CD22 Antigen Is Broadly Expressed on Lung Cancer Cells and Is a Target for Antibody-Based Therapy

被引:27
作者
Tuscano, Joseph M. [1 ,2 ]
Kato, Jason [1 ]
Pearson, David [3 ]
Xiong, Chengyi [1 ]
Newell, Laura [4 ]
Ma, Yunpeng [1 ]
Gandara, David R. [1 ]
O'Donnell, Robert T. [1 ,2 ]
机构
[1] Univ Calif Davis, Ctr Comprehens Canc, Dept Internal Med, Div Hematol & Oncol, Sacramento, CA 95817 USA
[2] No Calif Healthcare Syst, Dept Vet Affairs, Mather, CA USA
[3] Calif Northstate Univ, Coll Pharm, Rancho Cordova, CA USA
[4] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
关键词
B-LYMPHOCYTE SURVIVAL; NON-HODGKINS-LYMPHOMA; SIGNAL-TRANSDUCTION; ANTITUMOR-ACTIVITY; RECEPTOR; LIGAND; ADHESION; BINDING; IDENTIFICATION; ENDOCYTOSIS;
D O I
10.1158/0008-5472.CAN-12-0173
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. Cancer Res; 72(21); 5556-65. (C)2012 AACR.
引用
收藏
页码:5556 / 5565
页数:10
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