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Metzenmacher, M. ; Váraljai, R. ; Hegedüs, B. ; Klein, Christoph A. ; ; ; ; ; ; ; ; ; ; ; ; ; ; ;

Plasma next generation sequencing and droplet digital-qPCR-based quantification of circulating cell-free RNA for noninvasive early detection of cancer

Artikel

Metzenmacher, M., Váraljai, R. , Hegedüs, B., Klein, Christoph A., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference (2020) Plasma next generation sequencing and droplet digital-qPCR-based quantification of circulating cell-free RNA for noninvasive early detection of cancer. Cancers 12, S. 353.

DOI zum Zitieren dieses Dokuments: 10.5283/epub.41569


Zusammenfassung

Early detection of cancer holds high promise for reducing cancer-related mortality. Detection of circulating tumor-specific nucleic acids holds promise, but sensitivity and specificity issues remain with current technology. We studied cell-free RNA (cfRNA) in patients with non-small cell lung cancer (NSCLC; n = 56 stage IV, n = 39 stages I-III), pancreatic cancer (PDAC, n = 20 stage III), ...

Early detection of cancer holds high promise for reducing cancer-related mortality. Detection of circulating tumor-specific nucleic acids holds promise, but sensitivity and specificity issues remain with current technology. We studied cell-free RNA (cfRNA) in patients with non-small cell lung cancer (NSCLC; n = 56 stage IV, n = 39 stages I-III), pancreatic cancer (PDAC, n = 20 stage III), malignant melanoma (MM, n = 12 stage III-IV), urothelial bladder cancer (UBC, n = 22 stage II and IV), and 65 healthy controls by means of next generation sequencing (NGS) and real-time droplet digital PCR (RT-ddPCR). We identified 192 overlapping upregulated transcripts in NSCLC and PDAC by NGS, more than 90% of which were noncoding. Previously reported transcripts (e.g., HOTAIRM1) were identified. Plasma cfRNA transcript levels of POU6F2-AS2 discriminated NSCLC from healthy donors (AUC = 0.82 and 0.76 for stages IV and I-III, respectively) and significantly associated (p = 0.017) with the established tumor marker Cyfra 21-1. cfRNA yield and POU6F2-AS transcript abundance discriminated PDAC patients from healthy donors (AUC = 1.0). POU6F2-AS2 transcript was significantly higher in MM (p = 0.044). In summary, our findings support further validation of cfRNA detection by RT-ddPCR as a biomarker for early detection of solid cancers.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftCancers
VerlagMDPI
Ort der VeröffentlichungBASEL
Band12
SeitenbereichS. 353
Datum4 Februar 2020
Veröffentlichungsdatum12 Feb 2020 15:12
InstitutionenMedizin > Lehrstuhl für experimentelle Medizin und Therapieverfahren
Identifikationsnummer
WertTyp
10.3390/cancers12020353DOI
Stichwörter / KeywordsMESSENGER-RNA; LUNG-CANCER; POTENTIAL BIOMARKER; COLORECTAL-CANCER; SERUM; DIAGNOSIS; PROGNOSIS; CLASSIFIER; GEFITINIB; MORTALITY; liquid biopsy; cfRNA; cancer; ddPCR; NGS; POU6F2-AS2; early detection
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenZum Teil
URN der UB Regensburgurn:nbn:de:bvb:355-epub-415691
Dokumenten-ID41569

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