Masui T, Fukushima S, Katoh F, Yamasaki H, Ito N
First Department of Pathology, Nagoya City University Medical School, Japan.
Carcinogenesis. 1988 Jul;9(7):1143-6. doi: 10.1093/carcin/9.7.1143.
To study the mechanism of tumor promotion by different classes of urinary bladder promoters, the effect of sodium L-ascorbate, uracil and butylated hydroxyanisole (BHA) on junctional intercellular communication was examined in cultured BALB/c 3T3 cells using a dye-transfer method. In addition, since administration of sodium L-ascorbate and several other bladder tumor promoters is known to result in increased urinary pH, the effect of pH of the culture medium on intercellular communication was investigated. Results showed that under the present experimental conditions on the BALB/c 3T3 cells, BHA inhibited intercellular communication while sodium L-ascorbate and uracil did not. Intercellular communication was inhibited in proportion to the increase of medium pH after incubation of 4 h. Although further study is necessary to confirm the negative results of sodium L-ascorbate and uracil, these results suggest differences in the promoting mechanism(s) among these agents.
为研究不同种类膀胱促癌剂的促癌机制,采用染料转移法检测了L-抗坏血酸钠、尿嘧啶和丁基羟基茴香醚(BHA)对培养的BALB/c 3T3细胞间连接通讯的影响。此外,由于已知给予L-抗坏血酸钠和其他几种膀胱肿瘤促癌剂会导致尿液pH值升高,因此研究了培养基pH值对细胞间通讯的影响。结果表明,在目前针对BALB/c 3T3细胞的实验条件下,BHA抑制细胞间通讯,而L-抗坏血酸钠和尿嘧啶则无此作用。孵育4小时后,细胞间通讯随培养基pH值的升高而受到抑制。尽管需要进一步研究来证实L-抗坏血酸钠和尿嘧啶的阴性结果,但这些结果表明这些试剂在促癌机制上存在差异。