Failure, Success, and Future Direction of Alzheimer Drugs Targeting Amyloid-β Cascade: Pros and Cons of Chemical and Biological Modalities
Alzheimer's disease (AD) is the most prevalent cause of dementia and has become a health concern worldwide urging for an effective therapeutic. The amyloid hypothesis, currently the most pursued basis of AD drug discovery, points the cause of AD to abnormal production and ineffective removal of...
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Veröffentlicht in: | Chembiochem : a European journal of chemical biology 2023-10, Vol.24 (19), p.e202300328-e202300328 |
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creator | Kim, JiMin Jeon, Hanna Yun Kim, Hye Kim, YoungSoo |
description | Alzheimer's disease (AD) is the most prevalent cause of dementia and has become a health concern worldwide urging for an effective therapeutic. The amyloid hypothesis, currently the most pursued basis of AD drug discovery, points the cause of AD to abnormal production and ineffective removal of pathogenic aggregated amyloid-β (Aβ). AD therapeutic research has been focused on targeting different species of Aβ in the amyloidogenic process to control Aβ content and recover cognitive decline. Among the different processes targeted, the clearance mechanism has been found to be the most effective, supported by the recent clinical approval of an Aβ-targeting immunotherapeutic drug which significantly slowed cognitive decline. Although the current AD drug discovery field is extensively researching immunotherapeutic drugs, there are numerous properties of immunotherapy in need of improvements that could be overcome by an equally performing chemical drug. Here, we review chemical and immunotherapy drug candidates, based on their mechanism of modulating the amyloid cascade, selected from the AlzForum database. Through this review, we aim to summarize and evaluate the prospect of Aβ-targeting chemical drugs. |
doi_str_mv | 10.1002/cbic.202300328 |
format | Article |
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The amyloid hypothesis, currently the most pursued basis of AD drug discovery, points the cause of AD to abnormal production and ineffective removal of pathogenic aggregated amyloid-β (Aβ). AD therapeutic research has been focused on targeting different species of Aβ in the amyloidogenic process to control Aβ content and recover cognitive decline. Among the different processes targeted, the clearance mechanism has been found to be the most effective, supported by the recent clinical approval of an Aβ-targeting immunotherapeutic drug which significantly slowed cognitive decline. Although the current AD drug discovery field is extensively researching immunotherapeutic drugs, there are numerous properties of immunotherapy in need of improvements that could be overcome by an equally performing chemical drug. Here, we review chemical and immunotherapy drug candidates, based on their mechanism of modulating the amyloid cascade, selected from the AlzForum database. Through this review, we aim to summarize and evaluate the prospect of Aβ-targeting chemical drugs.</description><identifier>ISSN: 1439-4227</identifier><identifier>EISSN: 1439-7633</identifier><identifier>DOI: 10.1002/cbic.202300328</identifier><identifier>PMID: 37497809</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alzheimer's disease ; Amyloidogenesis ; Cognitive ability ; Dementia disorders ; Drug delivery ; Drug development ; Drug discovery ; Drugs ; Immunotherapy ; Neurodegenerative diseases ; β-Amyloid</subject><ispartof>Chembiochem : a European journal of chemical biology, 2023-10, Vol.24 (19), p.e202300328-e202300328</ispartof><rights>2023 Wiley-VCH Verlag GmbH.</rights><rights>2023 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-dbe7f4e90d26946d971e545932292d2cc684279a31cc310a2a5d6833c789d49d3</citedby><cites>FETCH-LOGICAL-c323t-dbe7f4e90d26946d971e545932292d2cc684279a31cc310a2a5d6833c789d49d3</cites><orcidid>0000-0001-5029-7082</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37497809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, JiMin</creatorcontrib><creatorcontrib>Jeon, Hanna</creatorcontrib><creatorcontrib>Yun Kim, Hye</creatorcontrib><creatorcontrib>Kim, YoungSoo</creatorcontrib><title>Failure, Success, and Future Direction of Alzheimer Drugs Targeting Amyloid-β Cascade: Pros and Cons of Chemical and Biological Modalities</title><title>Chembiochem : a European journal of chemical biology</title><addtitle>Chembiochem</addtitle><description>Alzheimer's disease (AD) is the most prevalent cause of dementia and has become a health concern worldwide urging for an effective therapeutic. 