Zhang J, Fang W, Zheng J
Department of Pathology, Beijing Medical University.
Zhonghua Bing Li Xue Za Zhi. 1997 Feb;26(1):16-8.
To study the effects of two cAMP analogs with different site-selectivity on growth and differentiation of metastatic human lung cancer cells.
The methods used include cell culture, in vitro invasion assay, soft agar colony formation assay, immunocytochemistry and electron microscopy. A metastatic human lung cancer cell line gwas treated with dibutyryl cAMP (db-cAMP, non-site-selective) or 8-chloro-cAMP (8-Cl-cAMP, site-selective for type II PKA).
Treatment of PG cells with 1 mmol/L of db-cAMP for 7 days resulted in 48% growth inhibition, while treatment with 20 mumol/L of 8-Cl-cAMP gave 70% growth inhibition. The growth inhibitory effect of db-cAMP was shown to be reversible, while that of 8-Cl-cAMP was not. The ability of PG cells to penetrate matrigel-coated membrane and to form colonies in soft agar was also significantly inhibited by treatment with these two drugs. Microscopic observation showed that cells formed elongated cytoplasmic processes and increased expression of neuron-specific enolase as well as chromogranin after treatment.
The objective to inhibit malignancy could be reached by activation of specific PKA with site-selective cAMP analogs.
研究两种具有不同位点选择性的环磷酸腺苷(cAMP)类似物对人转移性肺癌细胞生长和分化的影响。
所采用的方法包括细胞培养、体外侵袭试验、软琼脂集落形成试验、免疫细胞化学和电子显微镜检查。用人转移性肺癌细胞系分别用二丁酰环磷腺苷(db - cAMP,非位点选择性)或8 - 氯环磷腺苷(8 - Cl - cAMP,对II型蛋白激酶A具有位点选择性)进行处理。
用1 mmol/L的db - cAMP处理PG细胞7天导致生长抑制48%,而用20 μmol/L的8 - Cl - cAMP处理则导致生长抑制70%。结果表明db - cAMP的生长抑制作用是可逆的,而8 - Cl - cAMP的则不可逆。用这两种药物处理也显著抑制了PG细胞穿透基质胶包被膜和在软琼脂中形成集落的能力。显微镜观察显示,处理后细胞形成伸长的细胞质突起,并增加了神经元特异性烯醇化酶和嗜铬粒蛋白的表达。
通过用位点选择性cAMP类似物激活特异性蛋白激酶A可达到抑制恶性肿瘤的目的。