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


Por: Montoyo-Pujol, Y, Wang, X, Bermudez-Sanchez, S, Martin, A, Almazan, F and Lopez-Nevot, M

Publicada: 1 may 2021 Ahead of Print: 1 ene 2021
Resumen:
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-beta 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-alpha were only expressed in the supernatant. Significant differences in PDGF-BB, MIP-1 beta, 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.

Filiaciones:
:
 Hosp Univ Virgen de las Nieves, Serv Inmunol, Avda Fuerzas Armadas S-N, Granada 18014, Spain

 Hosp Gen Univ Alicante, Lab Apoyo Invest, Pintor Baeza 12, Alicante 03010, Spain

 Inst Invest Sanitaria & Biomed Alicante ISABIAL, Pintor Baeza 12, Alicante 03010, Spain

Wang, X:
 Hosp Univ Virgen de las Nieves, Serv Inmunol, Avda Fuerzas Armadas S-N, Granada 18014, Spain

 Univ Granada, Programa Doctorado Biomed, Avda Madrid 13, Granada 18071, Spain

Bermudez-Sanchez, S:
 Hosp Univ Virgen de las Nieves, Serv Inmunol, Avda Fuerzas Armadas S-N, Granada 18014, Spain

Martin, A:
 Hosp Univ Virgen de las Nieves, Serv Anat Patol, Avda Fuerzas Armadas S-N, Granada 18014, Spain

Almazan, F:
 Hosp Clin Univ San Cecilio, Serv Dermatol, Avda Conocimiento S-N, Granada 18016, Spain

Lopez-Nevot, M:
 Hosp Univ Virgen de las Nieves, Serv Inmunol, Avda Fuerzas Armadas S-N, Granada 18014, Spain

 Univ Granada, Dept Bioquim Biol Mol & Inmunol 3, Fac Med, Avda Invest 11, Granada 18016, Spain

 Ibs GRANADA, Inst Invest Biosanitaria I, Avda Fuerzas Armadas 2, Granada 18014, Spain
ISSN: 01433334
Editorial
OXFORD UNIV PRESS, England, Reino Unido
Tipo de documento: Article
Volumen: 42 Número: 5
Páginas: 714-723
WOS Id: 000661465600006
ID de PubMed: 33421057

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