Evidence map›Paper›PMID 27789731›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2017

Evaluation of Akt and RICTOR Expression Levels in Astrocytomas of All Grades.

Arthur William Alvarenga, Luis Eduardo Machado, Bruna Roz Rodrigues, Fernanda Cristina Sulla Lupinacci, Paulo Sanemastu, Eduardo Matta, Martín Roffé, Luís Fernando Bleggi Torres, Isabela Werneck da Cunha, Vilma Regina Martins and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. mTOR hyperactivity andPathology oncology research : POR · 2024
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Overexpression of mTOR and p(240-244)S6 in IDH1 Wild-Type Human Glioblastomas Is Predictive of Low Survival.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2018
    Article
  13. Review
  14. Article
  15. Article
  16. 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.

Arthur William AlvarengaInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Luis Eduardo MachadoInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Bruna Roz RodriguesInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Fernanda Cristina Sulla LupinacciInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Paulo SanemastuNeurosurgery Department (PS).
Eduardo MattaInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Martín RofféInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Luís Fernando Bleggi TorresA.C.Camargo Cancer Center, São Paulo, Brazil, and Institute Pelé-Pequeno Príncipe for Research on Pediatric Cancer, Curitiba, Brazil (LFBT).
Isabela Werneck da CunhaPathology Department (IWC).
Vilma Regina MartinsInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
Glaucia Noeli Maroso HajjInternational Research Center (AWA, LEM, BRR, FCSL, EM, MR, VRM, GNMH).
AC Camargo Hospital · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mammalian target of rapamycin (mTOR) binds to several protein partners and forms two complexes, termed mTOR complexes 1 and 2 (mTORC1/2), that differ in components, substrates, and regulation. mTORC2 contains the protein Rapamycin-insensitive companion of mTOR (RICTOR); phosphorylates kinases of the AGC family, such as Akt; and controls the cytoskeleton. Even though the regulation of mTORC2 activity remains poorly understood, the hyperactivation of this signaling pathway has been shown to contribute to the oncogenic properties of gliomas in experimental models. In this work, we evaluated expression and phosphorylation of Akt, and expression of RICTOR and Ki-67 in 195 human astrocytomas of different grades (38 cases of grade I, 49 grade II, 15 grade III, and 93 grade IV) and 30 normal brains. Expression and phosphorylation of Akt increased with histological grade and correlated with a worse overall survival in glioblastomas (GBMs). RICTOR was overexpressed in grade I and II astrocytomas and demonstrated a shift to nuclear localization in GBMs. Nuclear RICTOR was associated to increased proliferation in GBMs. Our results point to an increase in total and phosphorylated Akt in high-grade gliomas and to a possible role of RICTOR in proliferations of high-grade GBM cells.

Indexed as

AdolescentAdultAgedAstrocytomaBrainBrain NeoplasmsCarrier ProteinsCell ProliferationChildChild, PreschoolFemaleGlioblastomaHumansKi-67 AntigenMaleMiddle AgedCarrier ProteinsKi-67 AntigenProto-Oncogene Proteins c-aktRapamycin-Insensitive Companion of mTOR ProteinRICTOR protein, humanAktastrocytomamTORRICTOR

Identifiers

PMID27789731
PMCPMC5256195
OpenAlexW2542759190

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.