Evidence map›Paper›PMID 29115614›Full record

ArticleMolecular medicine reports2018

Downregulation of TRIM28 inhibits growth and increases apoptosis of nude mice with non‑small cell lung cancer xenografts.

Lei Liu, Lei Zhang, Jianping Wang, Xuerong Zhao, Qian Xu, Yanjie Lu, Yanzhen Zuo, Long Chen, Jia Du, Yali Lian and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Multifaceted role ofMedComm · 2024
    Review
  3. TRIM28 in cancer and cancer therapy.Frontiers in genetics · 2024
    Review
  4. Review
  5. A TIAM1-TRIM28 complex mediates epigenetic silencing of protocadherins to promote migration of lung cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

11 authors at 1 institution in 1 country.

Lei LiuDepartment of Immunology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Lei ZhangDepartment of Community Care, Nursing Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Jianping WangDepartment of Immunology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Xuerong ZhaoDepartment of Immunology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Qian XuDepartment of Central Laboratory, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Yanjie LuDepartment of Pathology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Yanzhen ZuoDepartment of Pathology, Basic Medical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Long ChenDepartment of Central Laboratory, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Jia DuGrade 2013, Clinical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Yali LianGrade 2013, Clinical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Qin ZhangGrade 2013, Clinical Institute, Chengde Medical College, Chengde, Hebei 067000, P.R. China.
Affiliated Hospital of Chengde Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TRIM28 is a well‑known transcriptional co‑repressor of Kruppel‑associated box zinc finger proteins. The authors previously demonstrated that TRIM28 small interfering (si)RNA decreases cell proliferation and inhibits cell cycle progression in non‑small cell lung cancer (NSCLC) cell lines. The present study further demonstrated that the stable silencing of TRIM28 expression by a specific siRNA lentivirus vector significantly inhibited the growth and exerted obvious anti‑tumor effects in nude mice. The results of the terminal deoxynucleotidyl transferase‑mediated deoxyuridine triphosphate nick‑end labeling assay indicated that TRIM28 knockdown increased apoptosis. Furthermore, TRIM28 knockdown decreased the expression of B cell lymphoma (Bcl)‑2 and increased the expression of Bcl‑2 associated X, apoptosis regulator and p53 at the gene and protein levels. Auto‑antibodies to TRIM28 were present in 12.32% of the sera of the patients with NSCLC. The results suggest that TRIM28 knockdown may be effective against NSCLC, and TRIM28 antibodies have the potential to act as novel diagnostic and therapeutic tools.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAnimalsApoptosisApoptosis Regulatory ProteinsAutoantibodiesCarcinoma, Non-Small-Cell LungCase-Control StudiesCell CycleCell Line, TumorCell ProliferationFemaleGene Knockdown TechniquesHumansLung NeoplasmsApoptosis Regulatory ProteinsAutoantibodiesRNA, Small InterferingTripartite Motif-Containing Protein 28

Identifiers

PMID29115614
PMCPMC5780162
OpenAlexW2766880917

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.