Ankrd1 Promotes Lamellipodia Formation and Cell Motility via Interaction with Talin-1 in Clear Cell Renal Cell Carcinoma
Ankyrin repeat domain 1 (Ankrd1), a transcriptional target of Yes-associated protein (YAP), is linked to cardiomyopathy. However, its role in cancer, particularly in clear cell renal cell carcinoma (ccRCC), remains vague. In this study, we examined the expression, regulation, and function of Ankrd1 in ccRCC. High Ankrd1 expression was related to poor prognosis in patients with ccRCC in The Cancer Genome Atlas cohort. Ankrd1 expression was regulated by YAP in all ccRCC cell lines examined and also by ERK5 in a subset of ccRCC cell lines. Moreover, silencing of Ankrd1 in ccRCC cell lines resulted in decreased cell motility, whereas its overexpression increased the cell motility. Ankrd1 colocalized with F-actin in lamellipodia upon phorbol ester stimulation. Ankrd1 silencing resulted in alterations in the shape of RCC cells and caused a decrease in lamellipodia formation. Ankrd1 also colocalized with talin-1 in lamellipodia. Ankrd1 depletion repressed talin-1-mediated activation of the integrin pathway. Immunohistochemical examination of surgical specimens revealed high expression of Ankrd1 in metastatic RCC tissues compared with that in primary RCC tissues from the same patients. Collectively, these findings suggest that Ankrd1 plays a critical role in the motility of ccRCC cells through lamellipodia formation.
Authors
- Takafumi Narisawa (ORCID: https://orcid.org/0000-0003-4062-2675)
- Sei Naito (ORCID: https://orcid.org/0000-0002-6104-4344)
- Norihiko Tsuchiya (ORCID: https://orcid.org/0000-0003-4242-2618)
- Mayu Yagi
- Osamu Ichiyanagi (ORCID: https://orcid.org/0000-0003-4573-5003)
- Masaki Ushijima
- Shigemitsu Horie
- Hideo Ito (ORCID: https://orcid.org/0000-0001-9605-8570)
- Y. TAKAI
Institutions
- Yamagata University (JP)
Publication Details
- Journal
- International Journal of Molecular Sciences
- Published
- 2025-04-29
- DOI
- https://doi.org/10.3390/ijms26094232
- Primary Topic
- Hippo pathway signaling and YAP/TAZ
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Society for the Promotion of Science