Evidence map›Paper›PMID 38791105›Full record

ReviewInternational journal of molecular sciences2024

PROTACs in Ovarian Cancer: Current Advancements and Future Perspectives.

Makenzie Vorderbruggen, Carlos A Velázquez-Martínez, Amarnath Natarajan, Adam R Karpf

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

4 authors.

Makenzie VorderbruggenEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, NE 68198-6805, USA.
Carlos A Velázquez-MartínezFaculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, AB T6G 2E1, Canada.ORCID 0000-0003-4535-1835
Amarnath NatarajanEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, NE 68198-6805, USA.ORCID 0000-0001-5067-0203
Adam R KarpfEppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha, NE 68198-6805, USA.ORCID 0000-0002-0866-0666

Funding

CHEMICAL CARCINOGENESIS &CANCER BIOLOGYT32CA009476 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Jennifer D. Black · 1988 to 2026
$6.2M
Development of Quinoxaline Based IKKbeta Inhibitors for Kras Driven CancersR01CA197999 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Amarnath (Amar) Natarajan · 2016 to 2026
$3.3M
UPR Activators for Cancer TherapyR01CA260749 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Amarnath (Amar) Natarajan · 2022 to 2026
$1.7M
Targeting RHNO1 in Ovarian CancerR21CA273399 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KARPF, ADAM R. · 2023 to 2024
$384k
NCI NIH HHS R01 CA197999NCI NIH HHS R01 CA260749NCI NIH HHS R21 CA273399NCI NIH HHS T32 CA009476
6 · The paper itself

Abstract

Ovarian cancer is the deadliest gynecologic malignancy. The majority of patients diagnosed with advanced ovarian cancer will relapse, at which point additional therapies can be administered but, for the most part, these are not curative. As such, a need exists for the development of novel therapeutic options for ovarian cancer patients. Research in the field of targeted protein degradation (TPD) through the use of proteolysis-targeting chimeras (PROTACs) has significantly increased in recent years. The ability of PROTACs to target proteins of interest (POI) for degradation, overcoming limitations such as the incomplete inhibition of POI function and the development of resistance seen with other inhibitors, is of particular interest in cancer research, including ovarian cancer research. This review provides a synopsis of PROTACs tested in ovarian cancer models and highlights PROTACs characterized in other types of cancers with potential high utility in ovarian cancer. Finally, we discuss methods that will help to enable the selective delivery of PROTACs to ovarian cancer and improve the pharmacodynamic properties of these agents.

Indexed as

Antineoplastic AgentsOvarian NeoplasmsProteolysisAnimalsFemaleHumansMolecular Targeted TherapyProteolysis Targeting ChimeraAntineoplastic AgentsProteolysis Targeting Chimerahigh-grade serous ovarian cancerovarian cancerPROTACtargeted protein degradation

Identifiers

PMID38791105
PMCPMC11121112

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.