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Serum Requirement for in vitro Invasion by Tumor Cells

机译:肿瘤细胞对体外侵袭的血清需求

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摘要

The effect of fetal calf serum (FCS) on in vitro invasion by rat ascites hepatoma cells (AH130) was studied by using the in vitro invasion assay. Although the coculture of the highly invasive clone (MM1) of AH130 cells and the mesothelial cell layer or endothelial cell layer in modified minimum essential medium supplemented with 10% PCS resulted in extensive penetration of the layer by the tumor cells, the omission of PCS resulted in an almost complete elimination of the in vitro invasion. The in vitro invasiveness by human small cell lung cancer cells (OCIO) was also remarkably reduced by the omission of PCS from the assay medium, suggesting a requirement of serum for the in vitro tumor cell invasion. When 10% PCS was added to the medium 2 h after the tumor cell seeding in FCS‐free invasion assay system, penetration by MM1 cells was observed within an hour. This rate of penetration was almost the same as that when 10% PCS was added at the time of tumor cell seeding. PCS was also required for the penetration of a mesothelial cell monolayer by MM1 cells in a defined growth medium (SFM‐101), in which MM1 cells were well maintained. The invasion‐inducing activity appears to be independent of the growth‐stimulating activity in serum.
机译:利用体外侵袭试验研究了胎牛血清(FCS)对大鼠腹水肝癌细胞(AH130)体外侵袭的影响。尽管AH130细胞的高侵袭性克隆(MM1)与间皮细胞层或内皮细胞层在补充有10%PCS的改良的基本必需培养基中共培养导致肿瘤细胞对该层的广泛渗透,但PCS的缺失导致几乎完全消除了体外侵袭。由于从测定培养基中省略了PCS,还显着降低了人小细胞肺癌细胞(OCIO)的体外侵袭性,这表明体外肿瘤细胞侵袭需要血清。当在无FCS侵袭分析系统中接种肿瘤细胞后2小时,向培养基中添加10%PCS时,在一小时内观察到MM1细胞的渗透。该渗透率几乎与肿瘤细胞接种时添加10%PCS时的渗透率相同。 MM1细胞在定义良好的生长培养基(SFM-101)中穿透间皮细胞单层也需要PCS,在该培养基中MM1细胞保持良好。入侵诱导活性似乎与血清中的刺激生长活性无关。

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