Evidence map›Paper›PMID 39210542›Full record

ReviewClinical and translational medicine2024

Ecological and evolutionary dynamics to design and improve ovarian cancer treatment.

Grace Y Q Han, Monica Alexander, Julia Gattozzi, Marilyn Day, Elayna Kirsch, Narges Tafreshi, Raafat Chalar, Soraya Rahni, Gabrielle Gossner, William Burke and 1 more

Abstract readReview
In one paragraph

Review in Clinical and translational medicine, 2024. 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. Review
  2. Article
  3. Review
  4. Review
  5. Targeting tumor transition windows.Exploration of targeted anti-tumor therapy · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  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

11 authors.

Grace Y Q HanRenaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.ORCID 0009-0004-3172-2521
Monica AlexanderDepartment of Molecular and Cellular Biology, Stony Brook University, Stony Brook, New York, USA.ORCID 0009-0000-3351-1913
Julia GattozziDepartment of Molecular and Cellular Pharmacology, Stony Brook University, Stony Brook, New York, USA.
Marilyn DayDepartment of Obstetrics and Gynecology, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.
Elayna KirschDepartment of Obstetrics and Gynecology, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.
Narges TafreshiCellinfinity Bio, New Haven, Connecticut, USA.
Raafat ChalarStony Brook Cancer Center, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.
Soraya RahniStony Brook University, Stony Brook, New York, USA.
Gabrielle GossnerDepartment of Obstetrics and Gynecology, Stony Brook University Hospital, Stony Brook, New York, USA.
William BurkeDepartment of Obstetrics and Gynecology, Stony Brook University Hospital, Stony Brook, New York, USA.
Mehdi DamaghiStony Brook Cancer Center, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.

Funding

Radiomics and Pathomics to predict upstaging of DCISR01CA249016 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DAMAGHI, MEHDI, NIELL, BETHANY LYNN · 2021 to 2025
$3.4M
Ecology and Evolution of Breast CarcinogenesisU01CA261841 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DAMAGHI, MEHDI, SIQUEIRA SILVA, ARIOSTO S · 2021 to 2025
$3.0M
Training Program in Pharmacological SciencesT32GM144304 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HOLLY A COLOGNATO · 2022 to 2026
$1.8M
NCI NIH HHS R01 CA249016NCI NIH HHS U01 CA261841NCI NIH HHS U01CA261841-01NIGMS NIH HHS T32 GM144304NIH HHS R01CA249016-01Physical Sciences Oncology Network at the National Cancer Institute through R01CA249016-01Physical Sciences Oncology Network at the National Cancer Institute through U01CA261841-01
6 · The paper itself

Abstract

Ovarian cancer ecosystems are exceedingly complex, consisting of a high heterogeneity of cancer cells. Development of drugs such as poly ADP-ribose polymerase (PARP) inhibitors, targeted therapies and immunotherapies offer more options for sequential or combined treatments. Nevertheless, mortality in metastatic ovarian cancer patients remains high because cancer cells consistently develop resistance to single and combination therapies, urging a need for treatment designs that target the evolvability of cancer cells. The evolutionary dynamics that lead to resistance emerge from the complex tumour microenvironment, the heterogeneous populations, and the individual cancer cell's plasticity. We propose that successful management of ovarian cancer requires consideration of the ecological and evolutionary dynamics of the disease. Here, we review current options and challenges in ovarian cancer treatment and discuss principles of tumour evolution. We conclude by proposing evolutionarily designed strategies for ovarian cancer, with the goal of integrating such principles with longitudinal, quantitative data to improve the treatment design and management of drug resistance. KEY POINTS/HIGHLIGHTS: Tumours are ecosystems in which cancer and non-cancer cells interact and evolve in complex and dynamic ways. Conventional therapies for ovarian cancer inevitably lead to the development of resistance because they fail to consider tumours' heterogeneity and cellular plasticity. Eco-evolutionarily designed therapies should consider cancer cell plasticity and patient-specific characteristics to improve clinical outcome and prevent relapse.

Indexed as

Ovarian NeoplasmsFemaleHumansTumor Microenvironmentovarian cancerphenotypic plasticitytumour ecologytumour evolutiontumour microenvironment

Identifiers

PMID39210542
PMCPMC11362027

What OpenQuestion holds

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Registered trials

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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.