SILAC‐based quantitative proteomic analysis of gastric cancer secretome. Issue 5 (21st May 2013)
- Record Type:
- Journal Article
- Title:
- SILAC‐based quantitative proteomic analysis of gastric cancer secretome. Issue 5 (21st May 2013)
- Main Title:
- SILAC‐based quantitative proteomic analysis of gastric cancer secretome
- Authors:
- Marimuthu, Arivusudar
Subbannayya, Yashwanth
Sahasrabuddhe, Nandini A.
Balakrishnan, Lavanya
Syed, Nazia
Sekhar, Nirujogi Raja
Katte, Teesta V.
Pinto, Sneha M.
Srikanth, Srinivas M.
Kumar, Praveen
Pawar, Harsh
Kashyap, Manoj K.
Maharudraiah, Jagadeesha
Ashktorab, Hassan
Smoot, Duane T.
Ramaswamy, Girija
Kumar, Rekha V.
Cheng, Yulan
Meltzer, Stephen J.
Roa, Juan Carlos
Chaerkady, Raghothama
Prasad, T. S. Keshava
Harsha, H. C.
Chatterjee, Aditi
Pandey, Akhilesh
Semmes, O. John
Conrads, Thomas P. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="prca1441-sec-0010" sec-type="section"> <title>Purpose</title> <p>Gastric cancer is a commonly occurring cancer in Asia and one of the leading causes of cancer deaths. However, there is no reliable blood‐based screening test for this cancer. Identifying proteins secreted from tumor cells could lead to the discovery of clinically useful biomarkers for early detection of gastric cancer.</p> </sec> <sec id="prca1441-sec-0020" sec-type="section"> <title>Experimental design</title> <p>A SILAC‐based quantitative proteomic approach was employed to identify secreted proteins that were differentially expressed between neoplastic and non‐neoplastic gastric epithelial cells. Proteins from the secretome were subjected to SDS‐PAGE and SCX‐based fractionation, followed by mass spectrometric analysis on an LTQ‐Orbitrap Velos mass spectrometer. Immunohistochemical labeling was employed to validate a subset of candidates using tissue microarrays.</p> </sec> <sec id="prca1441-sec-0030" sec-type="section"> <title>Results</title> <p>We identified 2205 proteins in the gastric cancer secretome of which 263 proteins were overexpressed greater than fourfold in gastric cancer‐derived cell lines as compared to non‐neoplastic gastric epithelial cells. Three candidate proteins, proprotein convertase subtilisin/kexin type 9 (<italic>PCSK9</italic>), lectin mannose binding 2 (<italic>LMAN2</italic>), and<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="prca1441-sec-0010" sec-type="section"> <title>Purpose</title> <p>Gastric cancer is a commonly occurring cancer in Asia and one of the leading causes of cancer deaths. However, there is no reliable blood‐based screening test for this cancer. Identifying proteins secreted from tumor cells could lead to the discovery of clinically useful biomarkers for early detection of gastric cancer.</p> </sec> <sec id="prca1441-sec-0020" sec-type="section"> <title>Experimental design</title> <p>A SILAC‐based quantitative proteomic approach was employed to identify secreted proteins that were differentially expressed between neoplastic and non‐neoplastic gastric epithelial cells. Proteins from the secretome were subjected to SDS‐PAGE and SCX‐based fractionation, followed by mass spectrometric analysis on an LTQ‐Orbitrap Velos mass spectrometer. Immunohistochemical labeling was employed to validate a subset of candidates using tissue microarrays.</p> </sec> <sec id="prca1441-sec-0030" sec-type="section"> <title>Results</title> <p>We identified 2205 proteins in the gastric cancer secretome of which 263 proteins were overexpressed greater than fourfold in gastric cancer‐derived cell lines as compared to non‐neoplastic gastric epithelial cells. Three candidate proteins, proprotein convertase subtilisin/kexin type 9 (<italic>PCSK9</italic>), lectin mannose binding 2 (<italic>LMAN2</italic>), and PDGFA‐associated protein 1 (<italic>PDAP1</italic>) were validated by immunohistochemical labeling.</p> </sec> <sec id="prca1441-sec-0040" sec-type="section"> <title>Conclusions and clinical relevance</title> <p>We report here the largest cancer secretome described to date. The novel biomarkers identified in the current study are excellent candidates for further testing as early detection biomarkers for gastric adenocarcinoma.</p> </sec> </abstract> … (more)
- Is Part Of:
- Proteomics. Volume 7:Issue 5/6(2013)
- Journal:
- Proteomics
- Issue:
- Volume 7:Issue 5/6(2013)
- Issue Display:
- Volume 7, Issue 5/6 (2013)
- Year:
- 2013
- Volume:
- 7
- Issue:
- 5/6
- Issue Sort Value:
- 2013-0007-NaN-0000
- Page Start:
- 355
- Page End:
- 366
- Publication Date:
- 2013-05-21
- Subjects:
- Proteomics -- Periodicals
572.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1862-8354 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/prca.201200069 ↗
- Languages:
- English
- ISSNs:
- 1862-8346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.178500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3115.xml