Efficient discovery of anticancer peptides via cost-aware ranking learning

preprint OA: closed CC-BY-4.0
📄 Open PDF Full text JSON View at publisher
AI-generated summary by claude@2026-06, 2026-06-23

This paper presents a cost-aware ranking learning method for efficiently discovering anticancer peptides by optimizing both prediction accuracy and cost considerations.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-23 · read from full text

The preprint presents ACPRank, a computational framework for discovering potent anticancer peptides by using cost-aware ranking learning with a unified activity scoring system built from multidimensional pharmacological metrics and a customized ranking loss that targets high-activity candidates under resource-limited screening. Using systematic screening of the human secretome, the authors report identification of two novel human-derived ACPs (DRP and KRP) with broad-spectrum antitumor activity in vitro and in vivo and a favorable safety profile. Mechanistic work for KRP indicates marked cell cycle arrest via downregulation of mitotic regulators including AURKB, BUB1, CCNB1, and NCAPH. A key caveat explicitly stated is that the work is a preprint and has not been peer reviewed by a journal. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Full text 13,690 characters · extracted from preprint-html · click to expand
Efficient discovery of anticancer peptides via cost-aware ranking learning | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Article Efficient discovery of anticancer peptides via cost-aware ranking learning Ying Wang, Jianda Yue, Jiawei Xu, Zihui Chen, Tingting Li, Zhaoyang Tang, and 4 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-8539436/v1 This work is licensed under a CC BY 4.0 License Status: Under Review Version 1 posted You are reading this latest preprint version Abstract While anticancer peptides (ACPs) have emerged as a promising class of next-generation therapeutics, efficiently identifying potent candidates across the vast peptide sequence space remains a pressing challenge. Here, we present ACPRank, a computational framework based on cost-aware ranking learning tailored for discovering potent ACPs. By integrating a unified activity scoring system encompassing multidimensional pharmacological metrics and employing a customized ranking loss, the framework directly embeds the core objective of targeting high-activity candidates under resource-limited conditions into the optimization process, thereby enabling precise candidate prioritization. Systematic screening of the human secretome facilitated the identification of two novel human-derived ACPs (termed DRP and KRP), both of which exhibited robust broad-spectrum antitumor efficacy in vitro and in vivo , alongside a favorable safety profile. Mechanistic investigations revealed that KRP induces marked cell cycle arrest by downregulating key mitotic regulators, including Aurora Kinase B (AURKB), Budding Uninhibited by Benzimidazoles 1 (BUB1), Cyclin B1 (CCNB1), and Non-SMC Condensin I Complex Subunit H (NCAPH). Overall, ACPRank enables rapid identification of highly active candidates and thus holds great potential for addressing the efficiency bottleneck in large-scale peptide screening. Biological sciences/Computational biology and bioinformatics/Machine learning Biological sciences/Computational biology and bioinformatics/Virtual drug screening Biological sciences/Cancer/Cancer therapy/Drug development Biological sciences/Drug discovery/Drug screening/Virtual screening Biological sciences/Biochemistry/Peptides anticancer peptide ACPRank ranking learning cell cycle human secretome Full Text Additional Declarations There is NO Competing Interest. Supplementary Files SupplementaryInformation.pdf Supplementary Information Cite Share Download PDF Status: Under Review Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-8539436","acceptedTermsAndConditions":true,"allowDirectSubmit":false,"archivedVersions":[],"articleType":"Article","associatedPublications":[],"authors":[{"id":573897999,"identity":"4a378e3d-2ebc-4a6a-9824-de5b3bc78326","order_by":0,"name":"Ying