Evidence map›Paper›PMID 33669867›Full record

ArticleInternational journal of molecular sciences2021

Phosphoinositide 3-Kinase (PI3K) Reactive Oxygen Species (ROS)-Activated Prodrug in Combination with Anthracycline Impairs PI3K Signaling, Increases DNA Damage Response and Reduces Breast Cancer Cell Growth.

Rosalin Mishra, Long Yuan, Hima Patel, Aniruddha S Karve, Haizhou Zhu, Aaron White, Samar Alanazi, Pankaj Desai, Edward J Merino, Joan T Garrett

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. New 1,3-diphenyl-1Heliyon · 2024
    Article
  7. Regulation of PI3K signaling in cancer metabolism and PI3K-targeting therapy.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. PI3K Inhibitors in Cancer: Clinical Implications and Adverse Effects.International journal of molecular sciences · 2021
    Review
  13. 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

10 authors at 2 institutions in 1 country.

Rosalin MishraDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.ORCID 0000-0002-9808-8797
Long YuanDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Hima PatelDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Aniruddha S KarveDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.ORCID 0000-0002-1617-4828
Haizhou ZhuDepartment of Chemistry, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Aaron WhiteDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.ORCID 0000-0003-4844-4973
Samar AlanaziDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Pankaj DesaiDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Edward J MerinoDepartment of Chemistry, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
Joan T GarrettDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.
University of Cincinnati Medical Center · USUniversity of Cincinnati · US

Funding

Limiting UV-induced genome instability with self-cycling antioxidant reagentsR15ES029675 · NIEHS · UNIVERSITY OF CINCINNATI · PI MERINO, EDWARD J · 2019 to 2019
$461k
NIEHS NIH HHS R15 ES029675Office of Research, University of Cincinnati R40309
6 · The paper itself

Abstract

RIDR-PI-103 is a novel reactive oxygen species (ROS)-induced drug release prodrug with a self-cyclizing moiety linked to a pan-PI3K inhibitor (PI-103). Under high ROS, PI-103 is released in a controlled manner to inhibit PI3K. The efficacy and bioavailability of RIDR-PI-103 in breast cancer remains unexplored. Cell viability of RIDR-PI-103 was assessed on breast cancer cells (MDA-MB-231, MDA-MB-361 and MDA-MB-453), non-tumorigenic MCF10A and fibroblasts. Matrigel colony formation, cell proliferation and migration assays examined the migratory properties of breast cancers upon treatment with RIDR-PI-103 and doxorubicin. Western blots determined the effect of doxorubicin ± RIDR-PI-103 on AKT activation and DNA damage response. Pharmacokinetic (PK) studies using C57BL/6J mice determined systemic exposure (plasma concentrations and overall area under the curve) and T

Indexed as

DNA DamageSignal TransductionAnimalsAnthracyclinesBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationCell SurvivalCollagenDoxorubicinDrug CombinationsFemaleFibroblastsFuransHumansAnthracyclinesCollagenDoxorubicinDrug CombinationsFuransLamininmatrigelPhosphatidylinositol 3-KinasesPI103ProdrugsProteoglycansPyridinesPyrimidinesReactive Oxygen Speciesbreast cancerdoxorubicinreactive oxygen speciesRIDR-PI-103

Identifiers

PMID33669867
PMCPMC7923228
OpenAlexW3132918768

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.