Methods and compositions for diagnosis and management of neurodegerative diseases

US11214835B1 · US · B1

Patent metadata
FieldValue
Publication numberUS-11214835-B1
Application numberUS-201816001880-A
CountryUS
Kind codeB1
Filing dateJun 6, 2018
Priority dateJun 6, 2017
Publication dateJan 4, 2022
Grant dateJan 4, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Described herein are assays, methods, and devices for diagnosing/prognosing Alzheimer's disease (AD) and/or a neurodegenerative disease in a subject. The assays, methods, and/or devices described herein can be configured to detect GAS5 long-coding RNAs and/or expression thereof in a sample from a subject.

First claim

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We claim: 1. A method of treating Alzheimer's disease, diabetes, or diabetes and Alzheimer's disease in a subject in need thereof, the method comprising: administering a therapeutically effective amount of a compound having a structure of formula 1 wherein R 1 is a methyl, an isobutane, a phenyl, an indole, or a butanamine, wherein R 2 is an ethylbenzene, an ethylcyclohexane, an isopentane, a phenyl, a propanamine, or a methylcyclopropane, wherein R 3 is a methylcyclopropane, a propionic acid, an ethylbenzene, or a propanamine wherein R 4 is a butanamine, a propionic acid, or a phenyl, wherein R 5 is a methylcyclopropane, a propionic acid, or an ethylbenzene, wherein R 6 is a phenyl, a propionic acid, an isobutene, and wherein R 7 is a phenyl, a propionic acid, a butanamine, or a methyl; or a pharmaceutical formulation thereof, to the subject in need thereof. 2. The method of claim 1 , wherein the compound has a structure according to any one of Formulas 3-4, 6-19, 3. The method of claim 2 , wherein the compound is capable of binding a GAS5 long non-coding RNA. 4. The method of claim 3 , wherein the GAS5 long non-coding RNA has a sequence that is 90%-100% identical to SEQ ID NO: 1. 5. The method of claim 2 , wherein administering occurs via oral, rectal, intraocular, inhaled, intranasal, topical, vaginal, parenteral, subcutaneous, intramuscular, intravenous, or intradermal administration. 6. The method of claim 1 , wherein the compound is capable of binding a GAS5 long non-coding RNA. 7. The method of claim 6 , wherein the GAS5 long non-coding RNA has a sequence that is 90%-100% identical to SEQ ID NO: 1. 8. The method of claim 1 , wherein a pharmaceutical formulation is administered to the subject in need thereof and the pharmaceutical formulation further comprises an agent selected from the group consisting of: antisense or RNA interference molecules, chemotherapeutics, antineoplastic agents, hormones, antibiotics, antivirals, immunomodulating agents, antinausea, pain modifying agents, anti-inflammatory agents, antipyretics, antibiotics, antibodies, antibody fragments, and any combination thereof. 9. The method of claim 1 , further comprising contacting a sample from the subject in need thereof or component thereof with a capture molecule, wherein the capture molecule is configured to specifically bind to a biomarker, wherein the biomarker is gas5 (SNHG2); and detecting specific binding of the biomarker to the capture molecule. 10. The method of claim 9 , wherein the step of detecting specific binding of the biomarker to the capture molecule is performed using a method comprising a technique selected from the group consisting of: array polymerase chain reaction (PCR), quantitative PCR (qPCR), real-time PCR, real-time qPCR, reverse-transcription PCR (RT-PCR), real-time RT-PCR, RT-qPCR, real-time RT-qPCR, digital PCR (dPCR), RNA flare, (LATE)-PCR, RNA flow cytometry, nucleotide sequencing, cell-based RNA detection assays, in situ hybridization, northern blot analysis, and any combination thereof. 11. The method of claim 9 , wherein the capture molecule has a sequence that is 95%-100% identical to any one of SEQ ID NOs.: 2-3. 12. The method of claim 1 , wherein the subject is greater than 45 years of age. 13. The method of claim 1 , wherein the subject is less than 45 years of age. 14. The method of claim 1 , wherein the subject has or is suspected of having diabetes.

Assignees

Inventors

Classifications

  • miRNA, siRNA or ncRNA · CPC title

  • C12Q1/6883Primary

    for diseases caused by alterations of genetic material · CPC title

  • Heterocyclic compounds · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

  • A61K31/404Primary

    Indoles, e.g. pindolol · CPC title

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Frequently asked questions

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What does patent US11214835B1 cover?
Described herein are assays, methods, and devices for diagnosing/prognosing Alzheimer's disease (AD) and/or a neurodegenerative disease in a subject. The assays, methods, and/or devices described herein can be configured to detect GAS5 long-coding RNAs and/or expression thereof in a sample from a subject.
Who is the assignee on this patent?
Patel Niketa A, Cai Jianfeng, Univ South Florida
What technology area does this patent fall under?
Primary CPC classification C12Q1/6883. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).