Evidence map›Paper›PMID 38817073›Full record

ArticleOral diseases2024

LncRNA EIF3J-DT promotes chemoresistance in oral squamous cell carcinoma.

Seon Hyun Kim, Hye Jung Kim, Yeong Joo Kim, Yun Hak Kim, Hae Ryoun Park

Abstract read
In one paragraph

Article in Oral diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. The ATG14: multi-layer autophagy control and an emerging therapeutic target in cancer.Apoptosis : an international journal on programmed cell death · 2026
    Review
  3. Review
  4. 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.

Seon Hyun KimPeriodontal Disease Signaling Network Research Center (MRC), School of Dentistry, Pusan National University, Yangsan, Korea.
Hye Jung KimPeriodontal Disease Signaling Network Research Center (MRC), School of Dentistry, Pusan National University, Yangsan, Korea.ORCID 0000-0002-3767-9665
Yeong Joo KimInterdisciplinary Program of Genomic Data Science, Pusan National University, Yangsan, Korea.
Yun Hak KimPeriodontal Disease Signaling Network Research Center (MRC), School of Dentistry, Pusan National University, Yangsan, Korea.ORCID 0000-0002-9796-8266
Hae Ryoun ParkPeriodontal Disease Signaling Network Research Center (MRC), School of Dentistry, Pusan National University, Yangsan, Korea.ORCID 0000-0003-1908-0824

Funding

Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT RS-2023-00209335National Research Foundation of Korea (NRF) Grant funded by the Korea government (MSIT) NRF-2018R1A5A2023879
6 · The paper itself

Abstract

objectivesThis study aimed to screen oral squamous cell carcinoma (OSCC) diagnostic and prognostic candidates and investigate the potential functions and mechanisms of candidates in the chemoresistance of OSCC cell lines. MATERIALS AND

methodsDifferential expression profiling of lncRNA was performed in a large cohort of OSCC patients from the Cancer Genome Atlas database to identify OSCC diagnostic and prognostic candidates. Taxol resistance in OSCC cell lines was analyzed using MTT assay. OSCC cell lines transfected with EIF3J-DT pcDNA or siRNA were used to determine its regulatory effects on apoptosis, cell cycle distribution and autophagy using flow cytometry and western blot.

resultsWe identified EIF3J-DT as a candidate for OSCC diagnosis and prognosis. The expression level of EIF3J-DT in OSCC cell lines correlates with taxol resistance. EIF3J-DT silencing attenuated taxol resistance, and EIF3J-DT overexpression enhanced taxol resistance in OSCC cell lines. Silencing of EIF3J-DT reduced taxol resistance by inducing apoptosis, cell cycle arrest, and ATG14-mediated autophagy inhibition in OSCC cell lines.

conclusionsWe found that EIF3J-DT induced chemoresistance by regulating apoptosis, cell cycle, and autophagy in OSCC cell lines, which EIF3J-DT might provide a novel therapeutic approach for OSCC as well as a diagnostic and prognostic factor.

Indexed as

ApoptosisAutophagyCarcinoma, Squamous CellDrug Resistance, NeoplasmMouth NeoplasmsPaclitaxelRNA, Long NoncodingAntineoplastic Agents, PhytogenicCell Line, TumorHumansMalePrognosisAntineoplastic Agents, PhytogenicPaclitaxelRNA, Long Noncodingapoptosiscell proliferationchemoresistanceEIF3J‐DTlong non‐coding RNAoral squamous cell carcinoma

Identifiers

PMID38817073
PMCPMC11610658

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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.