Evidence map›Paper›PMID 37626587›Full record

ArticleBiomedicines2023

Combination Therapy with Trastuzumab and Niraparib: Quantifying Early Proliferative Alterations in HER2+ Breast Cancer Models.

Ameer Mansur, Patrick N Song, Yun Lu, Andrew C Burns, Luke Sligh, Eddy S Yang, Anna G Sorace

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

7 authors at 2 institutions in 1 country.

Ameer MansurDepartment of Biomedical Engineering, The University of Alabama, Birmingham, AL 35233, USA.ORCID 0009-0005-3750-7141
Patrick N SongDepartment of Radiology, The University of Alabama, Birmingham, AL 35233, USA.
Yun LuDepartment of Radiology, The University of Alabama, Birmingham, AL 35233, USA.ORCID 0000-0002-4785-3401
Andrew C BurnsDepartment of Biomedical Engineering, The University of Alabama, Birmingham, AL 35233, USA.ORCID 0000-0002-5028-6188
Luke SlighDepartment of Radiology, The University of Alabama, Birmingham, AL 35233, USA.
Eddy S YangDepartment of Radiation Oncology, University of Kentucky, Lexington, KY 40506, USA.ORCID 0000-0002-6450-2638
Anna G SoraceDepartment of Biomedical Engineering, The University of Alabama, Birmingham, AL 35233, USA.ORCID 0000-0002-3640-3966
University of Alabama at Birmingham · USUniversity of Kentucky · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
NRSA Training CoreTL1TR003106 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SAAG, KENNETH G · 2019 to 2023
$3.7M
UAB STEP-UP: Promoting Diversity through Team Mentored Research ExperiencesR25DK113652 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FOUAD, MONA N., GARVEY, W TIMOTHY · 2017 to 2024
$2.5M
UAB Predoctoral Training Grant in Translational and Molecular SciencesT32GM135028 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Mythreye Karthikeyan, RAKESH P. PATEL · 2021 to 2026
$1.6M
Personalizing immunotherapy in HER2+ breast cancer through quantitative imagingR01CA240589 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SORACE, ANNA C · 2020 to 2023
$1.6M
Mathematical modeling and molecular imaging to maximize response while minimizing toxicities from systemic therapies in preclinical models of breast cancerR01CA276540 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SORACE, ANNA C, YANKEELOV, THOMAS E · 2023 to 2025
$1.4M
NCATS NIH HHS TL1 TR003106NCI NIH HHS P30 CA013148NCI NIH HHS P30CA013148NCI NIH HHS R01 CA240589NCI NIH HHS R01CA240589NCI NIH HHS R01 CA276540NCI NIH HHS R01CA276540NIDDK NIH HHS 1R25DK113652NIGMS NIH HHS T32 GM135028
6 · The paper itself

Abstract

HER2-targeted treatments have improved survival rates in HER2+ breast cancer patients, yet poor responsiveness remains a major clinical obstacle. Recently, HER2+ breast cancer cells, both resistant and responsive to HER2-targeted therapies, have demonstrated sensitivity to poly-(ADP-ribose) polymerase (PARP) inhibition, independent of DNA repair deficiencies. This study seeks to describe biological factors that precede cell viability changes in response to the combination of trastuzumab and PARP inhibition. Treatment response was evaluated in HER2+ and HER2- breast cancer cells. Further, we evaluated the utility of 3'-Deoxy-3'-[

Indexed as

biomarkerscellular proliferationFLT–PETHER2 antibodymolecular imagingPARPpatient–derived xenografttargeted therapy

Identifiers

PMID37626587
PMCPMC10452700
OpenAlexW4385277857

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.