Pardella Elisa, Pranzini Erica, Leo Angela, Taddei Maria Letizia, Paoli Paolo, Raugei Giovanni
Department of Experimental and Clinical Biomedical Sciences "Mario Serio" University of Florence, Viale Morgagni 50, 50134 Florence, Italy.
Department of Experimental and Clinical Medicine, University of Florence, Viale Morgagni 50, 50134 Florence, Italy.
Cancers (Basel). 2020 Sep 29;12(10):2799. doi: 10.3390/cancers12102799.
Despite a large number of therapeutic options available, malignant melanoma remains a highly fatal disease, especially in its metastatic forms. The oncogenic role of protein tyrosine phosphatases (PTPs) is becoming increasingly clear, paving the way for novel antitumor treatments based on their inhibition. In this review, we present the oncogenic PTPs contributing to melanoma progression and we provide, where available, a description of new inhibitory strategies designed against these enzymes and possibly useful in melanoma treatment. Considering the relevance of the immune infiltrate in supporting melanoma progression, we also focus on the role of PTPs in modulating immune cell activity, identifying interesting therapeutic options that may support the currently applied immunomodulating approaches. Collectively, this information highlights the value of going further in the development of new strategies targeting oncogenic PTPs to improve the efficacy of melanoma treatment.
尽管有大量可用的治疗选择,但恶性黑色素瘤仍然是一种高度致命的疾病,尤其是其转移性形式。蛋白酪氨酸磷酸酶(PTPs)的致癌作用越来越明显,为基于其抑制作用的新型抗肿瘤治疗铺平了道路。在本综述中,我们介绍了促成黑色素瘤进展的致癌PTPs,并在可行的情况下,描述针对这些酶设计的新抑制策略,这些策略可能对黑色素瘤治疗有用。考虑到免疫浸润在支持黑色素瘤进展中的相关性,我们还关注PTPs在调节免疫细胞活性中的作用,确定可能支持当前应用的免疫调节方法的有趣治疗选择。总体而言,这些信息突出了进一步开发针对致癌PTPs的新策略以提高黑色素瘤治疗效果的价值。