Evidence map›Paper›PMID 36430490›Full record

ReviewInternational journal of molecular sciences2022

The Oncopig as an Emerging Model to Investigate Copper Regulation in Cancer.

Alyssa L Carlson, Jaime Carrazco-Carrillo, Aaron Loder, Lobna Elkhadragy, Kyle M Schachtschneider, Teresita Padilla-Benavides

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. 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
0.5field-weighted citation impact, top 41% 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, 4 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

6 authors at 3 institutions in 1 country.

Alyssa L CarlsonDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.ORCID 0000-0002-4347-0278
Jaime Carrazco-CarrilloDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.
Aaron LoderDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.
Lobna ElkhadragyDepartment of Radiology, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0001-8956-298X
Kyle M SchachtschneiderDepartment of Radiology, University of Illinois at Chicago, Chicago, IL 60607, USA.
Teresita Padilla-BenavidesDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.ORCID 0000-0002-4624-0822
Wesleyan University · USUniversity of Illinois Chicago · USUniversity of Illinois Urbana-Champaign · US

Funding

Mechanisms of Cu-binding factors to promote myogenic gene expressionR01AR077578 · NIAMS · WESLEYAN UNIVERSITY · PI Teresita Del Nino Jesus Padilla-Benavides · 2021 to 2026
$2.1M
NIAMS NIH HHS R01 AR077578NIH HHS R01AR077578
6 · The paper itself

Abstract

Emerging evidence points to several fundamental contributions that copper (Cu) has to promote the development of human pathologies such as cancer. These recent and increasing identification of the roles of Cu in cancer biology highlights a promising field in the development of novel strategies against cancer. Cu and its network of regulatory proteins are involved in many different contextual aspects of cancer from driving cell signaling, modulating cell cycle progression, establishing the epithelial-mesenchymal transition, and promoting tumor growth and metastasis. Human cancer research in general requires refined models to bridge the gap between basic science research and meaningful clinical trials. Classic studies in cultured cancer cell lines and animal models such as mice and rats often present caveats when extended to humans due to inherent genetic and physiological differences. However, larger animal models such as pigs are emerging as more appropriate tools for translational research as they present more similarities with humans in terms of genetics, anatomical structures, organ sizes, and pathological manifestations of diseases like cancer. These similarities make porcine models well-suited for addressing long standing questions in cancer biology as well as in the arena of novel drug and therapeutic development against human cancers. With the emergent roles of Cu in human health and pathology, the pig presents an emerging and valuable model to further investigate the contributions of this metal to human cancers. The Oncopig Cancer Model is a transgenic swine model that recapitulates human cancer through development of site and cell specific tumors. In this review, we briefly outline the relationship between Cu and cancer, and how the novel Oncopig Cancer Model may be used to provide a better understanding of the mechanisms and causal relationships between Cu and molecular targets involved in cancer.

Indexed as

CopperNeoplasmsAnimalsHumansMiceRatsSwineTranslational Research, BiomedicalCoppercoppercuproproteinshomeostasismetal transportOncopig

Identifiers

PMID36430490
PMCPMC9697225
OpenAlexW4309007667

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.