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Alterations of the Plasma Peptidome Profiling in Colorectal Cancer Progression
Journal of cellular physiology, 2016-04, Vol.231 (4), p.915-925
Bedin, Chiara
Crotti, Sara
Ragazzi, Eugenio
Pucciarelli, Salvatore
Agatea, Lisa
Tasciotti, Ennio
Ferrari, Mauro
Traldi, Pietro
Rizzolio, Flavio
Giordano, Antonio
Nitti, Donato
Agostini, Marco
2016
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Bedin, Chiara
Crotti, Sara
Ragazzi, Eugenio
Pucciarelli, Salvatore
Agatea, Lisa
Tasciotti, Ennio
Ferrari, Mauro
Traldi, Pietro
Rizzolio, Flavio
Giordano, Antonio
Nitti, Donato
Agostini, Marco
Titel
Alterations of the Plasma Peptidome Profiling in Colorectal Cancer Progression
Ist Teil von
Journal of cellular physiology, 2016-04, Vol.231 (4), p.915-925
Ort / Verlag
United States: Blackwell Publishing Ltd
Erscheinungsjahr
2016
Quelle
Wiley Online Library Journals【Remote access available】
Beschreibungen/Notizen
Early detection of colorectal cancer (CRC) remains a challenge. It has been highlighted that the pathological alterations within an organ and tissues might be reflected in serum or plasma proteomic/peptidic patterns. The aim of the study was to follow the changes in the plasma peptides associated to colorectal cancer progression by mass spectrometry. This study included 27 adenoma, 67 CRC (n = 33 I–II stage and n = 34 III–IV stage), 23 liver metastasis from CRC patients and 34 subjects disease‐free as controls. For plasma peptides analysis, samples purification was performed on the Nanoporous Silica Chips technology followed by matrix‐assisted laser desorption/ionisation‐time of flight analysis. Since the high complexity of the obtained dataset, multivariate statistical analysis, and discriminant pattern recognition were performed for study groups classification. Forty‐four of 88 ionic species were successfully identified as fragments of peptides and proteins physiologically circulating in the blood and belonging to immune and coagulation systems and inflammatory mediators. Many peptides clustered into sets of overlapping sequences with ladder‐like truncation clearly associated to proteolytic processes of both endo‐ and exoproteases activity. Comparing to controls, a different median ion intensity of the group‐type fragments distribution was observed. Moreover, the degradation pattern obtained by proteolytic cleavage was different into study groups. This pattern was specific and characteristic of each group: controls, colon tumour disease (including adenoma and CRC), and liver metastasis, revealing a role as biomarker in early diagnosis and prognosis. Our findings highlighted peculiar changes in protease activity characteristic of CRC progression from pre‐cancer lesion to metastatic disease. J. Cell. Physiol. 231: 915–925, 2016. © 2015 Wiley Periodicals, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 0021-9541
eISSN: 1097-4652
DOI: 10.1002/jcp.25196
Titel-ID: cdi_proquest_miscellaneous_1802744253
Format
–
Schlagworte
Adult
,
Aged
,
Aged, 80 and over
,
Amino Acid Sequence
,
Analysis of Variance
,
Colorectal carcinoma
,
Colorectal Neoplasms - blood
,
Colorectal Neoplasms - pathology
,
Disease Progression
,
Female
,
Humans
,
Male
,
Mass spectrometry
,
Middle Aged
,
Pattern recognition
,
Peptide Hydrolases - metabolism
,
Peptides
,
Peptides - blood
,
Peptides - chemistry
,
Silica
,
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
,
Statistical analysis
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