Evidence map›Paper›PMID 29054988›Full record

ArticleMolecular cancer therapeutics2018

AKT1

Cleidson P Alves, Ipsita Dey-Guha, Sheheryar Kabraji, Albert C Yeh, Nilesh P Talele, Xavier Solé, Joeeta Chowdhury, Mari Mino-Kenudson, Massimo Loda, Dennis Sgroi and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Novel Mutations inCurrent issues in molecular biology · 2024
    Article
  3. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Investigation into theFrontiers in pharmacology · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. AKT1NPJ breast cancer · 2019
    Article
  12. Review
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

14 authors at 4 institutions in 2 countries.

Cleidson P Alves *Massachusetts General Hospital Cancer Center, Boston, Massachusetts.
Ipsita Dey-Guha *Massachusetts General Hospital Cancer Center, Boston, Massachusetts.
Sheheryar KabrajiMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Albert C YehMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Nilesh P TaleleMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Xavier SoléMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Joeeta ChowdhuryMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Mari Mino-KenudsonMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Massimo LodaHarvard Medical School, Boston, Massachusetts.
Dennis SgroiMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Anne-Lise Borresen-DaleInstitute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Hege G RussnesInstitute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Kenneth N RossMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Sridhar RamaswamyMassachusetts General Hospital Cancer Center, Boston, Massachusetts. sridhar.ramaswamy@me.com.
Harvard University · USMassachusetts General Hospital · USUniversity of Oslo · NODana-Farber Cancer Institute · US

Funding

(PQC6) Molecular Determinants of Quiescent Cancer CellsR01CA185086 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI VASUDEVAN, SHOBHA · 2014 to 2017
$1.8M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA185086
6 · The paper itself

Abstract

Human tumor growth depends on rapidly dividing cancer cells driving population expansion. Even advanced tumors, however, contain slowly proliferating cancer cells for reasons that remain unclear. Here, we selectively disrupt the ability of rapidly proliferating cancer cells to spawn AKT1

Indexed as

AnimalsCell Line, TumorCell ProliferationCell Transformation, NeoplasticFemaleHCT116 CellsHeterograftsHumansMCF-7 CellsMiceNeoplasmsProto-Oncogene Proteins c-aktAKT1 protein, humanProto-Oncogene Proteins c-akt

Identifiers

PMID29054988
PMCPMC5752592
OpenAlexW2765934395

What OpenQuestion holds

Textmetadata
LicenceTDM
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.