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Amyloid Proteins From Medullary Thyroid Cancer and Laryngeal Amyloidosis

An ex Vivo Study to Purify Amyloid Fibrils and Solve Their 3D Structures Using Amyloid Proteins From Medullary Thyroid Cancer and Laryngeal Amyloidosis

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04760171
Enrollment
10
Registered
2021-02-18
Start date
2021-02-28
Completion date
2026-02-28
Last updated
2021-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease, Amyloid, Dementia, Medullary Thyroid Cancer

Brief summary

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.

Detailed description

This is an anonymous, voluntary inclusion, laboratory based, basic science research study. Appropriate patients who meet the inclusion criteria and complete the consent process will be asked to donate a small sample of excess tumour tissue after the completion of their surgical procedure. This tissue will be transferred to the research laboratory in Leeds University for analysis and subject to a variety of investigations and scientific procedures to achieve the study objectives. These include: 1. \- amyloid extraction by tissue homogenization and centrifugation as already documented in the literature. 2. \- mass spectrometry analysis to identify and characterize the most prominent proteins present in the amyloid deposits and their possible post-translational modifications. 3. \- Transmission Electron Microscopy to characterize at 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). 4. \- Atomic Force microscopy to characterize helical parameters of the amyloid fibrils needed to calculate the structure from Cryo-EM data. 5. \- Cryo-Electron Microscopy to elucidate the structure of the amyloids extracted from tissue affected in each disease

Interventions

None listed

Sponsors

University of Leeds
CollaboratorOTHER
The Leeds Teaching Hospitals NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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.

Design outcomes

Primary

MeasureTime frameDescription
Amyloid extraction by tissue homogenization and centrifugation12-24 monthsA standard laboratory technique for subsequent analysis
Transmission electron microscopy12-24 monthsTo 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).
Atomic force microscopy12-24 monthsTo characterize helical parameters of the amyloid fibrils needed to calculate the structure from Cryo-EM data.
Cryo-electron microscopy (Cryo-EM)12-24 monthsTo elucidate the structure of the amyloids extracted from tissue affected in each disease
Mass spectrometry12-24 monthsAnalysis to identify and characterize the most prominent proteins present in the amyloid deposits and their possible post-translational modifications.

Contacts

Primary ContactAnne Gowing
anne.gowing@nhs.net+441132060469

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026