TY - JOUR
T1 - Serological immune response against ADAM10 pro-domain is associated with favourable prognosis in stage III colorectal cancer patients
AU - Álvarez-Fernández, Sheila María
AU - Barbariga, Marco
AU - Cannizzaro, Luca
AU - Cannistraci, Carlo Vittorio
AU - Hurley, Laura
AU - Zanardi, Alan
AU - Conti, Antonio
AU - Sanvito, Francesca
AU - Innocenzi, Anna
AU - Pecorelli, Nicolò
AU - Braga, Marco
AU - Alessio, Massimo
PY - 2016
Y1 - 2016
N2 - A humoral immune response against aberrant tumor proteins can be elicited in cancer patients, resulting in the production of auto-antibodies (Abs). By serological proteome analysis we identified the surface membrane protein ADAM10, a metalloproteinase that has a role in epithelial-tumor progression and invasion, as a target of the immune response in colorectal cancer (Crc). A screening carried out on the purified protein using testing cohorts of sera (Crc patients n = 57; control subjects n = 39) and validation cohorts of sera (Crc patients n = 49; control subjects n = 52) indicated that anti-ADAM10 auto-Abs were significantly induced in a large group (74%) of colon cancer patients, in particular in patients at stage II and III of the disease. Interestingly, in Crc patients classified as stage III disease, the presence of anti-ADAM10 auto-Abs in the sera was associated with a favourable follow-up with a significant shifting of the recurrence-free survival median time from 23 to 55 months. Even though the ADAM10 protein was expressed in Crc regardless the presence of auto-Abs, the immature/non-functional isoform of ADAM10 was highly expressed in the tumor of anti-ADAM10-positive patients and was the isoform targeted by the auto-Abs. In conclusion, the presence of anti-ADAM10 auto-Abs seems to reflect the increased tumor expression of the immunogenic immature-ADAM10 in a group of Crc patients, and is associated with a favourable prognosis in patients at stage III of the disease.
AB - A humoral immune response against aberrant tumor proteins can be elicited in cancer patients, resulting in the production of auto-antibodies (Abs). By serological proteome analysis we identified the surface membrane protein ADAM10, a metalloproteinase that has a role in epithelial-tumor progression and invasion, as a target of the immune response in colorectal cancer (Crc). A screening carried out on the purified protein using testing cohorts of sera (Crc patients n = 57; control subjects n = 39) and validation cohorts of sera (Crc patients n = 49; control subjects n = 52) indicated that anti-ADAM10 auto-Abs were significantly induced in a large group (74%) of colon cancer patients, in particular in patients at stage II and III of the disease. Interestingly, in Crc patients classified as stage III disease, the presence of anti-ADAM10 auto-Abs in the sera was associated with a favourable follow-up with a significant shifting of the recurrence-free survival median time from 23 to 55 months. Even though the ADAM10 protein was expressed in Crc regardless the presence of auto-Abs, the immature/non-functional isoform of ADAM10 was highly expressed in the tumor of anti-ADAM10-positive patients and was the isoform targeted by the auto-Abs. In conclusion, the presence of anti-ADAM10 auto-Abs seems to reflect the increased tumor expression of the immunogenic immature-ADAM10 in a group of Crc patients, and is associated with a favourable prognosis in patients at stage III of the disease.
KW - ADAM10 metalloprotease
KW - Autoantibodies
KW - Colorectal carcinoma
KW - Immuno-proteomics
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=84999040240&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.11181
DO - 10.18632/oncotarget.11181
M3 - Article
C2 - 27517630
AN - SCOPUS:84999040240
SN - 1949-2553
VL - 7
SP - 80059
EP - 80076
JO - Oncotarget
JF - Oncotarget
IS - 48
ER -