Kee K A, Finan T M, Korman L Y, Moody T W
Department of Biochemistry, George Washington University School of Medicine and Health Sciences, Washington, DC 20037.
Peptides. 1988;9 Suppl 1:257-61. doi: 10.1016/0196-9781(88)90251-3.
The effects of somatostatin (SRIF) on small cell lung cancer (SCLC) cell line NCI-H345 was investigated. SRIF had no effects on the basal cAMP levels or the secretion rate of bombesin-like peptides. VIP (1 microM) increased the cAMP levels approximately 10-fold and the secretion rate of bombesin-like peptides 3-fold. SRIF and its analogues inhibited the increase in the cAMP levels and the secretion rate of bombesin-like peptides caused by VIP. The order of peptide potency was (D-Trp8)SRIF > SRIF-28 = (Tyr11)SRIF > SRIF. These data suggest that functional SRIF receptors may be present on SCLC cells.
研究了生长抑素(SRIF)对小细胞肺癌(SCLC)细胞系NCI-H345的影响。SRIF对基础环磷酸腺苷(cAMP)水平或蛙皮素样肽的分泌率无影响。血管活性肠肽(VIP,1微摩尔)使cAMP水平增加约10倍,蛙皮素样肽的分泌率增加3倍。SRIF及其类似物抑制了由VIP引起的cAMP水平升高和蛙皮素样肽的分泌率增加。肽的效力顺序为(D-色氨酸8)SRIF > SRIF-28 =(酪氨酸11)SRIF > SRIF。这些数据表明SCLC细胞上可能存在功能性SRIF受体。