Interleukin 6 decreases cell-cell association and increases motility of ductal breast carcinoma cells.
Interleukin 6 decreases cell-cell association and increases motility of ductal breast carcinoma cells.
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白介素6减少细胞细胞的缔合并增加导管乳腺癌细胞的运动。
DOI:
10.1084/jem.170.5.1649
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发表时间:
1989-11-01
影响因子:
15.3
通讯作者:
SEHGAL, PB
中科院分区:
文献类型:
--
作者:
TAMM, I;CARDINALE, I;KRUEGER, J;MURPHY, JS;MAY, LT;SEHGAL, PB
Treatment of transformed breast duct epithelial cells with IL-6 produces a unique cellular phenotype characterized by diminished proliferation and increased motility. Human ductal carcinoma cells (T- 47D and ZR-75-1 lines) are typically epithelioid in shape and form compact colonies in culture. Time-lapse cinemicrography shows that some untreated cells can transiently become fusiform or stellate in shape and separate from each other within a colony, but they usually rejoin their neighbors. While IL-6 suppresses the proliferation of these carcinoma cells, the IL-6-treated cells generally become stellate or fusiform and show increased motility. These changes persist as long as the cells are exposed to IL-6. This results in the dispersal of cells within colonies. The effects on cell growth, shape, and motility are reversible upon removal of IL-6. IL-6-treated T-47D cells display diminished adherens-type cell junctions, as indicated by markedly decreased vinculin-containing adhesions and intercellular desmosomal attachments. The effects on ZR-75-1 cell shape, colony number, and DNA synthesis are dependent on IL-6 concentration in the range from 0.15 to 15 ng/ml. Higher concentrations are required in T-47D cells for equivalent effects. Anti-IL-6 immune serum blocks IL-6 action. IL-6 represents a well-characterized molecule that regulates both the proliferation and junction-forming ability of breast ductal carcinoma cells.
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DOI:
10.1083/jcb.102.5.1843
发表时间:
1986-05
期刊:
The Journal of cell biology
影响因子:
--
作者:
Drenckhahn D;Franz H
通讯作者:
Franz H
DOI:
10.1073/pnas.83.10.3302
发表时间:
1986-05-01
影响因子:
11.1
作者:
LIOTTA, LA;MANDLER, R;SCHIFFMANN, E
通讯作者:
SCHIFFMANN, E
影响因子:
64.8
作者:
HIRANO, T;YASUKAWA, K;KISHIMOTO, T
通讯作者:
KISHIMOTO, T
DOI:
10.1016/s0006-291x(88)80043-3
发表时间:
1988-11-30
影响因子:
3.1
作者:
GANAPATHI, MK;MAY, LT;KUSHNER, I
通讯作者:
KUSHNER, I
影响因子:
7.8
作者:
PASDAR, M;NELSON, WJ
通讯作者:
NELSON, WJ