Adams, DJ

Bishop, DT

Robles-Espinoza, CD

English

White Rose Research Online

Subscribe to PCMR and stay up-to-date with the only journal committed to publishing  basic research in melanoma and pigment cell biologyAs a member of the IFPCS or the SMR you automatically get online access to PCMR. Sign up as  a member today at www.ifpcs.org or at www.societymelanomaresarch.orgThe official journal ofINTERNATIONAL FEDERATION OF PIGMENT CELL SOCIETIES · SOCIETY FOR MELANOMA RESEARCHPIGMENT CELL & MELANOMAResearchTo take out a personal subscription, please click hereMore information about Pigment Cell & Melanoma Research at www.pigment.orgSubmit your next paper to PCMR online at http://mc.manuscriptcentral.com/pcmrDOI: 10.1111/pcmr.12833Volume 33, Issue 1, Pages 6–7Melanoma predisposition—A limited role for germline BRCA1 and BRCA2 variantsDavid J. Adams | David Timothy Bishop | Carla Daniela Robles-EspinozaIf you wish to order reprints of this article,  please see the guidelines hereEMAIL ALERTSReceive free email alerts and stay up-to-date on what is published  in Pigment Cell & Melanoma Research – click here6  |    Pigment Cell Melanoma Res. 2020;33:6–7.wileyonlinelibrary.com/journal/pcmr DOI: 10.1111/pcmr.12833  N E W S  A N D  V I E W SMelanoma predisposition—A limited role for germline BRCA1 and BRCA2 variantsDavid J. Adams  |   David Timothy Bishop |   Carla Daniela Robles‐EspinozaFor several decades, the role of germline BRCA1/BRCA2 variants in predisposition to melanoma has been controversial. Several groups have reported a positive association between BRCA variant status and melanoma formation, while other studies have failed to find an association (Gumaste et al., 2015). In the same way, analyses of fa‐milial melanoma cohorts have reported germline pathogenic alleles of BRCA2 (Gumaste et al., 2015; Tuominen et al., 2016) providing some evidence that germline variants in these genes might contrib‐ute to disease pathogenesis—but do they?The potential involvement of germline BRCA variants in melanoma susceptibility has profound implications for patient management and screening, since there are now agents such as poly‐(ADP‐ribose)‐polymerase (PARP) inhibitors (Farmer et al., 2005) that could be used to treat tumours from carrier patients, or even potentially prophy‐lactically to prevent tumour formation. Further, several commercial vendors promote BRCA1/2 testing in patients with a history of mel‐anoma, so it is important for patients and the healthcare system to establish whether such testing is warranted, not only because of the associated cost but also because genetic testing can be associated with significant patient anxiety.The tumour spectrum associated with germline BRCA variants has largely been elucidated by examining the cancer history of carri‐ers and presumed carriers in families identified because of multiple cases of breast or ovarian cancer. Of course, other cancers occur in these families both by chance but also potentially because the germ‐line variant increases cancer risk. Typically, the observed numbers of cancers in carriers are compared to the incidence of these cancers in the general population, but the power of individual studies is usually low because the number of actual carriers is limited. So why might the association between BRCA alleles and melanoma be inconsis‐tent? Firstly, it is possible that BRCA alleles have no effect and that chance variation provides a statistical signal suggesting an associa‐tion between these variants and melanoma. Secondly, that there is a modest effect and again chance variation plays a role. Thirdly, that any effect is limited to a subset of BRCA variants (e.g., the Ovarian Cancer Cluster Region which is associated with a much higher rela‐tive risk of ovarian cancer than other variants in BRCA1 or BRCA2 (Rebbeck et al., 2015)) and that the variant profile differs in differ‐ent cohorts. Finally, melanoma risk is not uniform across populations because common melanoma risk factors including pigmentation and nevi (which are unrelated to BRCA genotype) are polygenic. These variants, such as the R alleles of MC1R, are known to be able to in‐fluence the risk of melanoma development even in individuals with established high‐penetrance melanoma predisposition alleles such as pathogenic variants in CDKN2A. Identifying a suitable control population of a sufficient size, that is well‐matched to carriers and has the same melanoma polygenic risk profile, poses an additional problem and can confound the analysis.In a large‐scale and exhaustive study of cancers by the IMPACT team at Memorial Sloan Kettering Cancer Centre by Jonsson and collaborators, where cancer patients being treated at the hospi‐tal were uniformly ascertained and whose tumour and germline genomic sequences were systematically analysed by targeted se‐quencing, the authors were able to show that if germline BRCA1 or BRCA2 variants do contribute to the population burden of mel‐anoma predisposition then this contribution is modest. What is particularly special about this study is that the scale of the patient cohort (17,152 patients, 55 tumour types, 621 melanoma patients) meant that statistically robust conclusions could be derived. By analysis of these patients, clear and unequivocal associations be‐tween germline and somatic BRCA1/2 variants and ovarian, pros‐tate, breast and pancreas cancer (the BRCA‐associated cancer types) were observed, as well as a potentially novel association be‐tween somatic mutations in BRCA2 and uterine sarcomas. Indeed, it was only in the BRCA‐associated cancer types that genomic analysis was able to find a significant level of somatic loss‐of‐het‐erozygosity (LOH) consistent with the recessive model of tumour suppressor gene function. In comparison, when the same analysis was done on non‐BRCA‐associated cancer types (which includes melanoma), tumour‐specific loss of the germline pathogenic al‐lele instead of the wild‐type allele was observed more frequently, This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.