Evidence map›Paper›PMID 29093603›Full record

ArticleGeburtshilfe und Frauenheilkunde2017

PI3K/AKT/mTOR Pathway in Ovarian Cancer Treatment: Are We on the Right Track?

Maria Luisa Gasparri, Erlisa Bardhi, Ilary Ruscito, Andrea Papadia, Ammad Ahmad Farooqi, Claudia Marchetti, Giorgio Bogani, Irene Ceccacci, Michael D Mueller, Pierluigi Benedetti Panici

Open access · hybridAbstract read
In one paragraph

Article in Geburtshilfe und Frauenheilkunde, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Autophagy in Ovarian Cancer, an Opportunity or an Additional Threat?International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Navigating the Complexities of Cancer Treatment-Induced Hypertension.Journal of cardiovascular development and disease · 2025
    Review
  7. Review
  8. Review
  9. Loss of phosphatase and tensin homolog (Cancer pathogenesis and therapy · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

12 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

10 authors at 4 institutions in 3 countries.

Maria Luisa GasparriDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Erlisa BardhiDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Ilary RuscitoDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Andrea PapadiaDepartment of Obstetrics and Gynecology, University of Berne, Berne, Switzerland.
Ammad Ahmad FarooqiLaboratory for Translational Oncology and Personalized Medicine, Rashid Latif Medical College, Lahore, Pakistan.
Claudia MarchettiDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Giorgio BoganiDepartment of Gynecologic Oncology, IRCCS National Cancer Institute, Milan, Italy.
Irene CeccacciDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Michael D MuellerDepartment of Obstetrics and Gynecology, University of Berne, Berne, Switzerland.
Pierluigi Benedetti PaniciDepartment of Gynecology, Obstetrics and Urology, "Sapienza" University of Rome, Rome, Italy.
Sapienza University of Rome · ITUniversity of Bern · CHIstituti di Ricovero e Cura a Carattere Scientifico · ITRashid Latif Medical College · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The high recurrence rate and the low overall survival in ovarian cancer suggest that a more specific therapeutic approach in addition to conventional treatment is required. Translational and clinical research is investigating new molecular targets in order to find an alternative way to affect tumor growth and to minimize the overlap of toxicity of antiblastic agents. Given its implication in many cellular activities including regulation of cell growth, motility, survival, proliferation, protein synthesis, autophagy, transcription, as well as angiogenesis, PI3K/AKT/mTOR is one of the most investigated intracellular signaling pathways. A dis-regulation of this pathway has been shown in several tumors, including ovarian cancer. In this setting, mTor proteins represent a potential target for inhibitors, which could ultimately play a pivotal role in counteracting cellular proliferation. Recently, mTor inhibitors have been approved in the treatment of pancreatic neuroendocrine tumors, mantle cell lymphoma and renal cancer. Clinical trials have assessed the safety of these drugs in ovarian cancer patients. Ongoing phase I and II studies are evaluating the oncologic outcome of mTor inhibitor treatment and its effect in combination with conventional chemotherapy and target agents.

Indexed as

everolimusmTOR inhibitorsovarian cancerPI3K/AKT/mTORtarget therapytemsirolimus

Identifiers

PMID29093603
PMCPMC5658232
OpenAlexW2766360518

What OpenQuestion holds

Textmetadata
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.