GIPC1 regulates MACC1-driven metastasis Article Swipe
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· 2023
· Open Access
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· DOI: https://doi.org/10.3389/fonc.2023.1280977
Background Identification of cancer metastasis-relevant molecular networks is desired to provide the basis for understanding and developing intervention strategies. Here we address the role of GIPC1 in the process of MACC1-driven metastasis. MACC1 is a prognostic indicator for patient metastasis formation and metastasis-free survival. MACC1 controls gene transcription, promotes motility, invasion and proliferation of colon cancer cells in vitro , and causes tumor growth and metastasis in mice. Methods By using yeast-two-hybrid assay, mass spectrometry, co-immunoprecipitation and peptide array we analyzed GIPC1 protein binding partners, by using the MACC1 gene promoter and chromatin immunoprecipitation and electrophoretic mobility shift assay we probed for GIPC1 as transcription factor. We employed GIPC1/MACC1-manipulated cell lines for in vitro and in vivo analyses, and we probed the GIPC1/MACC1 impact using human primary colorectal cancer (CRC) tissue. Results We identified MACC1 and its paralogue SH3BP4 as protein binding partners of the protein GIPC1, and we also demonstrated the binding of GIPC1 as transcription factor to the MACC1 promoter (TSS to -60 bp). GIPC1 knockdown reduced endogenous, but not CMV promoter-driven MACC1 expression, and diminished MACC1-induced cell migration and invasion. GIPC1 suppression reduced tumor growth and metastasis in mice intrasplenically transplanted with MACC1-overexpressing CRC cells. In human primary CRC specimens, GIPC1 correlates with MACC1 expression and is of prognostic value for metastasis formation and metastasis-free survival. Combination of MACC1 and GIPC1 expression improved patient survival prognosis, whereas SH3BP4 expression did not show any prognostic value. Conclusions We identified an important, dual function of GIPC1 - as protein interaction partner and as transcription factor of MACC1 – for tumor progression and cancer metastasis.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3389/fonc.2023.1280977
- https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1280977/pdf
- OA Status
- gold
- Cited By
- 1
- References
- 47
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4389479645
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W4389479645Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.3389/fonc.2023.1280977Digital Object Identifier
- Title
-
GIPC1 regulates MACC1-driven metastasisWork title
- Type
-
articleOpenAlex work type
- Language
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enPrimary language
- Publication year
-
2023Year of publication
- Publication date
-
2023-12-08Full publication date if available
- Authors
-
Franziska Siegel, Hannes Schmidt, Manisha Juneja, Janice Smith, Pia Herrmann, Dennis Kobelt, Kamal Sharma, Iduna Fichtner, Wolfgang Walther, Gunnar Dittmar, Rudolf Volkmer, Fritz G. Rathjen, Peter M. Schlag, Ulrike SteinList of authors in order
- Landing page
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https://doi.org/10.3389/fonc.2023.1280977Publisher landing page
- PDF URL
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https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1280977/pdfDirect link to full text PDF
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YesWhether a free full text is available
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goldOpen access status per OpenAlex
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https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1280977/pdfDirect OA link when available
- Concepts
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Metastasis, Gene knockdown, Chromatin immunoprecipitation, Cancer research, Transcription factor, Immunoprecipitation, Colorectal cancer, Biology, Electrophoretic mobility shift assay, Promoter, Chemistry, Gene, Gene expression, Cancer, GeneticsTop concepts (fields/topics) attached by OpenAlex
- Cited by
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1Total citation count in OpenAlex
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2025: 1Per-year citation counts (last 5 years)
- References (count)
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47Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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| referenced_works | https://openalex.org/W4315754639, https://openalex.org/W4322719806, https://openalex.org/W2114014236, https://openalex.org/W2907603303, https://openalex.org/W2095143857, https://openalex.org/W2670064607, https://openalex.org/W3032092952, https://openalex.org/W3017965839, https://openalex.org/W4281746488, https://openalex.org/W3125974259, https://openalex.org/W3135561803, https://openalex.org/W3214197925, https://openalex.org/W2003207814, https://openalex.org/W2234234909, https://openalex.org/W1966754581, https://openalex.org/W2125804654, https://openalex.org/W1998140525, https://openalex.org/W2124829726, https://openalex.org/W2009864060, https://openalex.org/W3114053654, https://openalex.org/W2081415074, https://openalex.org/W2088335631, https://openalex.org/W2003657314, https://openalex.org/W2164078562, https://openalex.org/W2078277807, https://openalex.org/W2084541361, https://openalex.org/W1985951459, https://openalex.org/W1970966441, https://openalex.org/W1967842430, https://openalex.org/W2109886015, https://openalex.org/W2119050497, https://openalex.org/W2048321210, https://openalex.org/W2109137601, https://openalex.org/W2103686156, https://openalex.org/W3177660183, https://openalex.org/W2110960566, https://openalex.org/W1564784444, https://openalex.org/W2114748778, https://openalex.org/W2095250075, https://openalex.org/W2180193980, https://openalex.org/W3026131022, https://openalex.org/W4210922095, https://openalex.org/W2204374538, https://openalex.org/W4281249676, https://openalex.org/W3042069114, https://openalex.org/W2620659693, https://openalex.org/W4213296330 |
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