Aberrant G protein signaling in nervous system tumors
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Stacey A Woods1, Eric Marmor, Matthias Feldkamp
1Arthur and Sonia Labatt Brain Tumor Research Centre, The Hospital for Sick Children, Toronto, Ontario, Canada.
Object:
Guanosine triphosphate (GTP)-binding proteins, also known as G proteins, play important roles in the regulation of cell growth and differentiation by transmitting intracellular signals from cell surface receptors. In this paper, the authors review G protein signaling in general and its aberrations in four human nervous system tumors.
Methods:
In the nervous system, four tumor types have been associated with aberrant G protein signaling. The first tumor type includes astrocytomas, which have increased levels of the activated form of the small G protein, p21-ras, without primary oncogenic p21-ras mutations. The likely source for increased p21-ras activity in sporadically occurring astrocytomas is overexpressed or constitutively activated growth factor receptors, whereas in neurofibromatosis Type 1 (NF1)-associated astrocytomas, the source is a loss of expression of neurofibromin, a major inactivator of p21-ras (ras-GTPase activating protein [GAP]). The second type of tumor associated with aberrant G protein signaling includes sporadic and NF1-associated neurofibromas and malignant peripheral nerve sheath tumors, which also have increased p21-ras activity due to a loss of neurofibromin expression. The third tumor type includes subependymal giant cell astrocytomas as part of the tuberous sclerosis complex (TSC). These tumors display a loss of tuberin expression due to germline mutations in the TSC2 gene. Tuberin functions as an inactivator of the small G protein rap1B (rap1-GAP) and, hence, loss of its expression could lead to increased rap1B activity. In addition to TSC-associated tumors, the authors demonstrate that the majority of sporadically occurring astrocytomas display either loss of tuberin or overexpression of rap1B. This suggests that increased rap1B activity, which can augment p21-ras-mediated signals, also contributes to G protein-mediated aberrant signaling in sporadically occurring astrocytomas. The fourth tumor type includes a significant subset of pituitary adenomas that show constitutive activation of the G alpha subunit of the large heterotrimeric G s protein, which is involved in hormone receptor signaling. The net result of this aberrant activation is increased cyclic adenosine monophosphate and mitogenic tumor-promoting signals.
Conclusions:
The authors' review of G protein signaling and aberrations in this process is made with the long-term view that increased understanding of relevant signaling pathways will eventually lead to novel biological targeted therapies against these tumors.
Insights
G protein signaling is crucial for cell regulation. Aberrations in G protein pathways are linked to nervous system tumors like astrocytomas, neurofibromas, and pituitary adenomas, offering targets for new therapies.
Area of Science:
- Molecular Biology
- Neuro-oncology
- Cell Signaling
Background:
- Guanosine triphosphate (GTP)-binding proteins (G proteins) regulate cell growth and differentiation via intracellular signal transduction.
- Aberrant G protein signaling is implicated in the development of various human nervous system tumors.
Purpose of the Study:
- To review the general mechanisms of G protein signaling.
- To examine the specific aberrations of G protein signaling in four types of human nervous system tumors.
Main Methods:
- Review of literature on G protein signaling pathways.
- Analysis of G protein pathway alterations in astrocytomas, neurofibromas, malignant peripheral nerve sheath tumors, and pituitary adenomas.
- Investigation of genetic mutations and protein expression levels associated with aberrant signaling.
Main Results:
- Astrocytomas show increased p21-ras activity due to growth factor receptor overexpression or loss of neurofibromin.
- Neurofibromas and malignant peripheral nerve sheath tumors exhibit elevated p21-ras activity from neurofibromin loss.
- Tuberous sclerosis complex-associated tumors involve loss of tuberin, potentially increasing rap1B activity.
- Sporadic astrocytomas and pituitary adenomas display dysregulated G protein signaling (e.g., rap1B, Gs alpha subunit) contributing to tumor growth.
Conclusions:
- Understanding G protein signaling aberrations is key to developing targeted therapies for nervous system tumors.
- Aberrant signaling in p21-ras, rap1B, and Gs proteins contributes to the pathogenesis of these tumors.
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