Evidence map›Paper›PMID 38970092›Full record

ReviewCancer cell international2024

The role of lncRNA NEAT1 in human cancer chemoresistance.

Feng Long, Xue Li, Jingyu Pan, Hailin Ye, Cuixia Di, Yong Huang, Jiawei Li, Xuan Zhou, Huiyi Yi, Qiaozhen Huang and 1 more

Abstract readReview
In one paragraph

Review in Cancer cell international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Exosomal NEAT1 from tumor stem cells induces SIRPAJournal of experimental & clinical cancer research : CR · 2026
    Article
  5. Article
  6. Review
  7. TheJournal of gastrointestinal oncology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. 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

11 authors.

Feng Long *School of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Xue Li *School of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Jingyu PanSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Hailin YeSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Cuixia DiDepartment of Medical Physics, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, China.
Yong HuangSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Jiawei LiSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Xuan ZhouSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Huiyi YiSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Qiaozhen HuangSchool of Basic Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Jing SiDepartment of Medical Physics, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, China. sijing@impcas.ac.cn.

Funding

"Double First-Class" Key Research Projects in Gansu Province GSSYLXM-01Flagship Education Projects 2021jyjbgs-03Innovation Fund Program for Higher Education Teachers 2024A-088Open Project of Dunhuang Key Laboratory of Medicine and Translational Education DHYX22-10the National Key R and D Program of China 2018YFE0205100
6 · The paper itself

Abstract

Chemotherapy is currently one of the most effective methods in clinical cancer treatment. However, chemotherapy resistance is an important reason for poor chemotherapy efficacy and prognosis, which has become an urgent problem to be solved in the field of cancer chemotherapy. Therefore, it is very important to deeply study and analyze the mechanism of cancer chemotherapy resistance and its regulatory factors. Long non-coding RNA nuclear paraspeckle assembly transcript 1 (LncRNA NEAT1) has been shown to be closely associated with chemotherapy resistance in cancer. NEAT1 induces cancer cell resistance to chemotherapeutic drugs by regulating cell apoptosis, cell cycle, drug transport and metabolism, DNA damage repair, EMT, autophagy, cancer stem cell characteristics, and metabolic reprogramming. This indicates that NEAT1 may be an important target to overcome chemotherapy resistance and is expected to be a potential biomarker to predict the effect of chemotherapy. This article summarizes the expression characteristics and clinical characteristics of NEAT1 in different cancers, and deeply discusses the regulatory role of NEAT1 in cancer chemotherapy resistance and related molecular mechanisms, aiming to clarify NEAT1 as a new target to overcome cancer chemotherapy resistance and the feasibility of chemotherapy sensitizers, with a view to providing a potential therapeutic direction for overcoming the dilemma of cancer resistance in the future.

Indexed as

CancerChemotherapy resistanceMechanism of actionNEAT1

Identifiers

PMID38970092
PMCPMC11227196

What OpenQuestion holds

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Registered trials

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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.