Kanwar J R, Shen W P, Kanwar R K, Berg R W, Krissansen G W
Division of Molecular Medicine, Faculty of Medicine and Health Science, University of Auckland, New Zealand.
J Natl Cancer Inst. 2001 Oct 17;93(20):1541-52. doi: 10.1093/jnci/93.20.1541.
Survivin, a member of the inhibitor of apoptosis (IAP) protein family, is detectable in most types of cancer, and its presence is associated with a poor prognosis. We determined the effects of gene-based therapies that inhibit survivin function in a mouse tumor model.
Using five to six mice per treatment group, we injected tumors derived from mouse EL-4 thymic lymphoma cells with plasmids encoding antisense survivin, a dominant-negative mutant survivin, and the T-cell costimulator B7-1. Expression of endogenous survivin and the proteins encoded by the injected plasmids were examined by immunohistochemical staining of tumor sections and by western blot and flow cytometry analyses of isolated tumor cells. Tumor growth, the generation of antitumor cytotoxic T-lymphocyte (CTL) activity, apoptosis, and the contribution of leukocyte subsets to antitumor activity were measured. All statistical tests were two-sided.
Large (1.0-cm diameter) tumors had approximately 10-fold more survivin than small (0.2-cm diameter) tumors. At 28 days after injection, antisense and dominant-negative mutant survivin plasmids statistically significantly inhibited the growth of both small (P =.006 and P =.0018, respectively) and large (P<.001 for both plasmids) EL-4 tumors compared with tumors injected with empty plasmid. The growth of large tumors was further inhibited by intratumoral injection with antisense survivin and B7-1 (P =.004); thus, inhibition of survivin expression renders large tumors susceptible to B7-1-mediated immunotherapy. Mice whose tumors were completely eradicated by injection of B7-1 remained tumor free for 26 days after re-injection with EL-4 cells (when the experiment ended). Compared with tumors injected with empty plasmid, tumors injected with survivin-based plasmids had increased apoptosis, and animals bearing such tumors generated more antitumor CTLs.
Intratumoral injection of plasmids that block survivin expression and stimulate the generation of tumor-specific CTLs may be beneficial for the treatment of large lymphomas.
生存素是凋亡抑制蛋白(IAP)家族的成员之一,在大多数癌症类型中均可检测到,其存在与预后不良相关。我们在小鼠肿瘤模型中确定了抑制生存素功能的基因疗法的效果。
每个治疗组使用5至6只小鼠,我们将编码反义生存素、显性负性突变体生存素和T细胞共刺激分子B7-1的质粒注射到源自小鼠EL-4胸腺淋巴瘤细胞的肿瘤中。通过肿瘤切片的免疫组织化学染色以及分离的肿瘤细胞的蛋白质印迹和流式细胞术分析来检测内源性生存素和注射质粒所编码蛋白质的表达。测量肿瘤生长、抗肿瘤细胞毒性T淋巴细胞(CTL)活性的产生、细胞凋亡以及白细胞亚群对抗肿瘤活性的贡献。所有统计检验均为双侧检验。
大的(直径1.0厘米)肿瘤的生存素含量比小的(直径0.2厘米)肿瘤多大约10倍。注射后28天,与注射空质粒的肿瘤相比,反义生存素和显性负性突变体生存素质粒在统计学上显著抑制了小的(分别为P = 0.006和P = 0.0018)和大的(两种质粒的P均<0.001)EL-4肿瘤的生长。大肿瘤的生长通过瘤内注射反义生存素和B7-1进一步受到抑制(P = 0.004);因此,抑制生存素表达使大肿瘤对B7-1介导的免疫疗法敏感。其肿瘤通过注射B7-1被完全根除的小鼠在重新注射EL-4细胞后(实验结束时)26天内无肿瘤复发。与注射空质粒的肿瘤相比,注射基于生存素的质粒的肿瘤细胞凋亡增加,并且携带此类肿瘤的动物产生了更多的抗肿瘤CTL。
瘤内注射阻断生存素表达并刺激肿瘤特异性CTL产生的质粒可能对大淋巴瘤的治疗有益。