Evidence map›Paper›PMID 20505744›Full record

ArticleThe Journal of investigative dermatology2010

The glutamate release inhibitor Riluzole decreases migration, invasion, and proliferation of melanoma cells.

Maithao N Le, Joseph L-K Chan, Stephen A Rosenberg, Adam S Nabatian, Kim T Merrigan, Karine A Cohen-Solal, James S Goydos

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.0field-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

43 citing papers in PubMed, 65 citations in OpenAlex.

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  6. ACell reports. Medicine · 2023
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  16. Antitumor Activity and Mechanism Study of Riluzole and Its Derivatives.Iranian journal of pharmaceutical research : IJPR · 2020
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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

7 authors at 2 institutions in 1 country.

Maithao N LeDivision of Surgical Oncology, Department of Surgery, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Joseph L-K Chan
Stephen A Rosenberg
Adam S Nabatian
Kim T Merrigan
Karine A Cohen-Solal
James S Goydos
Johnson University · USCancer Institute of Florida · US

Funding

Validation of Grm1 as a Therapeutic Target in MelanomaR01CA124975 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GOYDOS, JAMES S. · 2007 to 2011
$1.9M
Combination Therapy that Targets Glutamate Signaling in MelanomaR01CA149627 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GOYDOS, JAMES S. · 2010 to 2014
$1.7M
NCI NIH HHS R01 CA124975NCI NIH HHS R01CA124975NCI NIH HHS R01 CA149627
6 · The paper itself

Abstract

The goal of this study was to examine the effects of metabotropic glutamate receptor-1 (GRM1) blockade on melanoma anchorage-independent growth and invasion. We performed colony and invasion assays using GRM1-expressing melanoma lines and the GRM1-negative UACC930 line. Using the glutamate-release inhibitor Riluzole or the non-competitive GRM1 antagonist BAY 36-7620 we were able to induce considerable inhibition of colony formation and invasion in GRM1-expressing melanoma lines. Neither pharmacological agent induced significant reduction in colony formation or invasion in the GRM1-negative melanoma line, UACC930. Additionally we assessed the efficacy of these inhibitors to inhibit the growth of fresh melanoma tumor samples cultured on a 74-mum nylon mesh. Both Riluzole and BAY 36-7620 significantly inhibited tumor cell growth into the interstitial spaces of the mesh. When repeated with normal mole samples both inhibitors were much less effective in preventing the outgrowth of cells. These experiments show that a specific antagonist of GRM1 (BAY 36-7620) or an inhibitor of glutamate release (Riluzole) can significantly suppress melanoma migration, invasion and colony formation as well as inhibit the proliferation of fresh melanoma cells. These findings, added to our previous work, strengthen the case that GRM1 is a valid therapeutic target in patients with melanoma.

Indexed as

Cell DivisionCell Line, TumorCell MovementExcitatory Amino Acid AntagonistsExtracellular Signal-Regulated MAP KinasesGlutamic AcidHumansMelanomaNaphthalenesNeoplasm InvasivenessOrgan Culture TechniquesPhosphorylationProto-Oncogene Proteins c-aktReceptors, Metabotropic GlutamateRiluzoleSignal TransductionBAY36-7620Excitatory Amino Acid AntagonistsExtracellular Signal-Regulated MAP KinasesGlutamic Acidmetabotropic glutamate receptor type 1NaphthalenesProto-Oncogene Proteins c-aktReceptors, Metabotropic GlutamateRiluzole

Identifiers

PMID20505744
PMCPMC4004181
OpenAlexW2087678487

What OpenQuestion holds

Textmetadata
LicenceTDM
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.