Evidence map›Paper›PMID 33691584›Full record

ReviewCell cycle (Georgetown, Tex.)2021

Regulation of DNA duplication by the mTOR signaling pathway.

Zhengfu He, Peter J Houghton, Terence M Williams, Changxian Shen

Abstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2021. 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
–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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Frontiers in microbiology · 2025
    Article
  5. Review
  6. Cell cycle re-entry in the agingbioRxiv : the preprint server for biology · 2024
    Article
  7. Polyploidy and mTOR signaling: a possible molecular link.Cell communication and signaling : CCS · 2024
    Review
  8. Review
  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

4 authors.

Zhengfu HeDepartment of Thoracic Surgery, Sir Run Run Shaw Hospital, College of Medicine Zhejiang University, Hangzhou, China.
Peter J HoughtonThe Greehey Children's Cancer Research Institute, the University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Terence M WilliamsDepartment of Radiation Oncology, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.ORCID 0000-0002-1020-0845
Changxian ShenDepartment of Radiation Oncology, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, USA.

Funding

Developing BRAF mutant and BRAF wild-type selective strategies for radiosensitization in Anaplastic Thyroid CancerR01CA246553 · NCI · OHIO STATE UNIVERSITY · PI WILLIAMS, TERENCE MARQUES · 2020 to 2025
$2.0M
NCI NIH HHS R01 CA246553
6 · The paper itself

Abstract

Accurate and complete DNA replication and separation are essential for genetic information inheritance and organism maintenance. Errors in DNA duplication are the main source of genetic instability. Understanding DNA duplication regulation is the key to elucidate the mechanisms and find treatment strategies for human genetic disorders, especially cancer. The mechanistic target of rapamycin (mTOR) is a central regulator of cell growth and proliferation by integrating and processing extracellular and intracellular signals to monitor the well-being of cell physiology. mTOR signaling dysregulation is associated with many human diseases including cancer and diabetes. Emerging evidence has demonstrated that mTOR signaling plays a key role in DNA duplication. We herein review the current knowledge of mTOR signaling in the regulation of DNA replication origin licensing, replication fork progression, and stabilization.

Indexed as

AnimalsCell ProliferationDNA ReplicationHumansSignal TransductionTOR Serine-Threonine KinasesMTOR protein, humanTOR Serine-Threonine Kinasescell cycleDNA repairmTOR; DNA replication origin licensingreplication fork progressionreplication fork stabilization

Identifiers

PMID33691584
PMCPMC8098070

What OpenQuestion holds

Textmetadata
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.