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The value of circulating microRNAs for early diagnosis of B-cell lymphoma: A case-control study on historical samples.

Steffen JørgensenIsabella Worlewenut PaulsenJakob Werner HansenDorte TholstrupChristoffer HotherErik SørensenMikkel Steen PetersenKaspar Rene NielsenKlaus RostgaardMargit Anita Hørup LarsenPeter de Nully BrownElisabeth RalfkiærKeld Mikkelsen HomburgHenrik HjalgrimChristian ErikstrupHenrik UllumJesper Thorvald TroelsenKirsten GrønbækOle Birger Pedersen
Published in: Scientific reports (2020)
MicroRNAs are small regulatory RNAs that are deregulated in a wide variety of human cancers, including different types of B-cell lymphoma. Nevertheless, the feasibility of circulating microRNA for early diagnosis of B-cell lymphoma has not been established. To address the possibility of detecting specific circulating microRNAs years before a B-cell lymphoma is diagnosed, we studied the plasma expression of microRNA first in pre-treatment samples from patients with diffuse large B-cell lymphoma and subsequently in repository samples from blood donors who later developed B-cell lymphomas. In addition, we studied the microRNA expression in the diagnostic lymphoma biopsy. The most strongly induced (miR-326) and suppressed (miR-375) plasma microRNA at diagnosis, when compared with healthy blood donors, were also substantially up- or down-regulated in plasma repository samples taken from several months to up to two years before the blood donors were diagnosed with B-cell lymphoma. Importantly, at these time points the donors had no signs of disease and felt healthy enough to donate blood. In conclusion, this first study of plasma microRNA profiles from apparently healthy individuals, taken several years before B-cell lymphoma diagnosis, suggests that plasma microRNA profiles may be predictive of lymphoma development.
Keyphrases
  • diffuse large b cell lymphoma
  • epstein barr virus
  • poor prognosis
  • long non coding rna
  • binding protein
  • young adults
  • ultrasound guided
  • combination therapy
  • diabetic rats
  • pluripotent stem cells