Evidence map›Paper›PMID 26234676›Full record

ArticleOncogene2016

TRM6/61 connects PKCα with translational control through tRNAi(Met) stabilization: impact on tumorigenesis.

F Macari, Y El-Houfi, G Boldina, H Xu, S Khoury-Hanna, J Ollier, L Yazdani, G Zheng, I Bièche, N Legrand and 14 more

Registry-linked trialOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06575452 (Using the Epitranscriptome to Diagnose and Treat Gliomas), which is not on this map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
0.8field-weighted citation impact, top 29% 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.

NCT06575452 narecruitingnot on this mapstarted 2026, after this paper: background citation

Using the Epitranscriptome to Diagnose and Treat Gliomas

TypeinterventionalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2026 to 2031Enrolled228ConditionsGliomaArmsBlood, urine and tumoral tissue samples, Tumoral tissue samples
3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. ALKBH3-regulated mActa pharmaceutica Sinica. B · 2025
    Article
  10. TRMT10A regulates tRNA-ArgCCT mCell death & disease · 2025
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. The NClinical and translational medicine · 2025
    Article
  18. Review
  19. Review
  20. Article

6 more citing papers are in PubMed but not listed here.

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

24 authors at 9 institutions in 4 countries.

F MacariDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Y El-HoufiDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
G BoldinaInstitut Curie, Centre de Recherche, Orsay, France.
H XuDepartment of Molecular Biology, Umeå University Umeå Sweden.
S Khoury-HannaDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
J OllierDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
L YazdaniDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
G ZhengDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
I BiècheLaboratory of Oncogenetic, Institut Curie, Hopital René Huguenin, St-Cloud, France.
N LegrandDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
D PauletLaboratoire d'Informatique, de Robotique et de Microélectronique de Montpellier, Montpellier, France.
S DurrieuUniversity of Bordeaux, Institut Européen de Chimie et Biologie, ARNA Laboratory, Pessac, France.
A ByströmDepartment of Molecular Biology, Umeå University Umeå Sweden.
S DelbecqLaboratoire de Biologie Cellulaire et Moléculaire, Université Montpellier 1, Montpellier, France.
B LapeyreUSR 3278, CNRS-UPHE-UPVD, CRIOBE, Moorea, French Polynesia.
L BauchetDepartment of Neurosurgery, Hôpital Gui de Chauliac, Montpellier, France.
J PannequinDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
F HollandeDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
T PanDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
M TeichmannUniversity of Bordeaux, Institut Européen de Chimie et Biologie, ARNA Laboratory, Pessac, France.
S VagnerInstitut Curie, Centre de Recherche, Orsay, France.
A DavidDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
A ChoquetDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
D JoubertDepartment of Oncology, CNRS, UMR-5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Centre National de la Recherche Scientifique · FRUmeå University · SEUniversité de Bordeaux · FRUniversité Paris-Sud · FRUniversity of Chicago · USHôpital Gui de Chauliac · FRHôpital René Huguenin · FRLaboratoire d'Informatique, de Robotique et de Microélectronique de Montpellier · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence suggests that changes of the protein synthesis machinery alter translation of specific mRNAs and participate in malignant transformation. Here we show that protein kinase C α (PKCα) interacts with TRM61, the catalytic subunit of the TRM6/61 tRNA methyltransferase. The TRM6/61 complex is known to methylate the adenosine 58 of the initiator methionine tRNA (tRNAi(Met)), a nuclear post-transcriptional modification associated with the stabilization of this crucial component of the translation-initiation process. Depletion of TRM6/61 reduced proliferation and increased death of C6 glioma cells, effects that can be partially rescued by overexpression of tRNAi(Met). In contrast, elevated TRM6/61 expression regulated the translation of a subset of mRNAs encoding proteins involved in the tumorigenic process and increased the ability of C6 cells to form colonies in soft agar or spheres when grown in suspension. In TRM6/61/tRNAi(Met)-overexpressing cells, PKCα overexpression decreased tRNAi(Met) expression and both colony- and sphere-forming potentials. A concomitant increase in TRM6/TRM61 mRNA and tRNAi(Met) expression with decreased expression of PKCα mRNA was detected in highly aggressive glioblastoma multiforme as compared with Grade II/III glioblastomas, highlighting the clinical relevance of our findings. Altogether, we suggest that PKCα tightly controls TRM6/61 activity to prevent translation deregulation that would favor neoplastic development.

Indexed as

ApoptosisBiomarkers, TumorCarcinogenesisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGlioblastomaHumansMethionineProtein Kinase C-alphaRNA, TransfertRNA MethyltransferasesBiomarkers, TumorMethioninePRKCA protein, humanProtein Kinase C-alphaRNA, TransferTRMT61A protein, humantRNA Methyltransferases

Identifiers

PMID26234676
OpenAlexW1955371253

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.