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本文引用的文献

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DYNAMICS OF TUMOUR GROWTH: COMPARISON OF GROWTH RATES AND EXTRAPOLATION OF GROWTH CURVE TO ONE CELL.肿瘤生长动力学:生长速率比较及生长曲线外推至单个细胞
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Changes in the proliferation characteristics of a solid transplantable tumour of the mouse with time after transplantation.
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Evidence for discrete cell kinetic subpopulations in mouse epidermis based on mathematical analysis.基于数学分析的小鼠表皮离散细胞动力学亚群的证据。
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Proliferation kinetics of a human malignant melanoma serially grown in nude mice.在裸鼠体内连续传代培养的人恶性黑色素瘤的增殖动力学
Cell Tissue Kinet. 1984 Jul;17(4):401-10. doi: 10.1111/j.1365-2184.1984.tb00599.x.
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Kinetics of cell proliferation of an experimental tumor.实验性肿瘤的细胞增殖动力学
Cancer Res. 1967 Jun;27(6):1122-31.
6
A comparison of cell proliferation parameters in solid and ascites Ehrlich tumors.实体型和腹水型艾氏瘤细胞增殖参数的比较。
Cancer Res. 1969 Aug;29(8):1527-34.
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Changes of cell proliferation characteristics in a rat rhabdomyosarcoma before and after x-irradiation.
Eur J Cancer (1965). 1969 May;5(2):173-89. doi: 10.1016/0014-2964(69)90065-6.
8
Kinetics of proliferation, migration, and death of L1210 ascites cells.L1210腹水癌细胞的增殖、迁移和死亡动力学
Cancer Res. 1971 Apr;31(4):402-8.
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Kinetic parameters and growth curves for experimental tumor systems.
Cancer Chemother Rep. 1970 Jun;54(3):143-74.
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Age-specific changes in the proliferation of Ehrlich ascites tumor cells grown as solid tumors.作为实体瘤生长的艾氏腹水瘤细胞增殖的年龄特异性变化。
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裸鼠体内生长的人恶性黑色素瘤的生长依赖性细胞增殖动力学

Growth dependent cell proliferation kinetics of a human malignant melanoma grown in nude mice.

作者信息

Wickramanayake P D, Loeffler M, Klein H O, Groth W, Wichmann H E

出版信息

J Cancer Res Clin Oncol. 1985;110(1):11-6. doi: 10.1007/BF00402496.

DOI:10.1007/BF00402496
PMID:4019566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12253287/
Abstract

A human malignant melanoma was grown in nude mice. The tumour showed an exponential growth for several weeks which gradually slowed down, until following week 8 the tumour growth ceased. The reasons for this growth pattern were examined by labelling techniques (PLM, LI). The tumour cell production as quantified by the growth fraction, showed only a moderate reduction which, taken alone, could not explain the growth cessation. The important mechanism seems to be an increased loss of tumour cells during the intermitotic interval. While the loss of cells/h remains constant the total intermitotic cell loss is increased because the cell cycle times are prolonged by 50% from the exponential phase (45 h in week 3) to the plateau phase (66 h in week 8).

摘要

将人类恶性黑色素瘤接种于裸鼠体内。肿瘤在数周内呈指数生长,随后逐渐减缓,直至第8周后肿瘤生长停止。通过标记技术(PLM、LI)研究了这种生长模式的原因。通过生长分数量化的肿瘤细胞产生仅出现适度降低,仅据此无法解释生长停止现象。重要的机制似乎是在分裂间期肿瘤细胞损失增加。虽然每小时的细胞损失保持恒定,但总的分裂间期细胞损失增加,因为细胞周期时间从指数生长期(第3周为45小时)到平台期(第8周为66小时)延长了50%。