Proteomics

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Circulating Microvesicles and Exosomes in Small Cell Lung Cancer by Quantitative Proteomics


ABSTRACT: Early detection of small cell lung cancer crucially demands highly reliable markers. Growing evidence suggests that extracellular vesicles carry tumor cell-specific cargo suitable as protein markers in cancer. Therefore, we isolated plasma-derived microvesicles from newly diagnosed small cell lung cancer patients and investigated proteome dynamics of these microvesicles aiming at improving the detection of small cell lung cancer. A total of 1,223 proteins were initially identified. After data processing and statistical analysis, several proteins were found to be differentially expressed in comparing small cell lung cancer patients and healthy individuals. Furthermore, our data may indicate involvement of complement activation, integrin-mediated signaling, cell adhesion- and migration, and blood coagulation in small cell lung cancer pathogenesis.

INSTRUMENT(S): Orbitrap Fusion

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Plasma

DISEASE(S): Lung Cancer

SUBMITTER: Bent Honoré  

LAB HEAD: Bent Honoré

PROVIDER: PXD028944 | Pride | 2022-04-04

REPOSITORIES: Pride

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Publications

Circulating microvesicles and exosomes in small cell lung cancer by quantitative proteomics.

Pedersen Shona S   Jensen Katrine Papendick KP   Honoré Bent B   Kristensen Søren Risom SR   Pedersen Camilla Holm CH   Szejniuk Weronika Maria WM   Maltesen Raluca Georgiana RG   Falkmer Ursula U  

Clinical proteomics 20220107 1


<h4>Background</h4>Early detection of small cell lung cancer (SCLC) crucially demands highly reliable markers. Growing evidence suggests that extracellular vesicles carry tumor cell-specific cargo suitable as protein markers in cancer. Quantitative proteomic profiling of circulating microvesicles and exosomes can be a high-throughput platform for discovery of novel molecular insights and putative markers. Hence, this study aimed to investigate proteome dynamics of plasma-derived microvesicles an  ...[more]

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