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Targeting EGFR in melanoma - The sea of possibilities to overcome drug resistance.
Pastwinska, Joanna; Karas, Kaja; Karwaciak, Iwona; Ratajewski, Marcin.
Afiliação
  • Pastwinska J; Laboratory of Epigenetics, Institute of Medical Biology, Polish Academy of Sciences, 90-364 Lodz, Poland.
  • Karas K; Laboratory of Epigenetics, Institute of Medical Biology, Polish Academy of Sciences, 90-364 Lodz, Poland.
  • Karwaciak I; Laboratory of Epigenetics, Institute of Medical Biology, Polish Academy of Sciences, 90-364 Lodz, Poland.
  • Ratajewski M; Laboratory of Epigenetics, Institute of Medical Biology, Polish Academy of Sciences, 90-364 Lodz, Poland. Electronic address: mratajewski@cbm.pan.pl.
Biochim Biophys Acta Rev Cancer ; 1877(4): 188754, 2022 07.
Article em En | MEDLINE | ID: mdl-35772580
Melanoma is considered one of the most aggressive skin cancers. It spreads and metastasizes quickly and is intrinsically resistant to most conventional chemotherapeutics, thereby presenting a challenge to researchers and clinicians searching for effective therapeutic strategies to treat patients with melanoma. The use of inhibitors of mutated serine/threonine-protein kinase B-RAF (BRAF), e.g., vemurafenib and dabrafenib, has revolutionized melanoma chemotherapy. Unfortunately, the response to these drugs lasts a limited time due to the development of acquired resistance. One of the proteins responsible for this process is epidermal growth factor receptor (EGFR). In this review, we summarize the role of EGFR signaling in the multidrug resistance of melanomas and discuss possible applications of EGFR inhibitors to overcome the development of drug resistance in melanoma cells during therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores ErbB / Melanoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores ErbB / Melanoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article