Evidence map›Paper›PMID 29976975›Full record

ArticleOncogenesis2018

FOXC1 plays a crucial role in the growth of pancreatic cancer.

Ramadevi Subramani, Fernando A Camacho, Carly Ivy Levin, Kristina Flores, Alexa Clift, Adriana Galvez, Mauricio Terres, Servando Rivera, Sai Navana Kolli, Joshua Dodderer and 5 more

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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  18. The Dominant Role of Forkhead Box Proteins in Cancer.International journal of molecular sciences · 2018
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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

15 authors at 2 institutions in 1 country.

Ramadevi SubramaniCenter of Emphasis in Cancer Research, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.ORCID http://orcid.org/0000-0002-1054-0903
Fernando A CamachoGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Carly Ivy LevinGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Kristina FloresGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Alexa CliftGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Adriana GalvezCenter of Emphasis in Cancer Research, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Mauricio TerresThe University of Texas at El Paso, El Paso, TX, 79968, USA.
Servando RiveraGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Sai Navana KolliThe University of Texas at El Paso, El Paso, TX, 79968, USA.
Joshua DoddererCenter of Emphasis in Cancer Research, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Megan MirandaThe University of Texas at El Paso, El Paso, TX, 79968, USA.
Alejandro RodriguezThe University of Texas at El Paso, El Paso, TX, 79968, USA.
Diego A PedrozaGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Animesh ChatterjeeCenter of Emphasis in Cancer Research, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA.
Rajkumar LakshmanaswamyCenter of Emphasis in Cancer Research, Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, 79905, USA. rajkumar.lakshmanaswamy@ttuhsc.edu.
Texas Tech University · USThe University of Texas at El Paso · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IGF-1R signaling controls various vital cellular functions and this signaling is deregulated in many cancers, including pancreatic cancer. Several efforts have mainly focused on inhibiting the IGF-1R signaling cascade. The outcomes of these focused preclinical studies have been positive, whereas clinical trials of IGF-1R inhibitors in pancreatic cancer have failed, raising the questions about this therapeutic approach. This necessitates a better understanding of the role of IGF-1R signaling in pancreatic cancer. We investigated the impact of IGF-1R signaling on crucial transcription factors and identified the FOXC1 as one of the crucial regulator of IGF-1R signaling. We employed genetic approaches to overexpress and silence FOXC1 in pancreatic cancer cells. Our results demonstrate that IGF-1R and FOXC1 seem to positively regulate each other. Further, FOXC1 increased the metastatic abilities of pancreatic cancer cells by enhancing cell proliferation, migration, invasion, epithelial-to-mesenchymal transition, and angiogenesis. The data from xenograft experiments further established the importance of FOXC1 in pancreatic tumorigenesis. In conclusion, FOXC1 is a potent oncogenic transcription factor, which promotes pancreatic cancer growth and metastasis. Thus, targeting FOXC1 could be a potential therapeutic strategy against pancreatic cancer.

Identifiers

PMID29976975
PMCPMC6033944
OpenAlexW2810797281

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.