Abbi Abdel-Rehim, Oghenejokpeme Orhobor, Gareth Griffiths, Larisa Soldatova, Ross D. King
{"title":"Personalised Medicine: Establishing predictive machine learning models for drug responses in patient derived cell culture","authors":"Abbi Abdel-Rehim, Oghenejokpeme Orhobor, Gareth Griffiths, Larisa Soldatova, Ross D. King","doi":"arxiv-2408.13012","DOIUrl":null,"url":null,"abstract":"The concept of personalised medicine in cancer therapy is becoming\nincreasingly important. There already exist drugs administered specifically for\npatients with tumours presenting well-defined mutations. However, the field is\nstill in its infancy, and personalised treatments are far from being standard\nof care. Personalised medicine is often associated with the utilisation of\nomics data. Yet, implementation of multi-omics data has proven difficult, due\nto the variety and scale of the information within the data, as well as the\ncomplexity behind the myriad of interactions taking place within the cell. An\nalternative approach to precision medicine is to employ a function-based\nprofile of the cell. This involves screening a range of drugs against patient\nderived cells. Here we demonstrate a proof-of-concept, where a collection of\ndrug screens against a highly diverse set of patient-derived cell lines, are\nleveraged to identify putative treatment options for a 'new patient'. We show\nthat this methodology is highly efficient in ranking the drugs according to\ntheir activity towards the target cells. We argue that this approach offers\ngreat potential, as activities can be efficiently imputed from various subsets\nof the drug treated cell lines that do not necessarily originate from the same\ntissue type.","PeriodicalId":501022,"journal":{"name":"arXiv - QuanBio - Biomolecules","volume":"39 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Biomolecules","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2408.13012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The concept of personalised medicine in cancer therapy is becoming
increasingly important. There already exist drugs administered specifically for
patients with tumours presenting well-defined mutations. However, the field is
still in its infancy, and personalised treatments are far from being standard
of care. Personalised medicine is often associated with the utilisation of
omics data. Yet, implementation of multi-omics data has proven difficult, due
to the variety and scale of the information within the data, as well as the
complexity behind the myriad of interactions taking place within the cell. An
alternative approach to precision medicine is to employ a function-based
profile of the cell. This involves screening a range of drugs against patient
derived cells. Here we demonstrate a proof-of-concept, where a collection of
drug screens against a highly diverse set of patient-derived cell lines, are
leveraged to identify putative treatment options for a 'new patient'. We show
that this methodology is highly efficient in ranking the drugs according to
their activity towards the target cells. We argue that this approach offers
great potential, as activities can be efficiently imputed from various subsets
of the drug treated cell lines that do not necessarily originate from the same
tissue type.