Evidence map›Paper›PMID 29057791›Full record

ReviewInternational journal of molecular sciences2017

Emerging Therapeutics to Overcome Chemoresistance in Epithelial Ovarian Cancer: A Mini-Review.

Robert Cornelison, Danielle C Llaneza, Charles N Landen

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 2 pooled it
12.7field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 2 syntheses or guidelines pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  6. Article
  7. Article
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  14. Advances in ovarian tumor stem cells and therapy.Cell biochemistry and biophysics · 2024
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Molecules (Basel, Switzerland) · 2023
    Review
  20. Targeting ovarian cancer stem cells: a new way out.Stem cell research & therapy · 2023
    Review

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

3 authors at 1 institution in 1 country.

Robert CornelisonDepartment of Obstetrics and Gynecology, University of Virginia, Charlottesville, VA 22908, USA. jrc3hg@virginia.edu.
Danielle C LlanezaDepartment of Obstetrics and Gynecology, University of Virginia, Charlottesville, VA 22908, USA. dcl5z@virginia.edu.
Charles N LandenDepartment of Obstetrics and Gynecology, University of Virginia, Charlottesville, VA 22908, USA. clanden@virginia.edu.
University of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Jay William FOX · 1987 to 2026
$72.1M
REPRODUCTIVE SCIENTIST TRAINING PROGRAMK12HD000849 · NICHD · WASHINGTON UNIVERSITY · PI Danny J Schust · 1988 to 2026
$33.2M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
NCI NIH HHS P30 CA044579NCI NIH HHS T32 CA009109NICHD NIH HHS K12 HD000849
6 · The paper itself

Abstract

Ovarian cancer is the fifth leading cause of cancer death among women and the most lethal gynecologic malignancy. One of the leading causes of death in high-grade serous ovarian cancer (HGSOC) is chemoresistant disease, which may present as intrinsic or acquired resistance to therapies. Here we discuss some of the known molecular mechanisms of chemoresistance that have been exhaustively investigated in chemoresistant ovarian cancer, including drug efflux pump multidrug resistance protein 1 (MDR1), the epithelial-mesenchymal transition, DNA damage and repair capacity. We also discuss novel therapeutics that may address some of the challenges in bringing approaches that target chemoresistant processes from bench to bedside. Some of these new therapies include novel drug delivery systems, targets that may halt adaptive changes in the tumor, exploitation of tumor mutations that leave cancer cells vulnerable to irreversible damage, and novel drugs that target ribosomal biogenesis, a process that may be uniquely different in cancer versus non-cancerous cells. Each of these approaches, or a combination of them, may provide a greater number of positive outcomes for a broader population of HGSOC patients.

Indexed as

Drug Resistance, NeoplasmAngiogenesis InhibitorsAnimalsATP-Binding Cassette TransportersCarcinoma, Ovarian EpithelialFemaleHumansNeoplasms, Glandular and EpithelialOvarian NeoplasmsPoly(ADP-ribose) Polymerase InhibitorsAngiogenesis InhibitorsATP-Binding Cassette TransportersPoly(ADP-ribose) Polymerase InhibitorschemoresistanceDNA damage and repairepithelial–mesenchymal transitionhigh-grade serous ovarian cancermultidrug resistance protein 1 (MDR1)ribosome biogenesis

Identifiers

PMID29057791
PMCPMC5666852
OpenAlexW2766094141

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.