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The epithelial-mesenchymal transition (EMT) shifts epithelial cells towards a malignant mesenchymal phenotype, enhancing their invasiveness and chemoresistance. Cancer cells initiate an “EMT program” for their metastatic dissemination and this in turn is governed by several transcription factors including Snail1, Slug (Snail2), Twist and Zeb that repress epithelial and activate mesenchymal transcriptional signatures [1]. Snail1 promotes tumor invasion, resistance to antineoplastic drugs, acquisition of cancer stem cell characteristics and metabolism reprogramming [1]. Besides, Snail1 controls activation of cancer-activated fibroblasts (CAFs) [2] (Figure 1). Accordingly, the expression of Snail1 is observed in the tumor-stroma interface of colorectal tumors [3] and in triple-negative breast cancer (TNBC), the most lethal and aggressive subtype [4]. Unfortunately, since Snail1 role was discovered in cancer cells, it has represented an elusive molecular target for therapeutic intervention. With this goal we have pointed to the Achilles’ heel of Snail1, which is its remarkable protein instability [5]. An extensive work has been done during the last years describing Snail1 lability in epithelial cells pushed by the action of several E3-ubiquitin ligases [6] (Figure 1). Cancer cells manage to counteract Snail1 protein degradation by activating signaling pathways, such us the Wnt/AKT/GSK3β, the Notch/β-catenin/AKT/GSK3β and others initiated by Hypoxia, DNA damage and cell stress [6]. Pathological Snail1 stabilization requires the specific down-regulation of one or several E3 ligases like FBXL14, the inactivation of kinases such us GSK3β required for β-TrCP1 degradation or the action of kinases enhancing Snail1 stability [6]. We have focused in an alternative scenario, on the enzymes that removed the ubiquitination mark, the deubiquitinases (DUBs). These DUBs are currently at the main focus of cancer research because are commonly deregulated in tumors [7]. To tackle the issue of DUBs action on Snail1 stability, we have performed an unbiased luminescent siRNA screening and identified USP27X as a bona fide DUB for Snail1. USP27X was validated by an extensive battery of biochemical assays testing the physical interaction with Snail1 and the capability to stabilize and to deubiquitinate Snail1 [5] (Figure 1). USP27X is detected in cancer cell lines and tumors with a 72 KDa molecular weight, higher than the expected because its translation occurs upstream of the canonical AUG codon [8]. This long form is enriched in the nucleus but also present in the cytosol. Although the existence of a protein translated from the canonical AUG has not been formally proven, a shorter form is detected in the cytosol of cancer cells, suggesting that different forms of USP27X might have specific roles. Functionally, USP27X is closely related to USP22 and to USP51, DUBs targeting monoubiquitinated H2B [8]. USP22 forms part of the SAGA complex and requires the participation of cofactors like ATXN7L3 and ENY2 to deubiquitinate H2B, while USP27X functions independently of SAGA but also needs ATXN7L3 and ENY2 to act on H2B [8]. The similar participation of cofactors has not been investigated for USP27X action on Snail1 or others substrates. When over-expressed, USP22 interacts with and stabilizes Snail1; however, the fact USP22 cannot compensate the lack of USP27X (in terms of Snail1 stability) suggest USP27X has a predominant role in Snail1 stabilization [5]. Therefore, several questions still need to be responded: 1) Might different forms of USP27X have a differential role in EMT? 2) Which is the relationship between USP27X and USP22? 3) Does USP27X require specific cofactors to deubiquitinate Snail1? The answer to these questions will Editorial

USP27X, a new player on EMT and fibroblast activation