IP Library Granted Patent US 12,667,565
Granted Patent B2
US 12,667,565 · App. 17/779,826 · Granted Jun 30, 2026

Use of composition for enhancing anticancer effect, comprising ERRy inhibitor as active ingredient

Inventors: Keun Gyu Park (Daegu, KR); In Kyu Lee (Daegu, KR); Sung Jin Cho (Daegu, KR); Yeon Kyung Choi (Daegu, KR); Mi Jin Kim (Daegu, KR); Jung Wook Chin (Daegu, KR); Yong Hyun Jeon (Daegu, KR); Jin A Kim (Daegu, KR); Dong Su Kim (Daegu, KR); Hoe Yune Jung (Pohang-si, KR)
Assignee: NOVMETAPHARMA CO., LTD.
A61K31/495A61K31/44A61K31/7105A61P35/00C07K16/2869C12N15/115G01N33/5758G01N33/6875
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Quick Facts
Patent No.
US 12,667,565
App. No.
17/779,826
Granted
Jun 30, 2026
Kind
B2
Abstract

The present invention relates to a pharmaceutical composition for inhibiting the resistance of liver cancer to sorafenib and enhancing an anticancer effect, comprising an Estrogen-related receptor γ (ERRγ) inhibitor as an active ingredient. The present invention can be effectively used as a pharmaceutical composition for treating sorafenib-resistant advanced liver cancer.

Claims (17)

1 . A method for diagnosis and treatment of sorafenib-resistant liver cancer, comprising the following steps:

(a) measuring an expression level of mRNA of an estrogen-related receptor γ (ERRγ) gene or a protein expressed therefrom in a biological sample isolated from a test patient with liver cancer;

(b) comparing the measured expression level of the ERRγ mRNA and/or the measured level of ERRγ protein of the test patient of step (a) with a reference expression level of ERRγ mRNA and/or a reference level of ERRγ protein, said reference expression level of ERRY mRNA and/or a reference level of ERRγ protein being obtained from a reference patient with a liver cancer other than sorafenib-resistant liver cancer,

wherein a higher measured expression level of the ERRγ mRNA than the reference expression level and/or a higher measured level of ERRγ protein than the reference level indicates that the test patient has sorafenib-resistant liver cancer; and

(c) administering to the test patent who is determined to have sorafenib-resistant liver cancer, (i) an agent capable of inhibiting ERRγ protein activity or ERRγ gene expression; (ii) a combination of sorafenib and an agent capable of inhibiting ERRγ protein activity or ERRγ gene expression.

2 . The method of claim 1 , wherein the biological sample comprises liver tissue, liver cells, whole blood, plasma, or serum.

3 . A method selected from the group consisting of:

(a) preventing or inhibiting a development of sorafenib resistance in a liver cancer patient who is prescribed for sorafenib treatment or underwent sorafenib treatment; and

(b) enhancing sorafenib treatment of a liver cancer patient,

said method comprising administering to the liver cancer patient an effective amount of an inverse agonist against estrogen-related receptor γ (ERRγ),

wherein the inverse agonist against ERRγ is a compound of the following Formula 1 or a pharmaceutically acceptable salt thereof:

4 . The method of claim 3 , which further comprises administering sorafenib, wherein the inverse agonist is administered simultaneously with sorafenib, separately, or sequentially.

5 . A method of treating liver cancer in a subject in need thereof, comprising:

administering an effective amount of an inverse agonist against estrogen-related receptor γ (ERRγ),

wherein the inverse agonist against ERRγ is a compound of the following Formula 1 or a pharmaceutically acceptable salt thereof:

6 . The method of claim 1 , wherein the agent is administered simultaneously with sorafenib, separately, or sequentially.

