Banoub R W, Fernstrom M, Ruch R J
Department of Pathology, Medical College of Ohio, Toledo 43614, USA.
Cancer Lett. 1996 Nov 12;108(1):35-40. doi: 10.1016/s0304-3835(96)04367-4.
The carotenoid, beta-carotene, has been examined in human trials as a possible lung cancer chemopreventive agent, but initial results indicate that the compound is ineffective. Here we have considered whether beta-carotene could enhance gap junctional intercellular communication (GJIC) and affect the growth of lung epithelial cells, since these effects may be involved in the carotenoid's chemopreventive actions. In accordance with its lack of lung cancer chemopreventive activity, beta-carotene (1-10 microM; 1-5 days treatment durations) did not affect GJIC, gap junction protein (connexin43; Cx43) expression, or growth in vitro of non-transformed (C10) or neoplastic (E9 and 82-132) murine lung epithelial cells. beta-Carotene enhanced GJIC and Cx43 expression and reduced the growth of C3H10T1/2 murine fibroblasts, however. These data indicate that the effects of beta-carotene on GJIC and growth are cell-specific which may partly explain why the carotenoid is an ineffective lung cancer chemopreventive agent.
类胡萝卜素β-胡萝卜素已在人体试验中作为一种可能的肺癌化学预防剂进行了研究,但初步结果表明该化合物无效。在此,我们探讨了β-胡萝卜素是否能够增强细胞间隙连接通讯(GJIC)并影响肺上皮细胞的生长,因为这些效应可能与类胡萝卜素的化学预防作用有关。鉴于其缺乏肺癌化学预防活性,β-胡萝卜素(1 - 10微摩尔;处理持续时间为1 - 5天)对未转化的(C10)或肿瘤性的(E9和82 - 132)小鼠肺上皮细胞的GJIC、间隙连接蛋白(连接蛋白43;Cx43)表达或体外生长均无影响。然而,β-胡萝卜素增强了C3H10T1/2小鼠成纤维细胞的GJIC和Cx43表达,并降低了其生长速度。这些数据表明,β-胡萝卜素对GJIC和生长的影响具有细胞特异性,这可能部分解释了为什么该类胡萝卜素是一种无效的肺癌化学预防剂。