Treatment of increased lipid levels with sterol regulatory element binding transcription factor 1 (SREBF1) inhibitors

Patent metadata

Field	Value
Publication number	US-11504390-B2
Application number	US-202016823634-A
Country	US
Kind code	B2
Filing date	Mar 19, 2020
Priority date	Mar 20, 2019
Publication date	Nov 22, 2022
Grant date	Nov 22, 2022

Abstract

The present disclosure provides methods of treating subjects having increased lipid levels, methods of identifying subjects having an increased risk of developing an increased lipid level, methods of detecting human Sterol Regulatory Element Binding Transcription Factor 1 (SREBF1) variant nucleic acid molecules and variant polypeptides, and SREBF1 variant nucleic acid molecules and variant polypeptides.

First claim

What is claimed is:

1. A method of treating a subject having increased total cholesterol or increased low density lipoprotein (LDL), the method comprising administering an SREBF1 inhibitor to the subject, and further comprising detecting the presence or absence of an SREBF1 variant nucleic acid molecule encoding a human SREBF1 polypeptide in a biological sample from the subject, wherein the SREBF1 variant nucleic acid molecule comprises:
i) a genomic nucleic acid molecule having a nucleotide sequence comprising a thymine at a position corresponding to position 17,922 according to SEQ ID NO:2, or the complement thereof,
ii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,185 according to SEQ ID NO:6, or the complement thereof,
iii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,260 according to SEQ ID NO:7, or the complement thereof,
iv) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,056 according to SEQ ID NO:8, or the complement thereof,
v) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,185 according to SEQ ID NO:12, or the complement thereof,
vi) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,260 according to SEQ ID NO:13, or the complement thereof, and/or
vii) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,056 according to SEQ ID NO:14, or the complement thereof; and
when the subject is SREBF1 reference, the subject is also administered a therapeutic agent that treats or inhibits an increased lipid level in a standard dosage amount, and
when the subject is heterozygous for the SREBF1 variant nucleic acid molecule, the subject is also administered a therapeutic agent that treats or inhibits an increased lipid level in a dosage amount that is the same as or lower than the standard dosage amount; and
wherein the SREBF1 inhibitor comprises an antisense nucleic acid molecule that hybridizes to an SREBF1 mRNA, a small interfering RNA (siRNA) that hybridizes to an SREBF1 mRNA, a short hairpin RNA (shRNA) that hybridizes to an SREBF1 mRNA, Fatostatin A, or PF-429242.

2. A method of treating a subject with a therapeutic agent that treats or inhibits an increased lipid level, wherein the subject is suffering from an increased lipid level, the method comprising the steps of:
determining whether the subject has an SREBF1 variant nucleic acid molecule encoding a human SREBF1 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 SREBF1 variant nucleic acid molecule; and

when the subject is SREBF1 reference, then administering or continuing to administer to the subject the therapeutic agent that treats or inhibits the increased lipid level in a standard dosage amount, and administering to the subject an SREBF1 inhibitor; and
when the subject is heterozygous for the SREBF1 variant nucleic acid molecule, then administering or continuing to administer to the subject the therapeutic agent that treats or inhibits the increased lipid level in an amount that is the same as or lower than a standard dosage amount, and administering to the subject an SREBF1 inhibitor;
wherein the presence of a genotype having the SREBF1 variant nucleic acid molecule encoding the human SREBF1 polypeptide indicates the subject has a reduced risk of developing the increased lipid level;
wherein the increased lipid level is increased serum lipid level, increased total cholesterol, or increased LDL;
wherein the SREBF1 variant nucleic acid molecule comprises:
i) a genomic nucleic acid molecule having a nucleotide sequence comprising a thymine at a position corresponding to position 17,922 according to SEQ ID NO:2, or the complement thereof,
ii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,185 according to SEQ ID NO:6, or the complement thereof,
iii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,260 according to SEQ ID NO:7, or the complement thereof,
iv) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,056 according to SEQ ID NO:8, or the complement thereof,
v) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,185 according to SEQ ID NO:12, or the complement thereof,
vi) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,260 according to SEQ ID NO:13, or the complement thereof, and/or
vii) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,056 according to SEQ ID NO:14, or the complement thereof; and
wherein the SREBF1 inhibitor comprises an antisense nucleic acid molecule that hybridizes to an SREBF1 mRNA, a small interfering RNA (siRNA) that hybridizes to an SREBF1 mRNA, a short hairpin RNA (shRNA) that hybridizes to an SREBF1 mRNA, Fatostatin A, or PF-429242.

3. A method of identifying a human subject having an increased risk for developing an increased lipid level, wherein the method comprises determining or having determined the presence or absence of an SREBF1 variant nucleic acid molecule encoding a human SREBF1 polypeptide in a biological sample obtained from the subject; wherein: when the human subject is SREBF1 reference, then the human subject has an increased risk for developing the increased lipid level; and when the human subject is heterozygous for the SREBF1 variant nucleic acid molecule or homozygous for the SREBF1 variant nucleic acid molecule, then the human subject has a decreased risk for developing the increased lipid level; wherein the SREBF1 variant nucleic acid molecule comprises:
i) a genomic nucleic acid molecule having a nucleotide sequence comprising a thymine at a position corresponding to position 17,922 according to SEQ ID NO:2, or the complement thereof,
ii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,185 according to SEQ ID NO:6, or the complement thereof,
iii) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,260 according to SEQ ID NO:7, or the complement thereof,
iv) an mRNA molecule having a nucleotide sequence comprising a uracil at a position corresponding to position 1,056 according to SEQ ID NO:8, or the complement thereof,
v) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,185 according to SEQ ID NO:12, or the complement thereof,
vi) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine at a position corresponding to position 1,260 according to SEQ ID NO:13, or the complement thereof, and/or
vii) a cDNA molecule produced from an mRNA molecule in the sample, wherein the cDNA molecule has a nucleotide sequence comprising a thymine

Assignees

• Regeneron Pharma
• Univ Maryland

Inventors

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

Classifications

• C12Q1/6827

  for detection of mutation or polymorphism · CPC title

• C12Q1/6853

  using modified primers or templates · CPC title

• C12N2310/14

  interfering nucleic acids [NA] · CPC title

• C07K14/4702

  Regulators; Modulating activity · CPC title

• C12Q1/6883

  for diseases caused by alterations of genetic material · CPC title