SK-BR-3
特徵
SK-BR-3細胞與AU565細胞分離自同一名曾接受過放射及5-氟尿嘧啶等治療的患者[2]。SK-BR-3細胞源自於一名43歲白人女性患者體內,由乳癌引起的胸腔積液[1],並且過度表達着HER2/neu產物,而該產物被認為與多種乳癌增殖的途徑有關。SK-BR-3細胞已知會以葡萄狀簇 (grape-like clusters)的形式生長,其侵襲性表型與體內細胞類似[3]。
科研用途
SK-BR-3細胞已用於尋求能克服曲妥珠單抗對乳腺癌 (過度表達人類表皮生長因子受體2)的抵抗力的研究[4]。而且有科研人員已經檢查了該細胞系在CRISPR/Cas9基因編輯與轉染中的抗體抗性[5],以及在微環境存在波動的情況下,基於HER2/neu的癌症治療中的應用[6]。
參考資料
- . Memorial Sloan-Kettering Cancer Center. [2018-06-18]. (原始内容存档于2018-06-18).
- . Addex Bio. [2018-06-18]. (原始内容存档于2018-06-19).
- Holliday, DL; Speirs, V. . Breast cancer research : BCR. 2011-08-12, 13 (4): 215 [2020-01-05]. PMID 21884641. doi:10.1186/bcr2889.
- Tseng, PH; Wang, YC; Weng, SC; Weng, JR; Chen, CS; Brueggemeier, RW; Shapiro, CL; Chen, CY; Dunn, SE; Pollak, M; Chen, CS. . Molecular pharmacology. 2006-11, 70 (5): 1534–41 [2020-01-05]. PMID 16887935. doi:10.1124/mol.106.023911.
- Cao, J; Wu, L; Zhang, SM; Lu, M; Cheung, WK; Cai, W; Gale, M; Xu, Q; Yan, Q. . Nucleic acids research. 2016-11-02, 44 (19): e149 [2020-01-05]. PMID 27458201. doi:10.1093/nar/gkw660.
- Weigelt, B; Lo, AT; Park, CC; Gray, JW; Bissell, MJ. . Breast cancer research and treatment. 2010-07, 122 (1): 35–43 [2020-01-05]. PMID 19701706. doi:10.1007/s10549-009-0502-2.
外部連結
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