Name | Trabedersen |
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Description | Trabedersen (AP 12009) is an antisense oligodeoxynucleotide that specifically inhibits TGF-β2 (TGF-beta/Smad). Trabedersen can be used for the study of malignant brain tumors and other solid tumors overexpressing TGF-β2, such as those of the skin, pancreas and colon[1][2]. |
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Related Catalog | |
In Vitro | Trabedersen (1-80 μM; 7 days) 减少人胰腺癌细胞系 Hup-T3 中 TGF-β2 的分泌,IC50 在低 μM 范围内,明显抑制细胞增殖,并完全阻断迁移 胰腺癌细胞[2]。 Trabedersen 逆转 TGF-β2 介导的胰腺癌细胞免疫抑制[2]。 Cell Proliferation Assay[2] Cell Line: Hup-T3 cells Concentration: 1 μM, 2.5 μM, 5 μM, 10 μM, 20 μM, 40 μM, 60 μM, 80 μM Incubation Time: 7 days Result: Inhibited cell proliferation, and completely blocked migration of pancreatic cancer cells. |
In Vivo | Trabedersen(初始负荷剂量为 50 mg/kg ,随后每周 3 次 16 mg/kg;i.p.)可显著降低转移性胰腺癌原位小鼠模型中的肿瘤生长、淋巴结转移和血管生成[2]。 Animal Model: Eight-week-old male athymic nude mice (BALB⁄Cnu ⁄nu) bearing human pancreatic cancer cells[2]. Dosage: Initial loading dose of 50 mg/kg bodyweight followed by 16 mg/kg three times a week. Administration: Intraperitoneal (i.p.) injection; three times a week; for 27 days Result: Significantly reduced tumor growth, lymph node metastasis and angiogenesis. |
References |
Molecular Weight | 5770.75 |
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