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WO2012087004A3 - Use of upr signaling pathway genes ire1 and hxl1 for treatment of fungal infection and meningitis - Google Patents

Use of upr signaling pathway genes ire1 and hxl1 for treatment of fungal infection and meningitis Download PDF

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Publication number
WO2012087004A3
WO2012087004A3 PCT/KR2011/009862 KR2011009862W WO2012087004A3 WO 2012087004 A3 WO2012087004 A3 WO 2012087004A3 KR 2011009862 W KR2011009862 W KR 2011009862W WO 2012087004 A3 WO2012087004 A3 WO 2012087004A3
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WIPO (PCT)
Prior art keywords
meningitis
hxl1
ire1
treatment
effect
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/KR2011/009862
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French (fr)
Other versions
WO2012087004A2 (en
Inventor
Yong Sun Bahn
Kwang Woo Jung
Hyun Ah Kang
Seon Ah Cheon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Industry Academic Cooperation Foundation of Chung Ang University
Industry Academic Cooperation Foundation of Yonsei University
Original Assignee
Industry Academic Cooperation Foundation of Chung Ang University
Industry Academic Cooperation Foundation of Yonsei University
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Application filed by Industry Academic Cooperation Foundation of Chung Ang University, Industry Academic Cooperation Foundation of Yonsei University filed Critical Industry Academic Cooperation Foundation of Chung Ang University
Publication of WO2012087004A2 publication Critical patent/WO2012087004A2/en
Publication of WO2012087004A3 publication Critical patent/WO2012087004A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • G01N33/502Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
    • G01N33/5041Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects involving analysis of members of signalling pathways
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Abstract

The present invention relates to the use of the UPR signaling pathway genes IRE1 and HXL1 for treatment of fungal infection and meningitis. In the invention, it was newly found that disruption of Ire1 and Hxl1 (HAC1 and XBP1-Like gene 1) proteins, newly identified in Cryptococcus neoformans, genes encoding the proteins, provides an antifungal effect and a meningitis-treating effect. Based on this finding, a candidate which can show a synergistic effect when being co-administered with an existing antifungal agent or meningitis-treating agent can be screened and a novel pharmaceutical composition having an antifungal effect and a meningitis-treating effect can be provided.
PCT/KR2011/009862 2010-12-23 2011-12-20 Use of upr signaling pathway genes ire1 and hxl1 for treatment of fungal infection and meningitis Ceased WO2012087004A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020100133885A KR101311196B1 (en) 2010-12-23 2010-12-23 Use of IRE1 gene and HXL1 gene in UPR signal pathway for treating mycoses or meningoencephalitis
KR10-2010-0133885 2010-12-23

Publications (2)

Publication Number Publication Date
WO2012087004A2 WO2012087004A2 (en) 2012-06-28
WO2012087004A3 true WO2012087004A3 (en) 2012-10-04

Family

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Application Number Title Priority Date Filing Date
PCT/KR2011/009862 Ceased WO2012087004A2 (en) 2010-12-23 2011-12-20 Use of upr signaling pathway genes ire1 and hxl1 for treatment of fungal infection and meningitis

Country Status (2)

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KR (1) KR101311196B1 (en)
WO (1) WO2012087004A2 (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104164443B (en) * 2014-07-14 2016-11-16 东华大学 A dual-luciferase monitoring plasmid for detecting UPR levels in living yeast cells and its construction and application
RS62386B1 (en) * 2014-10-21 2021-10-29 Hexima Ltd A method of treatment of fungal infections
EP3739058B1 (en) 2015-03-30 2023-07-26 Amtixbio Co., Ltd. Novel gene regulating virulence of cryptococcus neoformans, and use thereof
KR101683002B1 (en) * 2015-07-03 2016-12-07 배재대학교 산학협력단 USE OF sppA GENE AND SppA PROTEIN FOR TREATMENT OF ASPERGILLOSIS
DK3487873T3 (en) * 2016-07-22 2021-05-25 Novozymes As Improved filamentous fungal host
KR20160117380A (en) 2016-07-25 2016-10-10 (주)앰틱스바이오 Novel genes for regulating the virulence of Cryptococcus neoformans and their use
KR20160118162A (en) 2016-07-25 2016-10-11 (주)앰틱스바이오 Novel target genes for anti-fungal agent of Cryptococcus neoformans and their use
KR20170078561A (en) 2017-05-23 2017-07-07 (주)앰틱스바이오 Novel genes for regulating the virulence of Cryptococcus neoformans and their use
CN107308178B (en) * 2017-07-31 2020-11-10 苏州大学附属儿童医院 A drug for parenteral nutrition-related liver disease
US20230296613A1 (en) * 2019-09-18 2023-09-21 Amtixbio Co., Ltd. Use of gene involved in passage through brain-blood barrier and survival inside brain of causative fungi of meningoencephalitis

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
BACK, S. H. ET AL.: "ER stress signaling by regulated splicing: IRE1/HAC1/XBP1", METHODS., vol. 35, no. 4, April 2005 (2005-04-01), pages 395 - 416, XP004813160, DOI: doi:10.1016/j.ymeth.2005.03.001 *
CHEON, S. A. ET AL.: "Unique evolution of the UPR pathway with a novel bZIP transcription factor, Hxll, for controlling pathogenicity of Cryptococcus neoformans", PLOS PATHOGENS., vol. 7, no. 8, 11 August 2011 (2011-08-11), pages E1002177 *
FAN, W. ET AL.: "Ecal, a sarcoplasmic/endoplasmic reticulum Ca2+-ATPase, is involved in stress tolerance and virulence in Cryptococcus neoformans", INFECTION AND IMMUNITY., vol. 75, no. 7, 14 May 2007 (2007-05-14), pages 3394 - 3405 *
HU, G. ET AL.: "A putative P-type ATPase, Aptl, is involved in stress tolerance and virulence in Cryptococcus neoformans", EUKARYOTIC CELL., vol. 9, no. 1, 30 November 2009 (2009-11-30), pages 74 - 83 *
MAENG, S. ET AL.: "Comparative transcriptome analysis reveals novel roles of the Ras and cyclic AMP signaling pathways in environmental stress response and antifungal drug sensitivity in Cryptococcus neoformans", EUKARYOTIC CELL., vol. 9, no. 3, 22 January 2010 (2010-01-22), pages 360 - 378 *

Also Published As

Publication number Publication date
KR101311196B1 (en) 2013-09-27
WO2012087004A2 (en) 2012-06-28
KR20120072096A (en) 2012-07-03

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