Karachaliou Niki, Pilotto Sara, Teixidó Cristina, Viteri Santiago, González-Cao María, Riso Aldo, Morales-Espinosa Daniela, Molina Miguel Angel, Chaib Imane, Santarpia Mariacarmela, Richardet Eduardo, Bria Emilio, Rosell Rafael
1 Instituto Oncológico Dr Rosell, Quiron-Dexeus University Hospital, Barcelona, Spain ; 2 Department of Medical Oncology, University of Verona, Azienda Ospedaliera Universitaria Integrata, Verona, Italy ; 3 Pangaea Biotech, Quirón Dexeus University Institute, Barcelona, Spain ; 4 Catalan Institute of Oncology, Hospital Germans Trias i Pujol, Badalona, Spain ; 5 Medical Oncology Unit, Human Pathology Department, University of Messina, Messina 98122, Italy ; 6 Instituto Oncológico de Córdoba, Córdoba, Argentina ; 7 Molecular Oncology Research (MORe) Foundation, Barcelona, Spain ; 8 Germans Trias i Pujol Health Sciences Institute and Hospital, Campus Can Ruti, Barcelona, Spain.
Ann Transl Med. 2015 Oct;3(18):265. doi: 10.3978/j.issn.2305-5839.2015.08.06.
Advances and in-depth understanding of the biology of melanoma over the past 30 years have contributed to a change in the consideration of melanoma as one of the most therapy-resistant malignancies. The finding that oncogenic BRAF mutations drive tumor growth in up to 50% of melanomas led to a molecular therapy revolution for unresectable and metastatic disease. Moving beyond BRAF, inactivation of immune regulatory checkpoints that limit T cell responses to melanoma has provided targets for cancer immunotherapy. In this review, we discuss the molecular biology of melanoma and we focus on the recent advances of molecularly targeted and immunotherapeutic approaches.
在过去30年里,黑色素瘤生物学的进展和深入理解促使人们对黑色素瘤的认识发生了变化,不再将其视为最具治疗抗性的恶性肿瘤之一。致癌性BRAF突变在高达50%的黑色素瘤中驱动肿瘤生长,这一发现引发了针对不可切除和转移性疾病的分子治疗革命。除了BRAF之外,限制T细胞对黑色素瘤反应的免疫调节检查点的失活为癌症免疫治疗提供了靶点。在本综述中,我们讨论了黑色素瘤的分子生物学,并重点关注分子靶向和免疫治疗方法的最新进展。