Evidence map›Paper›PMID 30841571›Full record

ReviewCancers2019

The Role of M3 Muscarinic Receptor Ligand-Induced Kinase Signaling in Colon Cancer Progression.

Mazen Tolaymat, Shannon M Larabee, Shien Hu, Guofeng Xie, Jean-Pierre Raufman

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  15. Sympathetic and parasympathetic innervation in cancer: therapeutic implications.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2021
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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

5 authors at 1 institution in 1 country.

Mazen TolaymatDepartment of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA. mazentolaymat@umm.edu.
Shannon M LarabeeDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA. slarabee@som.umaryland.edu.ORCID 0000-0003-4308-3099
Shien HuDepartment of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA. shu1@som.umaryland.edu.
Guofeng XieDepartment of Medicine, University of Maryland School of Medicine and VA Maryland Health Care System, Baltimore, MD 21201, USA. gxie@som.umaryland.edu.
Jean-Pierre RaufmanDepartment of Medicine, University of Maryland School of Medicine and VA Maryland Health Care System, Baltimore, MD 21201, USA. jraufman@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

Research Training in Gastroenterology and HepatologyT32DK067872 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI RAUFMAN, JEAN-PIERRE · 2005 to 2024
$7.2M
Transcriptional Repression of MMP7 by FXR in Intestinal Epithelial CellsI01BX002777 · VA · BALTIMORE VA MEDICAL CENTER · PI XIE, GUOFENG · 2016 to 2020
–
Biomedical Laboratory Research and Development, VA Office of Research and Development BX002129, BX002777BLRD VA I01 BX002777National Institutes of Health DK067872NIDDK NIH HHS T32 DK067872
6 · The paper itself

Abstract

Despite a reduction in incidence over the past decade, colon cancer remains the second most common cause of cancer death in the United States; recent demographics suggest this disease is now afflicting younger persons. M₃ muscarinic receptor (M₃R) mRNA and protein are over-expressed in colon cancer, and M₃R can be activated by both traditional (e.g., acetylcholine) and non-traditional (e.g., bile acids) muscarinic ligands. In this review, we weigh the data supporting a prominent role for key protein kinases downstream of M₃R activation in promoting colon cancer progression and dissemination. Specifically, we explore the roles that downstream activation of the mitogen activated protein kinase/extracellular signal-related kinase (MAPK/ERK), protein kinase C, p38 MAPK, and phosphatidylinositol 3-kinase/Akt (PI3K/Akt) pathways play in mediating colon cancer cell proliferation, survival, migration and invasion. We assess the impact of M₃R-stimulated induction of selected matrix metalloproteinases germane to these hallmarks of colon cancer progression. In this context, we also critically review the reproducibility of findings derived from a variety of in vivo and in vitro colon cancer models, and their fidelity to human disease. Finally, we summarize the therapeutic potential of targeting various steps from ligand-M₃R interaction to the activation of key downstream molecules.

Indexed as

acetylcholinebile acidscolon cancermuscarinic ligandsmuscarinic receptors

Identifiers

PMID30841571
PMCPMC6468573
OpenAlexW2919448754

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.