FSCN1 as a new druggable target in adrenocortical carcinoma

• Published in: International journal of cancer Vol. 153; no. 1; pp. 210 - 223
• Main Authors: Ruggiero, Carmen, Tamburello, Mariangela, Rossini, Elisa, Zini, Silvia, Durand, Nelly, Cantini, Giulia, Cioppi, Francesca, Hantel, Constanze, Kiseljak‐Vassiliades, Katja, Wierman, Margaret E., Landwehr, Laura‐Sophie, Weigand, Isabel, Kurlbaum, Max, Zizioli, Daniela, Turtoi, Andrei, Yang, Shengyu, Berruti, Alfredo, Luconi, Michaela, Sigala, Sandra, Lalli, Enzo
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.07.2023; Wiley Subscription Services, Inc; Wiley
• Subjects: Actin; Adrenal Cortex Neoplasms - drug therapy; Adrenal Cortex Neoplasms - genetics; Adrenal Cortex Neoplasms - metabolism; adrenocortical carcinoma; Adrenocortical Carcinoma - drug therapy; Adrenocortical Carcinoma - genetics; Adrenocortical Carcinoma - metabolism; Animals; Cancer; Cell adhesion; Cell Line, Tumor; Cell Proliferation; Clinical trials; CRISPR; Cytoskeleton; Danio rerio; endocrine cancer; Filopodia; Gene Expression Regulation, Neoplastic; Guanine nucleotide exchange factor; Invasiveness; Lamellipodia; Life Sciences; Malignancy; Medical research; Metastases; Metastasis; Neoplasm Recurrence, Local - drug therapy; Neoplasm Recurrence, Local - genetics; Neuroendocrine tumors; Synergism; Zebrafish; cytoskeleton; adrenocortical carcinoma; endocrine cancer; Cytoskeleton; Adrenocortical carcinoma; Endocrine cancer
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/ijc.34526

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with a high risk of relapse and metastatic spread. The actin‐bundling protein fascin (FSCN1) is overexpressed in aggressive ACC and represents a reliable prognostic indicator. FSCN1 has been shown to synergize with VAV2, a guanine nucleotide exchange factor for the Rho/Rac GTPase family, to enhance the invasion properties of ACC cancer cells. Based on those results, we investigated the effects of FSCN1 inactivation by CRISPR/Cas9 or pharmacological blockade on the invasive properties of ACC cells, both in vitro and in an in vivo metastatic ACC zebrafish model. Here, we showed that FSCN1 is a transcriptional target for β‐catenin in H295R ACC cells and that its inactivation resulted in defects in cell attachment and proliferation. FSCN1 knock‐out modulated the expression of genes involved in cytoskeleton dynamics and cell adhesion. When Steroidogenic Factor‐1 (SF‐1) dosage was upregulated in H295R cells, activating their invasive capacities, FSCN1 knock‐out reduced the number of filopodia, lamellipodia/ruffles and focal adhesions, while decreasing cell invasion in Matrigel. Similar effects were produced by the FSCN1 inhibitor G2‐044, which also diminished the invasion of other ACC cell lines expressing lower levels of FSCN1 than H295R. In the zebrafish model, metastases formation was significantly reduced in FSCN1 knock‐out cells and G2‐044 significantly reduced the number of metastases formed by ACC cells. Our results indicate that FSCN1 is a new druggable target for ACC and provide the rationale for future clinical trials with FSCN1 inhibitors in patients with ACC. What's new? Adrenocortical carcinoma (ACC), though rare, has a high risk of relapse and metastasis. Aggressive ACC overexpresses the actin‐bundling protein fascin (FSCN1), and it is used as a prognostic indicator. Here, the authors investigated the effect of inactivating FSCN1 as a possible means of targeting the cancer. They found that FSCN1 inactivation reduced the invasiveness of ACC cells in vitro and in a zebrafish model, reduced the ability of ACC to proliferate. These results suggest FSCN1 could be a useful druggable target for controlling ACC.