Wang","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAA10lEQVRIiWNgGAWjYNACAwY5AyiTsYFYLcakamFgSNxAtBaD42cPv+YpuJO+XSL32GMeBhvZDQeYnz3Aq+VMXpo1j8Gz3J0z8tKNeRjSjDccYDM3wKfF7ECOmTGPweHcDTdyzKR5GA4nbjjAwyaBV8v5N2At6QYQLf+J0HIjx/gxUEsCVMsBwlrsb7wxY5xjcNhww5k3ZpJzDJKNZx5mM8OrRbI/x/jDmz+H5Q2O55hJvKmwk+073vwMrxYgYJPigbNBQcVMQD1IyccfhBWNglEwCkbBSAYABMlIcLGBYYEAAAAASUVORK5CYII=","orcid":"https://orcid.org/0000-0002-4359-3753","institution":"Hunan Normal University","correspondingAuthor":true,"prefix":"","firstName":"Ying","middleName":"","lastName":"Wang","suffix":""},{"id":573898000,"identity":"291e200b-9b20-44f2-8007-c85563a77a4a","order_by":1,"name":"Jianda Yue","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Jianda","middleName":"","lastName":"Yue","suffix":""},{"id":573898001,"identity":"e69bacfc-30f7-408f-b658-0b76087e7f13","order_by":2,"name":"Jiawei Xu","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Jiawei","middleName":"","lastName":"Xu","suffix":""},{"id":573898002,"identity":"12d29fe1-e2a4-4933-ab6b-ffcd87754ff7","order_by":3,"name":"Zihui Chen","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Zihui","middleName":"","lastName":"Chen","suffix":""},{"id":573898003,"identity":"9a0c349f-58ed-407f-8c0a-85c8f44b588a","order_by":4,"name":"Tingting Li","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Tingting","middleName":"","lastName":"Li","suffix":""},{"id":573898004,"identity":"c0bf5154-c6ff-4ccd-b818-2d24448aac51","order_by":5,"name":"Zhaoyang Tang","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Zhaoyang","middleName":"","lastName":"Tang","suffix":""},{"id":573898005,"identity":"fcb2023b-9091-4be5-8b82-535190748a80","order_by":6,"name":"Xie Li","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Xie","middleName":"","lastName":"Li","suffix":""},{"id":573898006,"identity":"6a5dc8a3-6083-49f7-8c32-a37ce597629c","order_by":7,"name":"Hua Tan","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Hua","middleName":"","lastName":"Tan","suffix":""},{"id":573898007,"identity":"b1c26d58-28cb-4aea-bce1-4e3ac5aa3739","order_by":8,"name":"Wangfei Xiang","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Wangfei","middleName":"","lastName":"Xiang","suffix":""},{"id":573898008,"identity":"4c508eec-e7eb-4702-aa94-9d7239cd7c73","order_by":9,"name":"Zhonghua Liu","email":"","orcid":"","institution":"Hunan Normal University","correspondingAuthor":false,"prefix":"","firstName":"Zhonghua","middleName":"","lastName":"Liu","suffix":""}],"badges":[],"createdAt":"2026-01-07 09:35:35","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-8539436/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-8539436/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":101298134,"identity":"1752eea1-c97d-49bd-98df-070078cc0bb3","added_by":"auto","created_at":"2026-01-28 09:30:41","extension":"pdf","order_by":1,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":1123542,"visible":true,"origin":"","legend":"","description":"","filename":"ACPRankManuscript01072.pdf","url":"https://assets-eu.researchsquare.com/files/rs-8539436/v1_covered_d529f679-72f3-4954-b2d5-7dd5be9dc6c3.pdf"},{"id":101284641,"identity":"53d415e8-5ae2-4b98-9b27-6c746ca9d617","added_by":"auto","created_at":"2026-01-28 06:14:18","extension":"pdf","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":6901467,"visible":true,"origin":"","legend":"Supplementary Information","description":"","filename":"SupplementaryInformation.pdf","url":"https://assets-eu.researchsquare.com/files/rs-8539436/v1/8652bf7ad663b193835ba6d6.pdf"}],"financialInterests":"There is \u003cb\u003eNO\u003c/b\u003e Competing Interest.","formattedTitle":"Efficient discovery of anticancer peptides via cost-aware ranking learning","fulltext":[],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":false,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":true,"hideJournal":false,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":true,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":true,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"nature-portfolio","isNatureJournal":true,"hasQc":false,"allowDirectSubmit":false,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"","title":"Nature