SSX addiction in melanoma propagates tumor growth and metastasis

Sofie Traynor, Malene Laage Ebstrup, Odd Lilleng Gammelgaard, Behzad Mansoori, Mikkel Green Terp, Cecilie Rose Hauge Rein, Sofie Rattenborg, Christina Bøg Pedersen, Henrik Jørn Ditzel, Morten Frier Gjerstorff*


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Cancer/testis antigens are receiving attention as targets for cancer therapy due to their germ- and cancer cell-restricted expression. However, many of these antigens are inconsistently expressed among cancer types and individual tumors. Here, we show that members of the SSX cancer/testis antigen family comprise attractive targets in the majority of melanoma patients, as SSX is expressed in more than 90% of primary melanomas and metastases and plays a critical role in metastatic progression. Accordingly, SSX silencing in melanoma mouse xenograft models reduced tumor growth and completely abolished the formation of metastatic lesions in lungs and livers. Mechanistically, we demonstrate that silencing SSX in melanoma cells induces cell cycle S-phase stalling, leading to proliferative arrest and enhanced apoptosis, which elucidates the inhibitory effect of SSX loss on tumor growth and colonization capacity. Silencing SSX further compromised the capacity of melanoma cells to migrate and invade, influencing these cells’ capability to spread and colonize. Taken together, these studies highlight SSX proteins as pivotal targets in melanoma with implications for blocking metastatic progression.

TidsskriftFrontiers in Oncology
Antal sider11
StatusUdgivet - 7. okt. 2022

Bibliografisk note

Funding Information:
This work was supported by Pink Tribute, Laege Sofus Carl Emil Friis og Hustru Olga Doris Friis Legat, Dagmar Marshalls Fond, the Danish Cancer Society, the Academy of Geriatric Cancer Research (AgeCare), the Novo Nordisk Foundation and the Danish Research Council for Independent Research.

Publisher Copyright:
Copyright © 2022 Traynor, Ebstrup, Gammelgaard, Mansoori, Terp, Rein, Rattenborg, Pedersen, Ditzel and Gjerstorff.


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