TY - JOUR
T1 - Establishment of an antibody specific for cancer-associated haptoglobin
T2 - A possible implication of clinical investigation
AU - Nishino, Kimihiro
AU - Koda, Sayaka
AU - Kataoka, Naoya
AU - Takamatsu, Shinji
AU - Nakano, Miyako
AU - Ikeda, Shun
AU - Kamamatsu, Yuka
AU - Morishita, Koichi
AU - Moriwaki, Kenta
AU - Eguchi, Hidetoshi
AU - Yamamoto, Eiko
AU - Kikkawa, Fumitaka
AU - Tomita, Yasuhiko
AU - Kamada, Yoshihiro
AU - Miyoshi, Eiji
N1 - Publisher Copyright:
© Nishino et al.
PY - 2018
Y1 - 2018
N2 - We previously found that the serum level of fucosylated haptoglobin (Fuc- Hpt) was significantly increased in pancreatic cancer patients. To delineate the mechanism underlying this increase and develop a simple detection method, we set out to generate a monoclonal antibody (mAb) specific for Fuc-Hpt. After multiple screenings by enzyme-linked immunosorbent assay (ELISA), a 10-7G mAb was identified as being highly specific for Fuc-Hpt generated in a cell line as well as for Hpt derived from a pancreatic cancer patient. As a result from affinity chromatography with 10-7G mAb, followed by lectin blot and mass spectrometry analyses, it was found that 10-7G mAb predominantly recognized both Fuc-Hpt and prohaptoglobin (proHpt), which was also fucosylated. In immunohistochemical analyses, hepatocytes surrounding metastasized cancer cells were stained by the 10-7G mAb, but neither the original cancer cells themselves nor normal hepatocytes exhibited positive staining, suggesting that metastasized cancer cells promote Fuc-Hpt production in adjacent hepatocytes. Serum level of Fuc-Hpt determined with newly developed ELISA system using the 10-7G mAb, was increased in patients of pancreatic and colorectal cancer. Interestingly, dramatic increases in Fuc-Hpt levels were observed at the stage IV of colorectal cancer. These results indicate that the 10-7G mAb developed is a promising antibody which recognizes Fuc-Hpt and could be a useful diagnostic tool for detecting liver metastasis of cancer.
AB - We previously found that the serum level of fucosylated haptoglobin (Fuc- Hpt) was significantly increased in pancreatic cancer patients. To delineate the mechanism underlying this increase and develop a simple detection method, we set out to generate a monoclonal antibody (mAb) specific for Fuc-Hpt. After multiple screenings by enzyme-linked immunosorbent assay (ELISA), a 10-7G mAb was identified as being highly specific for Fuc-Hpt generated in a cell line as well as for Hpt derived from a pancreatic cancer patient. As a result from affinity chromatography with 10-7G mAb, followed by lectin blot and mass spectrometry analyses, it was found that 10-7G mAb predominantly recognized both Fuc-Hpt and prohaptoglobin (proHpt), which was also fucosylated. In immunohistochemical analyses, hepatocytes surrounding metastasized cancer cells were stained by the 10-7G mAb, but neither the original cancer cells themselves nor normal hepatocytes exhibited positive staining, suggesting that metastasized cancer cells promote Fuc-Hpt production in adjacent hepatocytes. Serum level of Fuc-Hpt determined with newly developed ELISA system using the 10-7G mAb, was increased in patients of pancreatic and colorectal cancer. Interestingly, dramatic increases in Fuc-Hpt levels were observed at the stage IV of colorectal cancer. These results indicate that the 10-7G mAb developed is a promising antibody which recognizes Fuc-Hpt and could be a useful diagnostic tool for detecting liver metastasis of cancer.
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U2 - 10.18632/oncotarget.24332
DO - 10.18632/oncotarget.24332
M3 - Article
AN - SCOPUS:85042560216
SN - 1949-2553
VL - 9
SP - 12732
EP - 12744
JO - Oncotarget
JF - Oncotarget
IS - 16
ER -