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用于原发性人类乳腺肿瘤克隆生长的改良培养条件。

Improved culture conditions for clonogenic growth of primary human breast tumours.

作者信息

Hug V, Haynes M, Rashid R, Spitzer G, Blumenschen G, Hortobagyi G

出版信息

Br J Cancer. 1984 Aug;50(2):207-13. doi: 10.1038/bjc.1984.164.

Abstract

Four established human breast tumour cell lines with different biologic properties were selected for study and requirements for their clonogenic growth in semisolid cultures were identified. The conventional conditions were modified by factors that enhanced colony formation of 3 or more of these cell lines. The modified culture conditions were then applied to the growth in agar of primary breast tumours. A 5-fold improvement in plating efficiency was observed when cultures of 105 primary tumours grown under these modified conditions were compared to those of 52 tumours grown earlier under conventional conditions, and a 4-fold improvement resulted from the addition of hormones and conditioned medidum in 26 tumours cultured simultaneously under both conditions. The biologic relevance of these clonogens recovered in vitro was substantiated by a 70% concordance of in vitro and in vivo tumour sensitivity to anticancer drugs.

摘要

选择了四种具有不同生物学特性的成熟人乳腺肿瘤细胞系进行研究,并确定了它们在半固体培养中克隆生长的条件。通过能增强其中3种或更多种细胞系集落形成的因素对常规条件进行了改良。然后将改良后的培养条件应用于原发性乳腺肿瘤在琼脂中的生长。当将在这些改良条件下培养的105个原发性肿瘤的培养物与早期在常规条件下培养的52个肿瘤的培养物进行比较时,观察到接种效率提高了5倍,并且在两种条件下同时培养的26个肿瘤中添加激素和条件培养基后,接种效率提高了4倍。体外回收的这些克隆原的生物学相关性通过体外和体内肿瘤对抗癌药物敏感性的70%一致性得到证实。

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引用本文的文献

本文引用的文献

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Human tumor cloning: feasibility and clinical correlations.人类肿瘤克隆:可行性及临床关联
Cancer Chemother Pharmacol. 1981;6(3):265-71. doi: 10.1007/BF00256979.
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Human tumor clonogenic assays. An overview.
Cancer Chemother Pharmacol. 1981;6(3):201-3. doi: 10.1007/BF00256971.
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The growth of mouse bone marrow cells in vitro.小鼠骨髓细胞的体外生长
Aust J Exp Biol Med Sci. 1966 Jun;44(3):287-99. doi: 10.1038/icb.1966.28.
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Primary bioassay of human tumor stem cells.人类肿瘤干细胞的初步生物测定。
Science. 1977 Jul 29;197(4302):461-3. doi: 10.1126/science.560061.
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Primary bioassay of human myeloma stem cells.人骨髓瘤干细胞的原代生物测定
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