Evidence map›Paper›PMID 38675909›Full record

ArticleViruses2024

Oncolytic Adenovirus for the Targeting of Paclitaxel-Resistant Breast Cancer Stem Cells.

Sacha Robert, Natasha Ivelisse Roman Ortiz, Christopher J LaRocca, Julie Hanson Ostrander, Julia Davydova

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2024. 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
3.3field-weighted citation impact, top 8% 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, 6 citations in OpenAlex.

  1. Review
  2. Review
  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

5 authors at 1 institution in 1 country.

Sacha RobertDepartment of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-2807-4410
Natasha Ivelisse Roman OrtizDepartment of Pharmacology, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-4348-6165
Christopher J LaRoccaDepartment of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-9808-1405
Julie Hanson OstranderMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0002-5038-6875
Julia DavydovaDepartment of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.
University of Minnesota · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UM1TR004405 · NCATS · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar, Damien A Fair · 2023 to 2026
$30.8M
CTSA K12 Program at University of MinnesotaK12TR004373 · NCATS · UNIVERSITY OF MINNESOTA · PI David H Ingbar · 2024 to 2026
$3.2M
SRC-3/PELP1 complexes drive stem-like phenotypes in luminal breast cancerR01CA236948 · NCI · UNIVERSITY OF MINNESOTA · PI LANGE, CAROL A, OSTRANDER, JULIE H · 2020 to 2024
$2.4M
Advancing Systematic Delivery of Oncolytic Adenovirus for Pancreatic CancerR01CA276179 · NCI · UNIVERSITY OF MINNESOTA · PI Julia Davydova · 2023 to 2026
$2.0M
Combination therapy with IFN expressing oncolytic adenovirus for pancreatic cancerR01CA228760 · NCI · UNIVERSITY OF MINNESOTA · PI DAVYDOVA, JULIA, YAMAMOTO, MASATO · 2019 to 2023
$1.7M
Novel Theranostics for Pancreatic CancerR01CA174861 · NCI · UNIVERSITY OF MINNESOTA · PI DAVYDOVA, JULIA · 2014 to 2018
$1.6M
NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA174861NCI NIH HHS R01 CA228760NCI NIH HHS R01 CA236948NCI NIH HHS R01 CA276179NIH HHS R01CA174861NIH HHS R01CA228760NIH HHS R01CA236948NIH HHS R01CA276179
6 · The paper itself

Abstract

Adjuvant systemic therapies effectively reduce the risk of breast cancer recurrence and metastasis, but therapy resistance can develop in some patients due to breast cancer stem cells (BCSCs). Oncolytic adenovirus (OAd) represents a promising therapeutic approach as it can specifically target cancer cells. However, its potential to target BCSCs remains unclear. Here, we evaluated a Cox-2 promoter-controlled, Ad5/3 fiber-modified OAd designed to encode the human sodium iodide symporter (hNIS) in breast cancer models. To confirm the potential of OAds to target BCSCs, we employed BCSC-enriched estrogen receptor-positive (ER+) paclitaxel-resistant (TaxR) cells and tumorsphere assays. OAd-hNIS demonstrated significantly enhanced binding and superior oncolysis in breast cancer cells, including ER+ cells, while exhibiting no activity in normal mammary epithelial cells. We observed improved NIS expression as the result of adenovirus death protein deletion. OAd-hNIS demonstrated efficacy in targeting TaxR BCSCs, exhibiting superior killing and hNIS expression compared to the parental cells. Our vector was capable of inhibiting tumorsphere formation upon early infection and reversing paclitaxel resistance in TaxR cells. Importantly, OAd-hNIS also destroyed already formed tumorspheres seven days after their initiation. Overall, our findings highlight the promise of OAd-hNIS as a potential tool for studying and targeting ER+ breast cancer recurrence and metastasis.

Indexed as

AdenoviridaeBreast NeoplasmsDrug Resistance, NeoplasmNeoplastic Stem CellsOncolytic VirotherapyOncolytic VirusesPaclitaxelAnimalsCell Line, TumorFemaleGenetic VectorsHumansMiceSodium-Iodide SymportersSymportersPaclitaxelSodium-Iodide SymportersSymportersbreast cancerbreast cancer stem cellchemoresistancehuman adenovirusoncolytic vectorssodium iodide symporter

Identifiers

PMID38675909
PMCPMC11054319
OpenAlexW4393993343

What Socratic 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 Socratic graph.