixi LiuDepartment of Otolaryngology, Head and Neck Surgery, West China Hospital, Sichuan University , Sichuan, China.
Sichuan University · CNWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous research revealed that lncRNA ZFAS1 could promote nasopharyngeal carcinoma (NPC) by inhibiting its downstream target axis. However, the association between ZFAS1 and radioresistant NPC cells is unclear. This study aimed to explore the roles of ZFAS1 in the radioresistance of NPC. Bioinformatics analysis was conducted to identify the significant factors (ENO2 and miR-7-5p) that contributed to the radioresistance of NPC cells. After performing qRT-PCR analysis, we found that the expression of ZFAS1 and ENO2 was upregulated in NPC cells but that the miR-7-5p expression was downregulated in the same samples. Apart from that, we noticed that ZFAS1 inhibition enhanced the sensitivity of NPC cells to radiation therapy by repressing cell proliferation and promoting cell apoptosis. Subsequently, we found that ZFAS1 could sponge miR-7-5p to upregulate ENO2, which was the target of miR-7-5p. Experimental results also indicated that the suppression of miR-7-5p inhibited the sensitivity of NPC cells to radiation therapy, thereby suppressing ENO2 expression. Overall, our findings suggested that ZFAS1 contributed to the radioresistance of NPC cells by regulating the miR-7-5p/ENO2 axis and that ZFAS1 might be a potential therapeutic target for addressing the radioresistance of NPC cells.

Indexed as

Cell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMicroRNAsNasopharyngeal CarcinomaNasopharyngeal NeoplasmsPhosphopyruvate HydrataseRNA, Long NoncodingTranscriptional ActivationUp-RegulationENO2 protein, humanMicroRNAsMIRN7-1 microRNA, humanPhosphopyruvate HydrataseRNA, Long NoncodingZFAS1 long non-coding RNA, humanglycolysis (Warburg effect)HIF1-alphaLncRNAnasopharyngeal carcinoma and tumor resistancetumor suppressor

Identifiers

PMID33342344
PMCPMC7849681
OpenAlexW3114435021

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.