Measurement of 45 cytokine, chemokine and growth factors in established cell culture supernatants and autologous serum from advanced melanoma patients.


Journal

Carcinogenesis
ISSN: 1460-2180
Titre abrégé: Carcinogenesis
Pays: England
ID NLM: 8008055

Informations de publication

Date de publication:
28 05 2021
Historique:
received: 06 06 2020
revised: 31 12 2020
accepted: 08 01 2021
pubmed: 10 1 2021
medline: 30 9 2021
entrez: 9 1 2021
Statut: ppublish

Résumé

Melanoma is one of the most aggressive forms of human cancer and its incidence has significantly increased worldwide over the last decades. This neoplasia has been characterized by the release of a wide variety of soluble factors, which could stimulate tumor cell proliferation and survival in an autocrine and paracrine manner. Consequently, we sought to evaluate the pattern of soluble factors produced by pre-metastatic and metastatic melanoma established cultures, and to determine whether these factors can be detected in the autologous serum of malignant melanoma patients. Our results showed that both melanoma cultures had a common profile of 27 soluble factors mainly characterized by the high expression of VEGF-A, IL-6, MCP-1, IL-8, and SDF-1. In addition, when we compared supernatants, we observed significant differences in VEGF-A, BDNF, FGF-2, and NGF-β concentrations. As we found in melanoma cultures, serum samples also had their specific production pattern composed by 21 soluble factors. Surprisingly, PDGF-BB and EGF were only found in serum, whereas IL-2, IL-4, IL-8, IL31, FGF2, and GRO-α were only expressed in the supernatant. Significant differences in PDGF-BB, MIP-1β, HGF, PIGF-1, BDNF, EGF, Eotaxin, and IP-10 were also found after comparing autologous serum with healthy controls. According to this, no correlation was found between culture supernatants and autologous serum samples, which suggests that some factors may act locally, and others systemically. Nonetheless, after validation of our results in an independent cohort of patients, we concluded that PDGF-BB, VEGF-A, and IP-10 serum levels could be used to monitor different melanoma stages.

Identifiants

pubmed: 33421057
pii: 6076259
doi: 10.1093/carcin/bgab004
doi:

Substances chimiques

CCL2 protein, human 0
CXCL10 protein, human 0
CXCL12 protein, human 0
Chemokine CCL2 0
Chemokine CXCL10 0
Chemokine CXCL12 0
Cytokines 0
Interleukin-6 0
Interleukin-8 0
Neoplasm Proteins 0
Vascular Endothelial Growth Factor A 0
Becaplermin 1B56C968OA

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

714-723

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Yoel Genaro Montoyo-Pujol (YG)

Servicio de Inmunología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Laboratorio de Apoyo a la Investigación, Hospital General Universitario de Alicante e Instituto de Investigación Sanitaria y Biomédica de Alicante (ISABIAL), Alicante, Spain.

Xu Wang (X)

Servicio de Inmunología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Programa de doctorado en Biomedicina, Universidad de Granada, Granada, Spain.

Sandra Bermúdez-Sánchez (S)

Servicio de Inmunología, Hospital Universitario Virgen de las Nieves, Granada, Spain.

Aurelio Martin (A)

Servicio de Anatomía Patológica, Hospital Universitario Virgen de las Nieves, Granada, Spain.

Francisco Almazan (F)

Servicio de Dermatología, Hospital Clínico Universitario San Cecilio, Granada, Spain.

Miguel Ángel López-Nevot (MÁ)

Servicio de Inmunología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Departamento Bioquímica, Biología Molecular e Inmunología III, Facultad de Medicina, Universidad de Granada. Avda. de la Investigación, Granada, Spain.
Instituto de Investigación Biosanitaria I, Granada, Spain.

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Classifications MeSH