Alzheimer Disease Clinical Trial
Official title:
An ex Vivo Study to Purify Amyloid Fibrils and Solve Their 3D Structures Using Amyloid Proteins From Medullary Thyroid Cancer and Laryngeal Amyloidosis
Using excess tumour samples that contain amyoid, from patients with Medullary Thyroid Cancer, we aim to determine the structures of ex vivo amyloid fibrils from human tumour tissue samples and compare them with that of existing stock of in vitro formed amyloid fibrils. This will permit the analysis of the effects of gene mutation and post-translational modification on the development of amyloid from a disease state. Amyloid is known to accumulate in the brain tissue of patients with neuro-degenerative conditions such as Alzheimer's disease and Dementia. Therefore solving the structure of amyloid fibrils may aid the development of future treatments for these conditions.
Status | Not yet recruiting |
Enrollment | 10 |
Est. completion date | February 2026 |
Est. primary completion date | February 2023 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Diagnosed with known or suspected MTC or LA - Age >= 18 years, no upper age limit - Able to provide informed consent for both surgical treatment and inclusion into this study - For MTC patients, treatment recommendation from the Thyroid MDT is for either hemithyroidectomy or total thyroidectomy - for LA patients, agreement with their attending clinician to undergo surgical debulking of disease under general anaesthetic. The procedure is called 'microlaryngoscopy and biopsy/debulking' Exclusion Criteria: - No known or suspected diagnosis of MTC or LA - Age <18 years - Unable to provide informed consent - Treatment recommendation from Thyroid MDT is for any treatment excluding primary surgery (ie palliation, best supportive care, chemotherapy, radiotherapy etc) - For LA patients, no agreement between patient and attending clinician to proceed with surgery as primary treatment. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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The Leeds Teaching Hospitals NHS Trust | University of Leeds |
Gallardo R, Iadanza MG, Xu Y, Heath GR, Foster R, Radford SE, Ranson NA. Fibril structures of diabetes-related amylin variants reveal a basis for surface-templated assembly. Nat Struct Mol Biol. 2020 Nov;27(11):1048-1056. doi: 10.1038/s41594-020-0496-3. Epub 2020 Sep 14. Erratum in: Nat Struct Mol Biol. 2020 Oct 9;:. — View Citation
Gallardo R, Ranson NA, Radford SE. Amyloid structures: much more than just a cross-ß fold. Curr Opin Struct Biol. 2020 Feb;60:7-16. doi: 10.1016/j.sbi.2019.09.001. Epub 2019 Nov 1. Review. — View Citation
GBD 2016 Neurology Collaborators. Global, regional, and national burden of neurological disorders, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2019 May;18(5):459-480. doi: 10.1016/S1474-4422(18)30499-X. Epub 2019 Mar 14. — View Citation
Knowles TP, Vendruscolo M, Dobson CM. The amyloid state and its association with protein misfolding diseases. Nat Rev Mol Cell Biol. 2014 Jun;15(6):384-96. doi: 10.1038/nrm3810. Review. Erratum in: Nat Rev Mol Cell Biol. 2014 Jul;15(7):496. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Amyloid extraction by tissue homogenization and centrifugation | A standard laboratory technique for subsequent analysis | 12-24 months | |
Primary | Transmission electron microscopy | To characterize the gross features of the extracted amyloid fibrils at low resolution (>20Å). This relatively simple procedure allows for quick characterization of the samples in order to optimize them for Atomic Force Microscopy (AFM) and Cryo-Electron Microscopy (Cryo-EM). | 12-24 months | |
Primary | Atomic force microscopy | To characterize helical parameters of the amyloid fibrils needed to calculate the structure from Cryo-EM data. | 12-24 months | |
Primary | Cryo-electron microscopy (Cryo-EM) | To elucidate the structure of the amyloids extracted from tissue affected in each disease | 12-24 months | |
Primary | Mass spectrometry | Analysis to identify and characterize the most prominent proteins present in the amyloid deposits and their possible post-translational modifications. | 12-24 months |
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