Evidence map›Paper›PMID 30290833›Full record

ArticleJournal of experimental & clinical cancer research : CR2018

Acidic microenvironment plays a key role in human melanoma progression through a sustained exosome mediated transfer of clinically relevant metastatic molecules.

Zaira Boussadia, Jessica Lamberti, Fabrizio Mattei, Elisabetta Pizzi, Rossella Puglisi, Cristiana Zanetti, Luca Pasquini, Federica Fratini, Luca Fantozzi, Federica Felicetti and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

99 citing papers in PubMed, 146 citations in OpenAlex.

  1. Review
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  3. Endogenous Engineering Reprograms Extracellular Vesicles for Enhanced Therapeutic Function.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  15. Local Exosome Inhibition Potentiates Mild Photothermal Immunotherapy Against Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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  19. The role of extracellular vesicle immune checkpoints in cancer.Clinical and experimental immunology · 2024
    Review
  20. Article

39 more citing papers are in PubMed but not listed here.

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

17 authors at 2 institutions in 1 country.

Zaira BoussadiaGlobal Health Center, Istituto Superiore di Sanità, Rome, Italy.
Jessica LambertiOncology and Molecular Medicine Department, Istituto Superiore di Sanità, Rome, Italy.
Fabrizio MatteiOncology and Molecular Medicine Department, Istituto Superiore di Sanità, Rome, Italy.
Elisabetta PizziMajor Equipments and Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Rossella PuglisiCenter for Gender- specific Medicine, Istituto Superiore di Sanità, Istituto Superiore di Sanità, Rome, Italy.
Cristiana ZanettiOncology and Molecular Medicine Department, Istituto Superiore di Sanità, Rome, Italy.
Luca PasquiniMajor Equipments and Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Federica FratiniMajor Equipments and Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Luca FantozziMajor Equipments and Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Federica FelicettiOncology and Molecular Medicine Department, Istituto Superiore di Sanità, Rome, Italy.
Katia FecchiGlobal Health Center, Istituto Superiore di Sanità, Rome, Italy.
Carla RaggiNational Center for the Control and Evaluation of Medicine, Istituto Superiore di Sanità, Rome, Italy.
Massimo SanchezMajor Equipments and Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Stefania D'AtriLaboratory of Molecular Oncology, Istituto Dermopatico dell'Immacolata- IRCCS, Rome, Italy.
Alessandra CarèCenter for Gender- specific Medicine, Istituto Superiore di Sanità, Istituto Superiore di Sanità, Rome, Italy.
Massimo SargiacomoGlobal Health Center, Istituto Superiore di Sanità, Rome, Italy.
Isabella ParoliniOncology and Molecular Medicine Department, Istituto Superiore di Sanità, Rome, Italy. isabella.parolini@iss.it.ORCID http://orcid.org/0000-0001-9863-1051
Istituto Superiore di Sanità · ITIstituto Dermopatico dell'Immacolata · IT

Funding

Ministero della Salute RF-2011-02347300
6 · The paper itself

Abstract

backgroundMicroenvironment cues involved in melanoma progression are largely unknown. Melanoma is highly influenced in its aggressive phenotype by the changes it determinates in its microenvironment, such as pH decrease, in turn influencing cancer cell invasiveness, progression and tissue remodelling through an abundant secretion of exosomes, dictating cancer strategy to the whole host. A role of exosomes in driving melanoma progression under microenvironmental acidity was never described.

methodsWe studied four differently staged human melanoma lines, reflecting melanoma progression, under microenvironmental acidic pHs pressure ranging between pH 6.0-6.7. To estimate exosome secretion as a function of tumor stage and environmental pH, we applied a technique to generate native fluorescent exosomes characterized by vesicles integrity, size, density, markers expression, and quantifiable by direct FACS analysis. Functional roles of exosomes were tested in migration and invasion tests. Then we performed a comparative proteomic analysis of acid versus control exosomes to elucidate a specific signature involved in melanoma progression.

resultsWe found that metastatic melanoma secretes a higher exosome amount than primary melanoma, and that acidic pH increases exosome secretion when melanoma is in an intermediate stage, i.e. metastatic non-invasive. We were thus able to show that acidic pH influences the intercellular cross-talk mediated by exosomes. In fact when exposed to exosomes produced in an acidic medium, pH naïve melanoma cells acquire migratory and invasive capacities likely due to transfer of metastatic exosomal proteins, favoring cell motility and angiogenesis. A Prognoscan-based meta-analysis study of proteins enriched in acidic exosomes, identified 11 genes (HRAS, GANAB, CFL2, HSP90B1, HSP90AB1, GSN, HSPA1L, NRAS, HSPA5, TIMP3, HYOU1), significantly correlating with poor prognosis, whose high expression was in part confirmed in bioptic samples of lymph node metastases.

conclusionsA crucial step of melanoma progression does occur at melanoma intermediate -stage, when extracellular acidic pH induces an abundant release and intra-tumoral uptake of exosomes. Such exosomes are endowed with pro-invasive molecules of clinical relevance, which may provide a signature of melanoma advancement.

Indexed as

Cell Line, TumorDisease ProgressionEndoplasmic Reticulum Chaperone BiPExosomesHumansMelanomaMicroscopy, ConfocalNeoplasm MetastasisTumor MicroenvironmentEndoplasmic Reticulum Chaperone BiPExosomesMelanoma progressionMicroenvironmental acidic pHTumor stage

Identifiers

PMID30290833
PMCPMC6173926
OpenAlexW2895043275

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.