TY - JOUR
T1 - CD22 antigen is broadly expressed on lung cancer cells and is a target for antibody-based therapy
AU - Tuscano, Joseph M.
AU - Kato, Jason
AU - Pearson, David
AU - Xiong, Chengyi
AU - Newell, Laura
AU - Ma, Yunpeng
AU - Gandara, David R.
AU - O'Donnell, Robert T.
PY - 2012/11/1
Y1 - 2012/11/1
N2 - Most patients with lung cancer still die from their disease, necessitating additional options to improve treatment. Here, we provide evidence for targeting CD22, a cell adhesion protein known to influence B-cell survival that we found is also widely expressed in lung cancer cells. In characterizing the antitumor activity of an established anti-CD22 monoclonal antibody (mAb), HB22.7, we showed CD22 expression by multiple approaches in various lung cancer subtypes, including 7 of 8 cell lines and a panel of primary patient specimens. HB22.7 displayed in vitro and in vivo cytotoxicity against CD22-positive human lung cancer cells and tumor xenografts. In a model of metastatic lung cancer, HB22.7 inhibited the development of pulmonary metastasis and extended overall survival. The finding that CD22 is expressed on lung cancer cells is significant in revealing a heretofore unknown mechanism of tumorigenesis and metastasis. Our work suggests that anti- CD22 mAbs may be useful for targeted therapy of lung cancer, a malignancy that has few tumor-specific targets.
AB - Most patients with lung cancer still die from their disease, necessitating additional options to improve treatment. Here, we provide evidence for targeting CD22, a cell adhesion protein known to influence B-cell survival that we found is also widely expressed in lung cancer cells. In characterizing the antitumor activity of an established anti-CD22 monoclonal antibody (mAb), HB22.7, we showed CD22 expression by multiple approaches in various lung cancer subtypes, including 7 of 8 cell lines and a panel of primary patient specimens. HB22.7 displayed in vitro and in vivo cytotoxicity against CD22-positive human lung cancer cells and tumor xenografts. In a model of metastatic lung cancer, HB22.7 inhibited the development of pulmonary metastasis and extended overall survival. The finding that CD22 is expressed on lung cancer cells is significant in revealing a heretofore unknown mechanism of tumorigenesis and metastasis. Our work suggests that anti- CD22 mAbs may be useful for targeted therapy of lung cancer, a malignancy that has few tumor-specific targets.
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U2 - 10.1158/0008-5472.CAN-12-0173
DO - 10.1158/0008-5472.CAN-12-0173
M3 - Article
C2 - 22986740
AN - SCOPUS:84868262326
SN - 0008-5472
VL - 72
SP - 5556
EP - 5565
JO - Cancer Research
JF - Cancer Research
IS - 21
ER -