Proteomics

Dataset Information

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Detection of Five Solid Carcinomas Using Blood Circulating Proteins


ABSTRACT: When diagnosed in a metastatic stage cancer is mostly incurable making its early detection via biomarkers of immense clinical interest. Proteins circulating in blood are a preferred source of biomarkers for a wide range of cancers due to the ease and non-invasiveness of collection. Our approach to cancer biomarker discovery is based on the observation that proteomic changes in tumor tissue are remotely detectable as changes in the protein composition of blood plasma. To determine whether these changes in the plasma of patients are specific for their specific cancer or represent a response to cancer in general we performed a cross-tumor plasma proteomic study. Using a proteomic serum/plasma workflow consisting of the combined use of N-glycosite enrichment and SWATH mass spectrometry (SWATH-MS), we investigated 155 blood samples derived from cohorts of patients with carcinomas at a localized or locally advanced clinical stage, or from a matched control group. A quantitative comparison of the resulting N-glycosite profiles indicated that some biomarkers are common to several cancers, while others are highly specific for one cancer type.

INSTRUMENT(S): TripleTOF 5600

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Plasma, Blood Serum

DISEASE(S): Lung Cancer,Prostate Adenocarcinoma,Colon Cancer,Pancreatic Cancer,Malignant Neoplasm Of Ovary

SUBMITTER: Tatjana Sajic  

LAB HEAD: Ruedi Aebersold

PROVIDER: PXD004998 | Pride | 2018-08-09

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
CrossTumourStudy_sample_annotataion.txt Txt
DDA_files.txt Txt
LibrarySWATH_Nglyco_plasma.TraML Other
Panc_sample_annotataion_ValidationExp_2017.txt Txt
Proc_sample_annotataion_ValidExp_2017.txt Txt
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Publications


Cancer is mostly incurable when diagnosed at a metastatic stage, making its early detection via blood proteins of immense clinical interest. Proteomic changes in tumor tissue may lead to changes detectable in the protein composition of circulating blood plasma. Using a proteomic workflow combining N-glycosite enrichment and SWATH mass spectrometry, we generate a data resource of 284 blood samples derived from patients with different types of localized-stage carcinomas and from matched controls.  ...[more]

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