Evidence map›Paper›PMID 34463208›Full record

ArticleBioengineered2021

Long non-coding RNA LINC01207 promotes cell proliferation and migration but suppresses apoptosis and autophagy in oral squamous cell carcinoma by the microRNA-1301-3p/lactate dehydrogenase isoform A axis.

Xiaolin Lu, Liling Chen, Yang Li, Rong Huang, Xiangfeng Meng, Fangfang Sun

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Serums miR-24-3p and miR-1301-3p as Potential Biomarkers in MEN1 Syndrome.International journal of molecular sciences · 2025
    Article
  5. Review
  6. Autophagy in oral cancer: Promises and challenges (Review).International journal of molecular medicine · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. The role of LncRNA-mediated autophagy in cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Article
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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

6 authors at 2 institutions in 1 country.

Xiaolin LuDepartment of Maxillofacial Surgery, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.
Liling ChenDepartment of Prosthodontics, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.
Yang LiDepartment of Prosthodontics, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.
Rong HuangDepartment of Prosthodontics, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.
Xiangfeng MengDepartment of Prosthodontics, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.
Fangfang SunDepartment of Prosthodontics, Nanjing Stomatological Hospital Medical School of Nanjing University, Nanjing, China.ORCID 0000-0002-7322-2566
Nanjing Medical University · CNShanghai Traditional Chinese Medicine Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) have been reported to participate in the progression of various cancers, including oral squamous cell carcinoma (OSCC). This study aims to find out whether lncRNA LINC01207 regulates the progression of OSCC. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) was conducted to evaluate gene expression in OSCC cells and tissues. Cell viability, proliferation, migration, apoptosis, and autophagy were detected using Cell Counting Kit-8 (CCK-8), colony formation, Transwell assays, flow cytometry, and western blot analysis. Luciferase reporter and RNA immunoprecipitation (RIP) assays were conducted to assess the interactions among genes. We found that LINC01207 was overexpressed in OSCC cells and tissues. LINC01207 silencing inhibited OSCC cell proliferation and migration but promoted apoptosis and autophagy, and LINC01207 overexpression had an opposite result. LINC01207 interacted with microRNA-1301-3p (miR-1301-3p) while lactate dehydrogenase isoform A (LHDA) was targeted by miR1301-3p. Effects caused by LINC01207 downregulation on OSCC cells were reversed by overexpression of LDHA. Overall, LINC01207 promotes OSCC progression via the miR-1301-3p/LDHA axis.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsApoptosisAutophagyCell Line, TumorCell MovementCell ProliferationHumansL-Lactate DehydrogenaseMicroRNAsMouthRNA, Long NoncodingLDHA protein, humanL-Lactate DehydrogenaseMicroRNAsMIRN1301 microRNA, humanRNA, Long Noncodingautophagyldhalinc01207miR-1301-3pOSCC

Identifiers

PMID34463208
PMCPMC8806684
OpenAlexW3196684256

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.