High Filamin a Expression in Adrenocortical Carcinomas Is Associated with a Favourable Tumour Behaviour: A European Multicentric Study Article Swipe
Rosa Catalano
,
Barbara Altieri
,
Anna Angelousi
,
Maura Arosio
,
Francesca Bravi
,
Letizia Canu
,
Giorgio Alberto Croci
,
Mario Detomas
,
Emanuela Esposito
,
Emanuele Ferrante
,
Stefano Ferrero
,
Carmina Teresa Fuß
,
Gregory Kaltsas
,
Otilia Kimpel
,
Laura‐Sophie Landwehr
,
Michaela Luconi
,
Valentina Morelli
,
Gabriella Nesi
,
Emma Nozza
,
Silviu Sbiera
,
A Șerban
,
Cristina L. Ronchi
,
Giovanna Mantovani
,
Erika Peverelli
·
YOU?
·
· 2023
· Open Access
·
· DOI: https://doi.org/10.3390/ijms242316573
YOU?
·
· 2023
· Open Access
·
· DOI: https://doi.org/10.3390/ijms242316573
The insulin-like growth factor 2 (IGF2) promotes cell growth by overactivating the IGF system in an autocrine loop in adrenocortical carcinomas (ACCs). The cytoskeleton protein filamin A (FLNA) acts as a repressor of IGF2 mitogenic signalling in ACC cells. The aims of this study were to test FLNA expression by immunohistochemistry in 119 ACCs and 26 adrenocortical adenomas (ACAs) and to evaluate its relationship with clinicopathological features and outcome in ACCs. We found that 71.4% of ACCs did not express FLNA, whereas FLNA absence was a rare event in ACAs (15.4%, p < 0.001 vs. ACCs). In addition, the expression of FLNA was associated with a less aggressive tumour behaviour in ACCs. Indeed, the subgroup of ACCs with high FLNA showed a lower ENSAT stage, Weiss score, and S-GRAS score compared to ACCs with low FLNA expression (p < 0.05). Moreover, patients with high FLNA had a longer overall survival than those with low FLNA (p < 0.05). In conclusion, our data suggest that FLNA may represent a “protective” factor in ACCs, and the integration of FLNA immunohistochemical expression in ACC tissues along with other clinical and molecular markers could be helpful to improve diagnostic accuracy and prognosis prediction in ACCs.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3390/ijms242316573
- https://www.mdpi.com/1422-0067/24/23/16573/pdf?version=1700567717
- OA Status
- gold
- Cited By
- 3
- References
- 53
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4388866410
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- OpenAlex ID
-
https://openalex.org/W4388866410Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.3390/ijms242316573Digital Object Identifier
- Title
-
High Filamin a Expression in Adrenocortical Carcinomas Is Associated with a Favourable Tumour Behaviour: A European Multicentric StudyWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2023Year of publication
- Publication date
-
2023-11-21Full publication date if available
- Authors
-
Rosa Catalano, Barbara Altieri, Anna Angelousi, Maura Arosio, Francesca Bravi, Letizia Canu, Giorgio Alberto Croci, Mario Detomas, Emanuela Esposito, Emanuele Ferrante, Stefano Ferrero, Carmina Teresa Fuß, Gregory Kaltsas, Otilia Kimpel, Laura‐Sophie Landwehr, Michaela Luconi, Valentina Morelli, Gabriella Nesi, Emma Nozza, Silviu Sbiera, A Șerban, Cristina L. Ronchi, Giovanna Mantovani, Erika PeverelliList of authors in order
- Landing page
-
https://doi.org/10.3390/ijms242316573Publisher landing page
- PDF URL
-
https://www.mdpi.com/1422-0067/24/23/16573/pdf?version=1700567717Direct link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
goldOpen access status per OpenAlex
- OA URL
-
https://www.mdpi.com/1422-0067/24/23/16573/pdf?version=1700567717Direct OA link when available
- Concepts
-
FLNA, Filamin, Autocrine signalling, Immunohistochemistry, Cancer research, Biology, Cancer, Internal medicine, Oncology, Medicine, Cell, Genetics, Receptor, CytoskeletonTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
3Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 2, 2024: 1Per-year citation counts (last 5 years)
- References (count)
-
53Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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