© 2019 The Authors. Pigment Cell & Melanoma Research published by John Wiley & Sons LtdCoverage on: Jonsson, P., Bandlamudi, C., Cheng, M.L., Srinivasan, P., Chavan, S.S., Friedman, N.D., Rosen, E.Y., Richards, A.L., Bouvier, N., Selcuklu, S.D., Bielski, C.M., Abida, W., Mandelker, D., Birsoy, O., Zhang, L., Zehir, A., Donoghue, M.T.A., Baselga, J., Offit, K., Scher, H.I., O'Reilly, E.M., Stadler, Z.K., Schultz, N., Socci, N.D., Viale, A., Ladanyi, M., Robson, M.E., Hyman, D.M., Berger, M.F., Solit, D.B., Taylor, B.S. (2019). Tumour lineage shapes BRCA‐mediated phenotypes. Nature 571 (7766), 576–579.      |  7NEWS AND VIEWSfurther suggesting that loss of BRCA1 or BRCA2 did not contrib‐ute to these cancers. Moreover, it was only in ovarian, prostate, breast and pancreas cancer that the diagnostic single nucleotide pattern associated with loss of homologous recombination could be observed, with only a modest increase of this signature in non‐BRCA‐associated cancer types with biallelic BRCA inactivation. For the other cancer sites, only between 0.5% and a few per cent of cases had a germline BRCA variant (1% for melanoma). These figures are broadly in keeping with the make‐up of the popula‐tion studied of whom more than 18% were of Ashkenazi descent, a population known to have a high carrier rate of BRCA variants. As for the 621 melanoma patients in the study, there were 258 females and 363 males, and the mean and median age at first diag‐nosis were 56.9 and 59 years old, respectively, with age unknown for 26 patients.Another key observation of this study was that while patients from BRCA‐associated cancer types that had a germline, poten‐tially pathogenic BRCA variant derived greater clinical benefit from PARP inhibitor treatment than those without these variants, this was not true for patients with non‐BRCA‐associated cancers. Although their analysis only included one melanoma patient, it suggests that germline testing should not be the only criterium by which patient treatment is chosen and that other aspects such as tumour lineage might play an equal, if not more important, role in therapy response.Are there any limitations of the current study? In the context of melanoma, the authors grouped together all melanoma subtypes in‐cluding cutaneous, uveal, acral and mucosal melanoma. It is known that the genomes of these different melanoma subtypes are dis‐tinctly different, with the genomes of uveal, acral and mucosal mel‐anoma being characterized by a high level of copy number gains and losses, while the genomes of cutaneous melanoma are replete with UV‐induced C > T mutations. By “pooling” all subtypes together in this way it is possible that any statistical signal that might link BRCA1 or BRCA2 variants to rarer melanoma subtypes could be diluted. That said, on balance, it seems unlikely that germline BRCA1 or BRCA2 variants profoundly contribute to any melanoma subtype. It should be noted that large‐scale studies of this type cannot conclude that BRCA1 or BRCA2 variants never contribute to melanoma formation, just that at a population level they are not major contributors to the burden of disease.In summary, Jonsson et al. have made a significant contribution to the debate on the involvement of BRCA1 and BRCA2 variants to melanoma predisposition and provide a reminder that we must con‐stantly revisit gene‐disease associations so as to better counsel pa‐tients about their care.ORCIDDavid J. Adams  https://orcid.org/0000‐0001‐9490‐0306 Carla Daniela Robles‐Espinoza  https://orcid.org/0000‐0003‐3277‐7466 R E FE R E N C E SFarmer, H., McCabe, N., Lord, C. J., Tutt, A. N. J., Johnson, D. A., Richardson, T. B., … Ashworth, A. (2005). Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature, 434, 917–921. https ://doi.org/10.1038/natur e03445Gumaste, P. V., Penn, L. A., Cymerman, R. M., Kirchhoff, T., Polsky, D., & Mclellan, B. (2015). Skin cancer risk in BRCA1/2 mutation carriers. British Journal of Dermatology, 172, 1498–1506.Rebbeck, T. R., Mitra, N., Wan, F., Sinilnikova, O. M., Healey, S., Mcguffog, L., … Andrulis, I. (2015). Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer. JAMA, 313, 1347–1361.Tuominen, R., Engstrom, P. G., Helgadottir, H., Eriksson, H., Unneberg, P., Kjellqvist, S., … Höiom, V. (2016). The role of germline alterations in the DNA damage response genes BRIP1 and BRCA2 in melanoma susceptibility. Genes, Chromosomes & Cancer, 55, 601–611.

Melanoma predisposition—A limited role for germline BRCA1 and BRCA2 variants

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Melanoma predisposition—A limited role for germline BRCA1 and BRCA2 variants

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