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      Sex and Gender Disparities in Melanoma

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          Abstract

          Worldwide, the total incidence of cutaneous melanoma is higher in men than in women, with some differences related to ethnicity and age and, above all, sex and gender. Differences exist in respect to the anatomic localization of melanoma, in that it is more frequent on the trunk in men and on the lower limbs in women. A debated issue is if—and to what extent—melanoma development can be attributed to gender-specific behaviors or to biologically intrinsic differences. In the search for factors responsible for the divergences, a pivotal role of sex hormones has been observed, although conflicting results indicate the involvement of other mechanisms. The presence on the X chromosome of numerous miRNAs and coding genes playing immunological roles represents another important factor, whose relevance can be even increased by the incomplete X chromosome random inactivation. Considering the known advantages of the female immune system, a different cancer immune surveillance efficacy was suggested to explain some sex disparities. Indeed, the complexity of this picture emerged when the recently developed immunotherapies unexpectedly showed better improvements in men than in women. Altogether, these data support the necessity of further studies, which consider enrolling a balanced number of men and women in clinical trials to better understand the differences and obtain actual gender-equitable healthcare.

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          Five-Year Outcomes with Dabrafenib plus Trametinib in Metastatic Melanoma

          Patients who have unresectable or metastatic melanoma with a BRAF V600E or V600K mutation have prolonged progression-free survival and overall survival when receiving treatment with BRAF inhibitors plus MEK inhibitors. However, long-term clinical outcomes in these patients remain undefined. To determine 5-year survival rates and clinical characteristics of the patients with durable benefit, we sought to review long-term data from randomized trials of combination therapy with BRAF and MEK inhibitors.
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            Cancer immunotherapy efficacy and patients' sex: a systematic review and meta-analysis

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              Blockade of B7-H1 improves myeloid dendritic cell-mediated antitumor immunity.

              Suppression of dendritic cell function in cancer patients is thought to contribute to the inhibition of immune responses and disease progression. Molecular mechanisms of this suppression remain elusive, however. Here, we show that a fraction of blood monocyte-derived myeloid dendritic cells (MDCs) express B7-H1, a member of the B7 family, on the cell surface. B7-H1 could be further upregulated by tumor environmental factors. Consistent with this finding, virtually all MDCs isolated from the tissues or draining lymph nodes of ovarian carcinomas express B7-H1. Blockade of B7-H1 enhanced MDC-mediated T-cell activation and was accompanied by downregulation of T-cell interleukin (IL)-10 and upregulation of IL-2 and interferon (IFN)-gamma. T cells conditioned with the B7-H1-blocked MDCs had a more potent ability to inhibit autologous human ovarian carcinoma growth in non-obese diabetic-severe combined immunodeficient (NOD-SCID) mice. Therefore, upregulation of B7-H1 on MDCs in the tumor microenvironment downregulates T-cell immunity. Blockade of B7-H1 represents one approach for cancer immunotherapy.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                07 July 2020
                July 2020
                : 12
                : 7
                : 1819
                Affiliations
                [1 ]Center for Gender-specific Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy; maria.bellenghi@ 123456iss.it (M.B.); rossella.puglisi@ 123456iss.it (R.P.); giada.pontecorvi@ 123456iss.it (G.P.); gianfranco.mattia@ 123456iss.it (G.M.)
                [2 ]Laboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy; alessandra.defeo@ 123456ior.it
                Author notes
                [* ]Correspondence: alessandra.care@ 123456iss.it ; Tel.: +39-0649902411
                [†]

                These authors contributed equally.

                Author information
                https://orcid.org/0000-0003-4106-3342
                Article
                cancers-12-01819
                10.3390/cancers12071819
                7408637
                32645881
                d14ab94f-7e0d-444a-8e5a-773e04993de5
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 04 June 2020
                : 03 July 2020
                Categories
                Review

                melanoma,sex/gender,sex-hormones,immunity,micrornas,immunotherapy

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