Evidence map›Paper›PMID 32733880›Full record

ArticleFrontiers in cell and developmental biology2020

TRPM7/RPSA Complex Regulates Pancreatic Cancer Cell Migration.

Thibaut Lefebvre, Pierre Rybarczyk, Clara Bretaudeau, Alison Vanlaeys, Rémi Cousin, Sylvie Brassart-Pasco, Denis Chatelain, Isabelle Dhennin-Duthille, Halima Ouadid-Ahidouch, Bertrand Brassart and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

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  11. The Role of TRPM7 in Oncogenesis.International journal of molecular sciences · 2024
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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

11 authors at 3 institutions in 1 country.

Thibaut LefebvreLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Pierre RybarczykLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Clara BretaudeauUMR CNRS 7369 Matrice Extracellulaire et Dynamique Cellulaire (MEDyC), Université de Reims Champagne Ardenne (URCA), Reims, France.
Alison VanlaeysLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Rémi CousinUMR CNRS 7369 Matrice Extracellulaire et Dynamique Cellulaire (MEDyC), Université de Reims Champagne Ardenne (URCA), Reims, France.
Sylvie Brassart-PascoUMR CNRS 7369 Matrice Extracellulaire et Dynamique Cellulaire (MEDyC), Université de Reims Champagne Ardenne (URCA), Reims, France.
Denis ChatelainService d'Anatomie et Cytologie Pathologiques, CHU Amiens-Picardie, Amiens, France.
Isabelle Dhennin-DuthilleLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Halima Ouadid-AhidouchLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Bertrand BrassartUMR CNRS 7369 Matrice Extracellulaire et Dynamique Cellulaire (MEDyC), Université de Reims Champagne Ardenne (URCA), Reims, France.
Mathieu GautierLaboratoire de Physiologie Cellulaire et Moléculaire - UR-UPJV 4667, UFR Sciences, Université de Picardie Jules Verne (UPJV), Amiens, France.
Laboratoire de physiologie cellulaire et moléculaire · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire Amiens-Picardie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a malignancy with a very poor prognosis due to highly metastatic profile. Cell migration is an essential step of the metastatic cascade allowing cancer cells to spread toward target tissues. Recent studies strongly suggest that bioactive elastin peptides, also named elastokines or elastin-derived peptides (EDPs), are released in the extracellular microenvironment during tumoral remodeling of the stroma. EDPs stimulate cancer cell migration by interacting with their membrane receptor, ribosomal protein SA (RPSA). Others membrane proteins like ion channels are also involved in cancer cell migration. It has been recently shown that the transient receptor potential melastatin-related 7 (TRPM7) channel regulates PDAC cell migration and invasion. The objective of this work was to study the effect of EDPs on TRPM7 channel in human pancreatic cancer cells. We showed that EDPs promote MIA PaCa-2 cell migration using Boyden chamber assay. Cells transfected with a siRNA targeting TRPM7 were not able to migrate in response to EDPs indicating that TRPM7 regulated cell migration induced by these peptides. Moreover, EDPs were able to stimulate TRPM7 currents recorded by Patch-Clamp. Finally, we showed that TRPM7 channels and RPSA receptors are colocalized at the plasma membrane of human pancreatic cancer cells. Taken together, our data suggest that TRPM7/RPSA complex regulated human pancreatic cancer cell migration. This complex may be a promising therapeutic target in PDAC.

Indexed as

cell migrationelastin-derived peptidespancreatic ductal adenocarcinomaribosomal protein SAtransient receptor potential melastatin-related 7

Identifiers

PMID32733880
PMCPMC7360683
OpenAlexW3040123332

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.