Evidence map›Paper›PMID 33469705›Full record

ArticleCellular and molecular life sciences : CMLS2021

MACC1 regulates clathrin-mediated endocytosis and receptor recycling of transferrin receptor and EGFR in colorectal cancer.

Francesca Imbastari, Mathias Dahlmann, Anje Sporbert, Camilla Ciolli Mattioli, Tommaso Mari, Florian Scholz, Lena Timm, Shailey Twamley, Rebekka Migotti, Wolfgang Walther and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Francesca ImbastariTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany.ORCID http://orcid.org/0000-0001-8440-9847
Mathias DahlmannTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany. dahlmann@mdc-berlin.de.ORCID http://orcid.org/0000-0002-0036-5283
Anje SporbertAdvanced Light Microscopy, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.ORCID http://orcid.org/0000-0002-3738-1295
Camilla Ciolli MattioliBerlin Institute for Medical Systems Biology, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.ORCID http://orcid.org/0000-0002-8499-1387
Tommaso MariProteome Dynamics, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.ORCID http://orcid.org/0000-0001-6011-9386
Florian ScholzTumor Immunology, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
Lena TimmTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany.
Shailey TwamleyTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany.
Rebekka MigottiMax-Delbrück-Center for Molecular Medicine, Berlin, Germany.
Wolfgang WaltherTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany.ORCID http://orcid.org/0000-0003-2884-0231
Gunnar DittmarProteomics of Cellular Signaling, Luxembourg Institute of Health, Strassen, Luxembourg.ORCID http://orcid.org/0000-0003-3647-8623
Armin RehmTumor Immunology, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
Ulrike SteinTranslational Oncology of Solid Tumors, Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine Berlin in the Helmholtz-Association, Robert-Rössle-Straße 10, 13125, Berlin, Germany. ustein@mdc-berlin.de.ORCID http://orcid.org/0000-0001-7006-282X
Max Delbrück Center · DEGerman Cancer Research Center · DELuxembourg Institute of Health · LU

Funding

German Cancer Consortium DKTK
6 · The paper itself

Abstract

Metastasis Associated in Colon Cancer 1 (MACC1) is a novel prognostic, predictive and causal biomarker for tumor progression and metastasis in many cancer types, including colorectal cancer. Besides its clinical value, little is known about its molecular function. Its similarity to SH3BP4, involved in regulating uptake and recycling of transmembrane receptors, suggests a role of MACC1 in endocytosis. By exploring the MACC1 interactome, we identified the clathrin-mediated endocytosis (CME)-associated proteins CLTC, DNM2 and AP-2 as MACC1 binding partners. We unveiled a MACC1-dependent routing of internalized transferrin receptor towards recycling. Elevated MACC1 expression caused also the activation and internalization of EGFR, a higher rate of receptor recycling, as well as earlier and stronger receptor activation and downstream signaling. These effects are limited by deletion of CME-related protein interaction sites in MACC1. Thus, MACC1 regulates CME and receptor recycling, causing increased growth factor-mediated downstream signaling and cell proliferation. This novel mechanism unveils potential therapeutic intervention points restricting MACC1-driven metastasis.

Indexed as

EndocytosisGene Expression Regulation, NeoplasticAnimalsApoptosisBiomarkers, TumorCell ProliferationClathrinColorectal NeoplasmsErbB ReceptorsHumansMiceProteomeReceptors, TransferrinTrans-ActivatorsTumor Cells, CulturedXenograft Model Antitumor AssaysBiomarkers, TumorClathrinEGFR protein, humanErbB ReceptorsMACC1 protein, humanProteomeReceptors, TransferrinTrans-ActivatorsCMEColorectal cancerEGFRMACC1Receptor recyclingTransferrin receptor

Identifiers

PMID33469705
PMCPMC8038998
OpenAlexW3125974259

What OpenQuestion holds

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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.