Evidence map›Paper›PMID 34638342›Full record

ArticleCancers2021

CD147 Promotes Tumor Lymphangiogenesis in Melanoma via PROX-1.

Coralie Reger de Moura, Alexandra Landras, Farah Khayati, Uwe Maskos, Kamel Maouche, Maxime Battistella, Suzanne Menashi, Céleste Lebbé, Samia Mourah

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 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

9 authors at 5 institutions in 1 country.

Coralie Reger de MouraInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Alexandra LandrasInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Farah KhayatiInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Uwe MaskosNeurobiologie Intégrative des Systèmes Cholinergiques, Institut Pasteur, Université de Paris, CNRS, UMR_3571, 75724 Paris, France.
Kamel MaoucheBiology and Pathology of the Endocrine Pancreas, Université de Paris, CNRS, UMR_8251, 75013 Paris, France.
Maxime BattistellaInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Suzanne MenashiPharmacogenomics Department, Saint Louis Hospital, AP-HP, 75010 Paris, France.
Céleste LebbéInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Samia MourahInserm, UMR_S976, Université de Paris, 75010 Paris, France.
Hôpital Saint-Louis · FRInserm · FRUniversité Paris Cité · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma is one of the most aggressive skin cancers and is characterized by early lymph node metastasis and the capacity to develop resistance to therapies. Hence, understanding the regulation of lymphangiogenesis through mechanisms contributing to lymphatic vessel formation represents a treatment strategy for metastatic cancer. We have previously shown that CD147, a transmembrane glycoprotein overexpressed in melanoma, regulates the angiogenic process in endothelial cells. In this study, we show a correlation between high CD147 expression levels and the number of lymphatic vessels expressing LYVE-1, Podoplanin, and VEGFR-3 in human melanoma lymph nodes. CD147 upregulates in vitro lymphangiogenesis and its related mediators through the PROX-1 transcription factor. In vivo studies in a melanoma model confirmed that CD147 is involved in metastasis through a similar mechanism as in vitro. This study, demonstrating the paracrine role of CD147 in the lymphangiogenesis process, suggests that CD147 could be a promising target for the inhibition of melanoma-associated lymphangiogenesis.

Indexed as

CD147lymphangiogenesislymph node metastasismelanomatherapeutic targets

Identifiers

PMID34638342
PMCPMC8508014
OpenAlexW3203790717

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.