IP Library › Granted Patent US 12,577,281
Granted Patent B2
US 12,577,281 · App. 17/921,577 · Granted Mar 17, 2026

Mitochondrial-derived peptides and analogs thereof for use as a therapy for age-related diseases including cancer

Inventors: Pinchas Cohen (Los Angeles, CA); Kelvin Yen (Los Angeles, CA); Su-Jeong Kim (Los Angeles, CA)
Assignee: University of Southern California
C07K14/47A61P29/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,577,281
App. No.
17/921,577
Granted
Mar 17, 2026
Kind
B2
Abstract

Described herein is a new mitochondrial peptide. This small peptide is capable of modulating cancer, through a variety of mechanisms including autophagy/apoptosis, reduction of tumor cell viability, inducing inflammatory response in senescent cells and conversion of macrophage cell type. Administration of the peptide, its analogs and derivatives thereof, are likely to be effective treatments for cancer therapy, including generation of synthetic analogs that further enhance or abrogate activity relative to the peptide.

Claims (6)

1 . A composition comprising:

a mitochondrial-derived peptide, wherein the mitochondrial-derived peptide comprises an amino acid sequence of any of SEQ ID NOs: 1-214, or wherein the mitochondrial-derived peptide comprises an amino acid sequence with at least 95% sequence identity to any of SEQ ID NOs: 1-215 but is different from SEQ ID NO:215.

2 . The composition of claim 1 , wherein the mitochondrial-derived peptide comprises an amino acid sequence of LLLAVGGSGGSLSLMLTLIRGLSK (SEQ ID NO: 72).

3 . The composition of claim 1 , wherein the mitochondrial-derived peptide is about 30-34 amino acids in length.

4 . The composition of claim 1 , wherein the mitochondrial-derived peptide possesses a post-translational or artificial modification, wherein the artificial modification comprises pegylation, fatty-acid conjugation, polypeptide extension, IgG-Fc, camptothecin (CPT), human serum albumin (HSA), elastin-like polypeptide (ELP), transferrin, or albumin modification.

5 . A pharmaceutical composition, comprising a mitochondrial-derived peptide of claim 1 and a pharmaceutically acceptable excipient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 26, 2022
From: COHEN, PINCHAS; YEN, KELVIN; KIM, SU-JEONG
To: UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 061550/0135 →
Continuity (2)
Provisional Application 63025495 · May 15, 2020
Related Publication 20230167161A1 · Jun 1, 2023
References Cited (15)
US 11124551B2 · Cohen et al. · 2021 [cited by applicant]
US 20170088852A1 · Dangoor et al. · 2017 [cited by applicant]
US 20180360910A1 · Cohen et al. · 2018 [cited by applicant]
WO 0181581A2 · 2001 [cited by applicant]
WO 2017223533A1 · 2017 [cited by applicant]
WO 2021231988A2 · 2021 [cited by applicant]
International Search Report and Written Opinion for PCT/US2021/032641, dated Nov. 26, 2021, 13 pages. [cited by applicant]
Kim et al., Mitochondrially derived peptides as novel regulators of metabolism, The Journal of Physiology, 2017, vol. 595(21), pp. 6613-6621. [cited by applicant]
Supplementary European Search Report for EP 21802909, dated Apr. 4, 2024, 8 pages. [cited by applicant]
Zuccato et al., Mitochondrial-derived peptide humanin as therapeutic target in cancer and degeneratie diseases, Expert Opinion on Therapeutic Targets, 2018, vol. 23(2), pp. 117-126. [cited by applicant]
Office Action for Application No. P6002399/2022 dated Mar. 12, 2025, 6 Pages. [cited by applicant]
Lee et al., The Mitochondrial-Derived Peptide MOTS-c Promotes Metabolic Homeostasis and Reduces Obesity and Insulin Resistance, Cell Metabolism, 2015, vol. 21, pp. 443-454. [cited by applicant]
Cobb et al., Naturally occurring mitochondrial-derived peptides are age-dependent regulators of apoptosis, insulin sensitivity, and inflammatory markers, Aging, 2016, vol. 8(4), pp. 796-809. [cited by applicant]
Yen et al., “Mitochondrial-derived microproteins: from discovery to function.” Trends in Genetics 41.2 (2025): 132-145. [cited by applicant]
European Examination Report from the European Patent Office for Application No. 21 802 909.9-1111, mailed Dec. 11, 2024 (5 pages). [cited by applicant]