Ultrasensitive detection of circulating LINE-1 ORF1p as a specific multi-cancer biomarker.
Martin S TaylorConnie WuPeter C FridyYasmeen SenussiWen-Chih ChengJohn HeapsKei MoriLimor CohenKelly R MolloyBrian T ChaitMichael GogginsIrun BhanJoseph W FransesXiaoyu YangMary-Ellen TaplinXinan WangDavid C ChristianiBruce E JohnsonMatthew MeyersonRavindra UppaluriAnn Marie EgloffElyssa N DenaultLaura M SpringTian-Li WangIe-Ming ShihEuihye JungKshitij S AroraLawrence R ZukerbergOsman H YilmazGary ChiBryanna L NordenYuhui SongLinda NiemanAparna R ParikhMatthew StricklandTomas MustelinGeorge EngÖmer H YilmazUrsula A MatulonisSteven J SkatesBo R RuedaRonny DrapkinSamuel J KlempnerVikram DeshpandeDavid T TingMichael P RoutJohn LaCavaDavid R WaltKathleen H BurnsPublished in: bioRxiv : the preprint server for biology (2023)
Improved biomarkers are needed for early cancer detection, risk stratification, treatment selection, and monitoring treatment response. While proteins can be useful blood-based biomarkers, many have limited sensitivity or specificity for these applications. Long INterspersed Element-1 (LINE-1, L1) open reading frame 1 protein (ORF1p) is a transposable element protein overexpressed in carcinomas and high-risk precursors during carcinogenesis with negligible detectable expression in corresponding normal tissues, suggesting ORF1p could be a highly specific cancer biomarker. To explore the potential of ORF1p as a blood-based biomarker, we engineered ultrasensitive digital immunoassays that detect mid-attomolar (10 -17 M) ORF1p concentrations in patient plasma samples across multiple cancers with high specificity. Plasma ORF1p shows promise for early detection of ovarian cancer, improves diagnostic performance in a multi-analyte panel, and provides early therapeutic response monitoring in gastric and esophageal cancers. Together, these observations nominate ORF1p as a multi-cancer biomarker with potential utility for disease detection and monitoring.
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