7 . The method of claim 5 , wherein the inverse agonist is administered simultaneously with sorafenib, separately, or sequentially.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2022
From: PARK, KEUN GYU; LEE, IN KYU; CHO, SUNG JIN; CHOI, YEON KYUNG; KIM, MI JIN; CHIN, JUNG WOOK; JEON, YONG HYUN; KIM, JIN A; KIM, DONG SU; JUNG, HOE YUNE
To: NOVMETAPHARMA CO., LTD.
Reel/Frame 060016/0131 →
Priority Claims (1)
KR 10-2019-0152827 · Nov 26, 2019 · national
Continuity (1)
Related Publication 20230017330A1 · Jan 19, 2023
References Cited (46)
US 6096874A · Wallace et al. · 2000 [cited by applicant]
US 10934303B2 · Hwang · 2021 [cited by examiner]
US 11285226B2 · Hwang et al. · 2022 [cited by applicant]
US 20050096384A1 · Forman et al. · 2005 [cited by applicant]
US 20190161490A1 · Hwang et al. · 2019 [cited by applicant]
US 20190167820A1 · Hwang et al. · 2019 [cited by applicant]
US 20210196655A1 · Kuo et al. · 2021 [cited by applicant]
CN 101836991A · 2010 [cited by applicant]
CN 105331584A · 2016 [cited by applicant]
CN 106255756A · 2016 [cited by applicant]
CN 106466306A · 2017 [cited by applicant]
CN 109055549A · 2018 [cited by applicant]
KR 1020120134939A · 2012 [cited by applicant]
KR 1020160043419A · 2016 [cited by applicant]
KR 1020170047827A · 2017 [cited by applicant]
KR 1020170079128A · 2017 [cited by applicant]
KR 1020190042370A · 2019 [cited by applicant]
KR 1020210065064A · 2021 [cited by applicant]
RU 2012148710A · 2014 [cited by applicant]
WO 2016111507A1 · 2016 [cited by applicant]
WO 2018174506A1 · 2018 [cited by applicant]
Kim, J.H. et al. Estrogen-related receptor γ is upregulated in liver cancer and its inhibition suppresses liver cancer cell proliferation via induction of p21 and p27. Exp Mol Med. Mar. 4, 2016;48(3):e213 (Year: 2016). [cited by examiner]
Méndez-Blanco et al. Sorafenib resistance in hepatocarcinoma: role of hypoxia-inducible factors. Experimental & Molecular Medicine (2018) 50:134 (Year: 2018). [cited by examiner]
Kim, J. et al. Exp Mol Med 48, e213 (2016). https://doi.org/10.1038/emm.2015.115 (Year: 2016). [cited by examiner]
Ji-Hyun Kim et al., “Estrogen-related receptor γ is upregulated in liver cancer and its inhibition suppresses liver cancer cell proliferation via induction of p21 and p27”, Experimental & Molecular Medicine, 2016, pp. 1… [cited by applicant]
Thoudam Debraj Singh et al., “A Novel Orally Active Inverse Agonist of Estrogen-related Receptor Gamma (ERRy), DN200434, A Booster of NIS in Anaplastic Thyroid Cancer”, Clinical Cancer Research, Apr. 22, 2019 (online pu… [cited by applicant]
Matthew G. Vander Heiden, “Targeting cancer metabolism: a therapeutic window opens”, Nature Reviews | Drug Discovery, Sep. 2011, pp. 671-684, vol. 10. [cited by applicant]
Josep M. Llovet, M.D. et al., “Sorafenib in Advanced Hepatocellular Carcinoma”, The New England Journal of Medicine, Jul. 24, 2008, pp. 378-390, vol. 395 No. 4. [cited by applicant]
Lorenzo Capussotti et al., “Major Liver Resections for Hepatocellular Carcinoma on Cirrhosis: Early and Long-Term Outcomes”, Liver Transplantation, Feb. 2004, pp. S64-68, vol. 10, No. 2, Supple 1. [cited by applicant]
H. Lang et al., “Liver resection for hepatocellular carcinoma in non-cirrhotic liver without underlying viral hepatitis”, British Journal of Surgery, 2005, pp. 198-202, vol. 92. [cited by applicant]
International Search Report for PCT/KR2020/016976, dated Mar. 15, 2021. [cited by applicant]
Notice of Allowance dated Jun. 30, 2025 in Chinese Application No. 202080082523.9. [cited by applicant]
Bo Yuan, et al., “MiR-940 inhibits hepatocellular carcinoma growth and correlates with prognosis of hepatocellular carcinoma patients”, Cancer Science, Jul. 2015, vol. 106, No. 7, pp. 819-824 (6 pages total). [cited by applicant]
T.T. Berezov, et al., “Biological Chemistry,” 1998, pp. 34 and 59 (4 pages total). [cited by applicant]
C.I. Pokrovsky, “Small Medical Encyclopedia,” 1991, vol. 1, p. 146 (4 pages total). [cited by applicant]
Guizhi Zhu, et al., “Aptamer-based targeted therapy,” Advanced Drug Delivery Reviews, 2018, pp. 1-14 (14 pages total), https://doi.org/10.1016/j.addr.2018.08.005. [cited by applicant]
O.P. Turkina, “Antisens Oligonucleotides,” APRIORI, Natural and Technical Sciences, 2017, No. 3, pp. 1-15 (15 pages total), https://elibrary.ru/download/elibrary_29329867_l 6900460.pdf. [cited by applicant]
Written Opinion issued Mar. 15, 2021 in Application No. PCT/KR2020/016976. [cited by applicant]
V.G. Belikov, Pharmaceutical Chemistry, 2007, pp. 27-29 (6 pages total). [cited by applicant]
D.A. Kharkevich, Pharmacology, 2010 (7 pages total). [cited by applicant]
V.N. Zhulenko et al., Pharmacology, 2008, pp. 34-35 (4 pages total). [cited by applicant]
Kazuomi Ueshima et al., “Molecular targeted agent for hepatocellular carcinoma,” Japanese Journal of Clinical Medicine, 2012, vol. 70, Suppl. 8, pp. 457-462 (8 pages total). [cited by applicant]
Jina Kim et al., “Discovery of Potent, Selective, and Orally Bioavailable Estrogen-Related Receptor-y Inverse Agonists to Restore the Sodium Iodide Symporter Function in Anaplastic Thyroid Cancer”, J. Med. Chem. Jan. 18… [cited by applicant]
Jens Hasskarl, “Sorafenib: targeting multiple tyrosine kinases in cancer”, Recent Results Cancer Res., 2014, vol. 201 (1 page total). [cited by applicant]
International Search Report issued Sep. 18, 2023 in Application No. PCT/IB2023/055661. [cited by applicant]
Written Opinion of the International Searching Authority issued Sep. 18, 2023 in Application No. PCT/IB2023/055661. [cited by applicant]