TY - JOUR
T1 - Novel Proteome Extraction Method Illustrates a Conserved Immunological Signature of MSI-H Colorectal Tumors
AU - Vainer, Elez D.
AU - Kania-Almog, Juliane
AU - Zatara, Ghadeer
AU - Levin, Yishai
AU - Vainer, Gilad W.
N1 - Publisher Copyright:
© 2020 Vainer et al.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Using a simple, environment friendly proteome extraction (TOP), we were able to optimize the analysis of clinical samples. Using our TOP method we analyzed a clinical cohort of microsatellite stable (MSS) and unstable (MSI-H) colorectal carcinoma (CRC). We identified a tumor cell specific, STAT1-centered, immune signature expressed by the MSI-H tumor cells. We then showed that long, but not short, exposure to Interferon-g induces a similar signature in vitro. We identified 10 different temporal protein expression patterns, classifying the Interferon-g protein temporal regulation in CRC. Our data sheds light on the changes that tumor cells undergo under long-term immunological pressure in vivo, the importance of STAT proteins in specific biological scenarios. The data generated could help find novel clinical biomarkers and therapeutic approaches.
AB - Using a simple, environment friendly proteome extraction (TOP), we were able to optimize the analysis of clinical samples. Using our TOP method we analyzed a clinical cohort of microsatellite stable (MSS) and unstable (MSI-H) colorectal carcinoma (CRC). We identified a tumor cell specific, STAT1-centered, immune signature expressed by the MSI-H tumor cells. We then showed that long, but not short, exposure to Interferon-g induces a similar signature in vitro. We identified 10 different temporal protein expression patterns, classifying the Interferon-g protein temporal regulation in CRC. Our data sheds light on the changes that tumor cells undergo under long-term immunological pressure in vivo, the importance of STAT proteins in specific biological scenarios. The data generated could help find novel clinical biomarkers and therapeutic approaches.
UR - http://www.scopus.com/inward/record.url?scp=85092680526&partnerID=8YFLogxK
U2 - 10.1074/mcp.RA120.002152
DO - 10.1074/mcp.RA120.002152
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C2 - 32641473
AN - SCOPUS:85092680526
SN - 1535-9476
VL - 19
SP - 1619
EP - 1631
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 10
ER -