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Through this review, we aim to summarize and evaluate the prospect of Aβ-targeting chemical drugs.</description><subject>Alzheimer's disease</subject><subject>Amyloidogenesis</subject><subject>Cognitive ability</subject><subject>Dementia disorders</subject><subject>Drug delivery</subject><subject>Drug development</subject><subject>Drug discovery</subject><subject>Drugs</subject><subject>Immunotherapy</subject><subject>Neurodegenerative diseases</subject><subject>β-Amyloid</subject><issn>1439-4227</issn><issn>1439-7633</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkcFOGzEQhq2KqgHaa4_IEpce2NTrcdZrbulCaCWqIkHPK8eeJI68a7B3D_AKvA0PwjOxCWkOPc3Mr29-zegn5GvOxjlj_LuZOzPmjANjwMsP5DAXoDJZABzsesG5HJGjlNaMMVVA_omMQAolS6YOyfNMO99HPKO3vTGY0hnVraWzvhtEeuEims6FloYFnfqnFboGI72I_TLROx2X2Ll2SafNow_OZq8vtNLJaIvn9CaGtLWqQps269UKG2e034o_XPBhuR1_B6u96xymz-TjQvuEX3b1mPydXd5VP7PrP1e_qul1ZoBDl9k5yoVAxSwvlCiskjlOxEQB54pbbkxRCi6VhtwYyJnmemKLEsDIUlmhLByTb---9zE89Ji6unHJoPe6xdCnmpcCGAihJgN6-h-6Dn1sh-sGSoqiKLncUON3ygxPp4iL-j66RsfHOmf1JqZ6E1O9j2lYONnZ9vMG7R7_lwu8AakIjZI</recordid><startdate>20231004</startdate><enddate>20231004</enddate><creator>Kim, JiMin</creator><creator>Jeon, Hanna</creator><creator>Yun Kim, Hye</creator><creator>Kim, YoungSoo</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5029-7082</orcidid></search><sort><creationdate>20231004</creationdate><title>Failure, Success, and Future Direction of Alzheimer Drugs Targeting Amyloid-β Cascade: Pros and Cons of Chemical and Biological Modalities</title><author>Kim, JiMin ; Jeon, Hanna ; Yun Kim, Hye ; Kim, YoungSoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-dbe7f4e90d26946d971e545932292d2cc684279a31cc310a2a5d6833c789d49d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alzheimer's disease</topic><topic>Amyloidogenesis</topic><topic>Cognitive ability</topic><topic>Dementia disorders</topic><topic>Drug delivery</topic><topic>Drug development</topic><topic>Drug discovery</topic><topic>Drugs</topic><topic>Immunotherapy</topic><topic>Neurodegenerative diseases</topic><topic>β-Amyloid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, JiMin</creatorcontrib><creatorcontrib>Jeon, Hanna</creatorcontrib><creatorcontrib>Yun Kim, Hye</creatorcontrib><creatorcontrib>Kim, YoungSoo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chembiochem : a European journal of chemical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, JiMin</au><au>Jeon, Hanna</au><au>Yun Kim, Hye</au><au>Kim, YoungSoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Failure, Success, and Future Direction of Alzheimer Drugs Targeting Amyloid-β Cascade: Pros and Cons of Chemical and Biological Modalities</atitle><jtitle>Chembiochem : a European journal of chemical biology</jtitle><addtitle>Chembiochem</addtitle><date>2023-10-04</date><risdate>2023</risdate><volume>24</volume><issue>19</issue><spage>e202300328</spage><epage>e202300328</epage><pages>e202300328-e202300328</pages><issn>1439-4227</issn><eissn>1439-7633</eissn><abstract>Alzheimer's disease (AD) is the most prevalent cause of dementia and has become a health concern worldwide urging for an effective therapeutic. The amyloid hypothesis, currently the most pursued basis of AD drug discovery, points the cause of AD to abnormal production and ineffective removal of pathogenic aggregated amyloid-β (Aβ). AD therapeutic research has been focused on targeting different species of Aβ in the amyloidogenic process to control Aβ content and recover cognitive decline. Among the different processes targeted, the clearance mechanism has been found to be the most effective, supported by the recent clinical approval of an Aβ-targeting immunotherapeutic drug which significantly slowed cognitive decline. Although the current AD drug discovery field is extensively researching immunotherapeutic drugs, there are numerous properties of immunotherapy in need of improvements that could be overcome by an equally performing chemical drug. Here, we review chemical and immunotherapy drug candidates, based on their mechanism of modulating the amyloid cascade, selected from the AlzForum database. 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source | Wiley Online Library Journals Frontfile Complete |
subjects | Alzheimer's disease Amyloidogenesis Cognitive ability Dementia disorders Drug delivery Drug development Drug discovery Drugs Immunotherapy Neurodegenerative diseases β-Amyloid |
title | Failure, Success, and Future Direction of Alzheimer Drugs Targeting Amyloid-β Cascade: Pros and Cons of Chemical and Biological Modalities |
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