SERPINA12 promotes the tumorigenic capacity of HCC stem cells through hyperactivation of AKT/beta-catenin signaling

Background and Aims: HCC is an aggressive disease with poor clinical outcome. Understanding the mechanisms that drive cancer stemness, which we now know is the root cause of therapy failure and tumor recurrence, is fundamental for designing improved therapeutic strategies. This study aims to identify molecular players specific to CD133(+) HCC to better design drugs that can precisely interfere with cancer stem cells but not normal stem cell function. Approach and Results: Transcriptome profiling comparison of epithelial-specific normal CD133(+) cells isolated from fetal and regenerating liver against HCC CD133(+) cells isolated from proto-oncogene-driven and inflammation-associated HCC revealed preferential overexpression of SERPINA12 in HCC but not fetal and regenerating liver CD133(+) cells. SERPINA12 upregulation in HCC is tightly associated with aggressive clinical and stemness features, including survival, tumor stage, cirrhosis, and stemness signatures. Enrichment of SERPINA12 in HCC is mediated by promoter binding of the well-recognized beta-catenin effector TCF7L2 to drive SERPINA12 transcriptional activity. Functional characterization identified a unique and novel role of endogenous SERPINA12 in promoting self-renewal, therapy resistance, and metastatic abilities. Mechanistically, SERPINA12 functioned through binding to GRP78, resulting in a hyperactivated AKT/GSK3 beta/beta-catenin signaling cascade, forming a positive feed-forward loop. Intravenous administration of rAAV8-shSERPINA12 sensitized HCC cells to sorafenib and impeded the cancer stem cell subset in an immunocompetent HCC mouse model. Conclusions: Collectively, our findings revealed that SERPINA12 is preferentially overexpressed in epithelial HCC CD133+ cells and is a key contributor to HCC initiation and progression by driving an AKT/beta-catenin feed-forward loop.

Automated summary

This study aims to identify molecular factors specific to CD133(+) HCC and discover their role in cancer stemness. Transcriptome profiling revealed the overexpression of SERPINA12 in HCC CD133(+) cells, which is associated with aggressive clinical features and stemness signatures. Functional characterization showed that SERPINA12 promotes self-renewal, therapy resistance, and metastasis by activating the AKT/beta-catenin signaling cascade through binding to GRP78.