Portfolio","twitterHandle":"","acdcEnabled":false,"dfaEnabled":false,"editorialSystem":"ejp","reportingPortfolio":"","inReviewEnabled":true,"inReviewRevisionsEnabled":false},"keywords":"anticancer peptide, ACPRank, ranking learning, cell cycle, human secretome","lastPublishedDoi":"10.21203/rs.3.rs-8539436/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-8539436/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003eWhile anticancer peptides (ACPs) have emerged as a promising class of next-generation therapeutics, efficiently identifying potent candidates across the vast peptide sequence space remains a pressing challenge. Here, we present ACPRank, a computational framework based on cost-aware ranking learning tailored for discovering potent ACPs. By integrating a unified activity scoring system encompassing multidimensional pharmacological metrics and employing a customized ranking loss, the framework directly embeds the core objective of targeting high-activity candidates under resource-limited conditions into the optimization process, thereby enabling precise candidate prioritization. Systematic screening of the human secretome facilitated the identification of two novel human-derived ACPs (termed DRP and KRP), both of which exhibited robust broad-spectrum antitumor efficacy \u003cem\u003ein vitro\u003c/em\u003e and \u003cem\u003ein vivo\u003c/em\u003e, alongside a favorable safety profile. Mechanistic investigations revealed that KRP induces marked cell cycle arrest by downregulating key mitotic regulators, including Aurora Kinase B (AURKB), Budding Uninhibited by Benzimidazoles 1 (BUB1), Cyclin B1 (CCNB1), and Non-SMC Condensin I Complex Subunit H (NCAPH). Overall, ACPRank enables rapid identification of highly active candidates and thus holds great potential for addressing the efficiency bottleneck in large-scale peptide screening.\u003c/p\u003e","manuscriptTitle":"Efficient discovery of anticancer peptides via cost-aware ranking learning","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2026-01-28 06:14:13","doi":"10.21203/rs.3.rs-8539436/v1","editorialEvents":[],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"nature-communications","isNatureJournal":true,"hasQc":false,"allowDirectSubmit":false,"externalIdentity":"NCOMMS","sideBox":"Learn more about [Nature Communications](http://www.nature.com/ncomms/)","snPcode":"","submissionUrl":"https://mts-ncomms.nature.com/","title":"Nature Communications","twitterHandle":"","acdcEnabled":true,"dfaEnabled":true,"editorialSystem":"ejp","reportingPortfolio":"Nature Communications","inReviewEnabled":true,"inReviewRevisionsEnabled":false}}],"origin":"","ownerIdentity":"022307ca-3269-4977-94c2-659c86c394bd","owner":[],"postedDate":"January 28th, 2026","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"under-review","subjectAreas":[{"id":61064096,"name":"Biological sciences/Computational biology and bioinformatics/Machine learning"},{"id":61064097,"name":"Biological sciences/Computational biology and bioinformatics/Virtual drug screening"},{"id":61064098,"name":"Biological sciences/Cancer/Cancer therapy/Drug development"},{"id":61064099,"name":"Biological sciences/Drug discovery/Drug screening/Virtual screening"},{"id":61064100,"name":"Biological sciences/Biochemistry/Peptides"}],"tags":[],"updatedAt":"2026-01-28T06:14:13+00:00","versionOfRecord":[],"versionCreatedAt":"2026-01-28 06:14:13","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-8539436","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-8539436","identity":"rs-8539436","version":["v1"]},"buildId":"XKTyCvWXoU3ODBz1xrDgd","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: preprint-html

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (sparse)

Too few in-corpus citations on either side for a chart; here are the lists.

Cites (1)

References (62)

Source provenance

crossref
last seen: 2026-06-22T06:34:23.099224+00:00
europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-22T02:00:06.705733+00:00
License: CC-BY-4.0