Evidence map›Paper›PMID 34874595›Full record

ArticleCancer science2022

Epidermal growth factor/epidermal growth factor receptor signaling blockage inhibits tumor cell-derived exosome uptake by oral squamous cell carcinoma through macropinocytosis.

Eri Sasabe, Ayumi Tomomura, Hangyu Liu, Shinya Sento, Naoya Kitamura, Tetsuya Yamamoto

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-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

17 citing papers in PubMed, 34 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

6 authors at 1 institution in 1 country.

Eri SasabeDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.ORCID https://orcid.org/0000-0001-6865-1772
Ayumi TomomuraDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.
Hangyu LiuDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.
Shinya SentoDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.
Naoya KitamuraDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.
Tetsuya YamamotoDepartment of Oral and Maxillofacial Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.
Kōchi University · JP

Funding

Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan 16K11688
6 · The paper itself

Abstract

Various cell types secrete exosomes into their surrounding extracellular space, which consequently affect the function and activity of recipient cells. Numerous studies have showed that tumor cell-derived exosomes play important roles in tumor growth and progression. Although a variety of endocytic pathways are reportedly involved in the cellular uptake of exosomes, detailed mechanisms remain unknown. The present study demonstrated that treatment with recombinant epidermal growth factor (EGF) time- and dose-dependently promoted cellular uptake of oral squamous cell carcinoma (OSCC) cell-derived exosomes into OSCC cells themselves. Conversely, EGF receptor (EGFR) knockdown and treatment with EGFR inhibitors, including erlotinib and cetuximab, abrogated OSCC cell uptake of exosomes. The macropinocytosis inhibitor 5-(N-ethyl-N-isopropyl) amiloride (EIPA) blocked the effects of active EGF/EGFR signaling on uptake of OSCC cell-derived exosomes. These EGFR inhibitors also suppressed OSCC cell-derived exosome-induced proliferation, migration, invasion, stemness, and chemoresistance of OSCC cells. Taken together, the data presented herein suggest that EGFR inhibitors might inhibit the malignant potential of OSCC cells through direct inhibition of not only EGFR downstream signaling pathway but also cellular uptake of OSCC cell-derived exosomes through macropinocytosis.

Indexed as

PinocytosisCell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmEpidermal Growth FactorErbB ReceptorsExosomesHumansMouth NeoplasmsNeoplastic Stem CellsProtein Kinase InhibitorsSignal TransductionSquamous Cell Carcinoma of Head and NeckEGFR protein, humanEpidermal Growth FactorErbB ReceptorsProtein Kinase InhibitorsEGFEGFRexosomemacropinocytosisoral squamous cell carcinoma

Identifiers

PMID34874595
PMCPMC8819298
OpenAlexW4200321756

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.