Treatment of increased lipid levels with sterol regulatory element binding protein cleavage-activating protein (SCAP) inhibitors

Patent metadata

Field	Value
Publication number	US-11331332-B2
Application number	US-202016823832-A
Country	US
Kind code	B2
Filing date	Mar 19, 2020
Priority date	Mar 20, 2019
Publication date	May 17, 2022
Grant date	May 17, 2022

Abstract

The present disclosure provides methods of treating subjects having increased lipid levels and/or increased triglyceride levels, methods of identifying subjects having an increased risk of developing an increased lipid level and/or increased triglyceride level, methods of detecting human Sterol Regulatory Element Binding Protein Cleavage-Activating Protein (SCAP) variant nucleic acid molecules and variant polypeptides, and SCAP variant nucleic acid molecules and variant polypeptides.

First claim

What is claimed is:

1. A method of treating a subject having increased total cholesterol, increased low density lipoprotein (LDL), increased serum lipid level, or increased triglycerides, the method comprising administering a SCAP inhibitor to the subject, wherein the SCAP inhibitor comprises an antisense nucleic acid molecule, a Cas protein and guide RNA (gRNA) that hybridizes to a gRNA recognition sequence within a SCAP genomic nucleic acid molecule, or a small molecule SCAP inhibitor.

2. The method according to claim 1 , further comprising detecting the presence or absence of a SCAP variant nucleic acid molecule encoding a human SCAP polypeptide in a biological sample from the subject, wherein the SCAP variant nucleic acid molecule is: i) a genomic nucleic acid molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:12 at positions corresponding to positions 61,695 to 62,267 according to SEQ ID NO:2, or the complement thereof, ii) an mRNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:14 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:4, or the complement thereof, or iii) a cDNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:16 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:6, or the complement thereof; and when the subject is SCAP reference, the subject is also administered a therapeutic agent that treats or inhibits an increased lipid level and/or an increased triglyceride level in a standard dosage amount, and when the subject is heterozygous for a SCAP variant nucleic acid molecule, the subject is also administered a therapeutic agent that treats or inhibits an increased lipid level and/or an increased triglyceride level in a dosage amount that is the same as or lower than the standard dosage amount.

3. A method of treating a subject with a therapeutic agent that treats or inhibits an increased lipid level and/or an increased triglyceride level, wherein the subject is suffering from an increased lipid level and/or an increased triglyceride level, the method comprising the steps of:
determining whether the subject has a SCAP variant nucleic acid molecule encoding a human SCAP polypeptide by:
obtaining or having obtained a biological sample from the subject; and
performing or having performed a genotyping assay on the biological sample to determine if the subject has a genotype comprising the SCAP variant nucleic acid molecule; and

when the subject is SCAP reference, then administering or continuing to administer to the subject the therapeutic agent that treats or inhibits the increased lipid level and/or an increased triglyceride level in a standard dosage amount, and administering to the subject a SCAP inhibitor; and
when the subject is heterozygous for the SCAP variant nucleic acid molecule, then administering or continuing to administer to the subject the therapeutic agent that treats or inhibits the increased lipid level and/or an increased triglyceride level in an amount that is the same as or lower than a standard dosage amount, and administering to the subject a SCAP inhibitor;
wherein the presence of a genotype having the SCAP variant nucleic acid molecule encoding the human SCAP polypeptide indicates the subject has a reduced risk of developing the increased lipid level and/or an increased triglyceride level;
wherein the SCAP variant nucleic acid molecule is: i) a genomic nucleic acid molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:12 at positions corresponding to positions 61,695 to 62,267 according to SEQ ID NO:2, or the complement thereof, ii) an mRNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:14 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:4, or the complement thereof, or iii) a cDNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:16 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:6, or the complement thereof; and
wherein the SCAP inhibitor comprises an antisense nucleic acid molecule, a small interfering RNA (siRNA), a short hairpin RNA (shRNA) that hybridizes to a SCAP mRNA, a Cas protein and guide RNA (gRNA) that hybridizes to a gRNA recognition sequence within a SCAP genomic nucleic acid molecule, or a small molecule SCAP inhibitor.

4. A method of identifying a human subject having an increased risk for developing an increased lipid level and/or increased triglyceride level, wherein the method comprises determining or having determined the presence or absence of a SCAP variant nucleic acid molecule encoding a human SCAP polypeptide in a biological sample obtained from the subject; wherein: when the human subject is SCAP reference, then the human subject has an increased risk for developing the increased lipid level and/or increased triglyceride level; and when the human subject is heterozygous for the SCAP variant nucleic acid molecule or homozygous for the SCAP variant nucleic acid molecule, then the human subject has a decreased risk for developing the increased lipid level and/or increased triglyceride level; wherein the SCAP variant nucleic acid molecule is: i) a genomic nucleic acid molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:12 at positions corresponding to positions 61,695 to 62,267 according to SEQ ID NO:2, or the complement thereof, ii) an mRNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:14 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:4, or the complement thereof, or iii) a cDNA molecule having a nucleotide sequence comprising the nucleotide sequence according to SEQ ID NO:16 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:6, or the complement thereof.

5. A method of detecting a human Sterol Regulatory Element Binding Protein Cleavage-Activating Protein (SCAP) variant nucleic acid molecule in a human subject comprising assaying a sample obtained from the human subject to determine whether a nucleic acid molecule in the sample comprises a nucleotide sequence comprising: i) the nucleotide sequence according to SEQ ID NO:12 at positions corresponding to positions 61,695 to 62,267 according to SEQ ID NO:2, or the complement thereof; ii) the nucleotide sequence according to SEQ ID NO:14 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:4, or the complement thereof or iii) the nucleotide sequence according to SEQ ID NO:16 at positions corresponding to positions 4,116 to 4,417 according to SEQ ID NO:6, or the complement thereof.

6. The method according to claim 5 , wherein the assay comprises sequencing at least a portion of the nucleic acid molecule, wherein the sequenced portion comprises: i) positions corresponding to positions 61,694 to 61,695 according to SEQ ID NO:2, or the complement thereof; ii) positions corresponding to positions 4,115 to 4,116 according to SEQ ID NO:4, or the complement thereof; or iii) positions corresponding to positions 4,115 to 4,116 according to SEQ ID NO:6, or the complement thereof.

7. The method according to claim 6 , wherein the assay comprises:
a) contacting the sample with a primer hybridizing to: i) a portion of the nucleotide sequence of SCAP genomic nucleic acid molecule that is proximate to positions corresponding to positions 61,694 to 61,695 according to SEQ ID NO:2; ii) a portion of the nucleotide sequence of SCAP mRNA molecule that is proximate to positions 4,115 to 4,116 according to SEQ ID NO:4; or iii) a portion of the nucleoti

Assignees

• Regeneron Pharma
• Univ Maryland

Inventors

• Gong Da-Wei
• Perry James A
• Shuldiner Alan
• Gosalia Nehal
• Van Hout Cristopher

Classifications

• C12Q2600/156

  Polymorphic or mutational markers · CPC title

• A61K31/7105 Primary

  Natural ribonucleic acids, i.e. containing only riboses attached to adenine, guanine, cytosine or uracil and having 3'-5' phosphodiester links · CPC title

• C12N2310/11

  Antisense · CPC title

• C12N9/22

  Ribonucleases {[RNase]; Deoxyribonucleases [DNase]} · CPC title

• C12N2320/34

  Allele or polymorphism specific uses · CPC title