Exosomal RNA-profiling of pleural effusions identifies adenocarcinoma patients through elevated miR-200 and LCN2 expression. (October 2018)
- Record Type:
- Journal Article
- Title:
- Exosomal RNA-profiling of pleural effusions identifies adenocarcinoma patients through elevated miR-200 and LCN2 expression. (October 2018)
- Main Title:
- Exosomal RNA-profiling of pleural effusions identifies adenocarcinoma patients through elevated miR-200 and LCN2 expression
- Authors:
- Hydbring, Per
De Petris, Luigi
Zhang, Yanming
Brandén, Eva
Koyi, Hirsh
Novak, Metka
Kanter, Lena
Hååg, Petra
Hurley, James
Tadigotla, Vasisht
Zhu, Baoli
Skog, Johan
Viktorsson, Kristina
Ekman, Simon
Lewensohn, Rolf - Abstract:
- Highlights: Pleural effusions provide an abundant source for liquid biopsy RNA-profiling. Exosomal derived microRNAs provide superior diagnostic value compared to mRNAs. Specific exosomal derived RNAs define patients with lung adenocarcinoma. Abstract: Hypothesis: The inherent challenges associated with tissue biopsies from lung have spurred an interest in the use of liquid biopsies. Pleural effusions are one source of liquid biopsy. Recently, extracellular vesicles of endocytic origin, exosomes, have attracted interest as liquid biopsy of tumors as they are thought to be a mirror of their tumor of origin. Here, we aimed to analyze if RNA profiling of exosomes isolated from pleural effusions could differentiate patients with lung adenocarcinoma from patients with benign inflammatory processes. Methods: Exosomes were isolated from 36 pleural effusions from patients with adenocarcinoma (n = 18) and patients with benign inflammatory processes (n = 18). The two groups were balanced with respect to age and smoking history but with a gender bias towards males in the benign group. Profiling was conducted using RT-qPCR arrays covering 754 microRNAs and 624 mRNAs followed by statistical ranking of differentially regulated transcripts between the two patient cohorts. Results: RNA profiling revealed differential expression of 17 microRNAs and 71 mRNAs in pleural effusions collected from patients with lung adenocarcinoma compared to pleural effusions from benign lung disease. Overall,Highlights: Pleural effusions provide an abundant source for liquid biopsy RNA-profiling. Exosomal derived microRNAs provide superior diagnostic value compared to mRNAs. Specific exosomal derived RNAs define patients with lung adenocarcinoma. Abstract: Hypothesis: The inherent challenges associated with tissue biopsies from lung have spurred an interest in the use of liquid biopsies. Pleural effusions are one source of liquid biopsy. Recently, extracellular vesicles of endocytic origin, exosomes, have attracted interest as liquid biopsy of tumors as they are thought to be a mirror of their tumor of origin. Here, we aimed to analyze if RNA profiling of exosomes isolated from pleural effusions could differentiate patients with lung adenocarcinoma from patients with benign inflammatory processes. Methods: Exosomes were isolated from 36 pleural effusions from patients with adenocarcinoma (n = 18) and patients with benign inflammatory processes (n = 18). The two groups were balanced with respect to age and smoking history but with a gender bias towards males in the benign group. Profiling was conducted using RT-qPCR arrays covering 754 microRNAs and 624 mRNAs followed by statistical ranking of differentially regulated transcripts between the two patient cohorts. Results: RNA profiling revealed differential expression of 17 microRNAs and 71 mRNAs in pleural effusions collected from patients with lung adenocarcinoma compared to pleural effusions from benign lung disease. Overall, top differentially expressed microRNAs, including miR-200 family microRNAs, provided a stronger diagnostic power compared to top differentially expressed mRNAs. However, the mRNA transcript encoding Lipocalin-2 (LCN2) displayed the strongest diagnostic power of all analyzed transcripts (AUC: 0.9916). Conclusions: Our study demonstrates that exosomal RNA profiling from pleural effusions can be used to identify patients with lung adenocarcinoma from individuals with benign processes and further proposes miR-200 microRNAs and LCN2 as diagnostic markers in lung cancer liquid biopsies. … (more)
- Is Part Of:
- Lung cancer. Volume 124(2018)
- Journal:
- Lung cancer
- Issue:
- Volume 124(2018)
- Issue Display:
- Volume 124, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 124
- Issue:
- 2018
- Issue Sort Value:
- 2018-0124-2018-0000
- Page Start:
- 45
- Page End:
- 52
- Publication Date:
- 2018-10
- Subjects:
- Exosomes -- Pleural effusions -- microRNAs -- mRNAs -- Lung adenocarcinomas
Lungs -- Cancer -- Periodicals
Lung Neoplasms -- Abstracts
Lung Neoplasms -- Periodicals
Poumons -- Cancer -- Périodiques
Lungs -- Cancer
Periodicals
Electronic journals
Electronic journals
616.99424 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01695002 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01695002 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01695002 ↗
http://www.lungcancerjournal.info/issues ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lungcan.2018.07.018 ↗
- Languages:
- English
- ISSNs:
- 0169-5002
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5307.245000
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