Cancer therapy
A cancer and mycobacterial technology, applied in antibody medical ingredients, bacterial medical raw materials, drug combinations, etc., can solve the problems of worsening inflammatory response and side effects
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[0107] This example describes the study of heat-killed, whole-cell Mycobacterium albicans (IMM-101) and the mTor inhibitor rapamycin (West. Romos). Genetically engineered mice carrying mutations in Kras and Pdx-Cre (KC mice) were bred according to the method described by Hingorani et al. (Cancer Cell, 2003, 4:437-50); Ductal lesions of intraepithelial neoplasia that can progress to invasive and metastatic adenocarcinoma. Using 10 mutants in Kras, p53 and Pdx-Cre 5 KC mice were orthotopically injected with KPC cells (Hingorani et al., Cancer Cell, 2005, 7:469-48) at postnatal day 100. On day 114 ( figure 1 Day 0 in ) mice were treated as follows:
[0108] - 12 mice were untreated (control);
[0109] - 12 mice were treated with 2 mg / kg rapamycin intraperitoneally daily for the entire length of the study;
[0110]- 12 mice were treated with 0.1 mg IMM-101 / mouse, alternately injected subcutaneously in the nape of the neck and at the base of the tail on alternate days during ...
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