Evidence map›Paper›PMID 37064130›Full record

ArticleFrontiers in oncology2023

A recombinant adenovirus vector containing the

Ruhan A, Naoto Kunimura, Shoko Tominaga, Erika Hirata, Shunya Nishioka, Misato Uesugi, Rion Yamazaki, Hideto Ueki, Koichi Kitagawa, Masato Fujisawa and 1 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 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
–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

3 citing papers in PubMed.

  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

11 authors.

Ruhan ADepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Naoto KunimuraDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Shoko TominagaDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Erika HirataDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Shunya NishiokaDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Misato UesugiDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Rion YamazakiDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Hideto UekiDivision of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.
Koichi KitagawaDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.
Masato FujisawaDivision of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.
Toshiro ShirakawaDepartment of Advanced Medical Science, Kobe University Graduate School of Science, Technology and Innovation, Kobe, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is known as the most difficult molecular subtype of breast cancer to treat. Recent studies revealed that cancer stem cells (CSCs) play a critical role in TNBC recurrence and metastasis. In this study, we developed a recombinant replication-deficient adenoviral vector (Ad-CD44-N-HIF-3α4), which contains a gene encoding a synthetic Notch (synNotch) receptor composed of the extracellular domain of CD44 (CD44-ECD) and the hypoxia-inducible factor (HIF)-3α4 connected by the Notch core regulatory region. CD44 is a transmembrane glycoprotein and known as a CSC marker in breast cancer and other malignancies. HIF-3α4 is a dominant-negative regulator of HIF-1α and HIF-2α and inhibits hypoxia-inducing effect. Both CD44 and HIF signals contribute cancer stemness and maintaining CSCs in breast cancer. The CD44-ECD in the synNotch receptor acts as the CD44 decoy receptor, and after a ligand such as a hyaluronic acid binds to the CD44-ECD, HIF-3α4 is released from the Notch core domain. We performed an

Indexed as

adenovirusbreast cancercancer stem cellsgene therapyHIF

Identifiers

PMID37064130
PMCPMC10090503

What OpenQuestion holds

Textmetadata
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.