Research Center, Dongnam Institute of Radiological & Medical Sciences, Busan 619-953, Republic of Korea.
Biochem Biophys Res Commun. 2013 Jan 25;430(4):1329-33. doi: 10.1016/j.bbrc.2012.10.119. Epub 2012 Dec 19.
Cancer stem cells (CSCs) are one of the main reasons behind cancer recurrence due to their resistance to conventional anti-cancer therapies. Thus, many efforts are being devoted to developing CSC-targeted therapies to overcome the resistance of CSCs to conventional anti-cancer therapies and decrease cancer recurrence. Differentiation therapy is one potential approach to achieve CSC-targeted therapies. This method involves inducing immature cancer cells with stem cell characteristics into more mature or differentiated cancer cells. In this study, we found that a CDK4 inhibitor sensitized MDA-MB-231 cells but not MCF7 cells to irradiation. This difference appeared to be associated with the relative percentage of CSC-population between the two breast cancer cells. The CDK4 inhibitor induced differentiation and reduced the cancer stem cell activity of MDA-MB-231 cells, which are shown by multiple marker or phenotypes of CSCs. Thus, these results suggest that radiosensitization effects may be caused by reducing the CSC-population of MDA-MB-231 through the use of the CDK4 inhibitor. Thus, further investigations into the possible application of the CDK4 inhibitor for CSC-targeted therapy should be performed to enhance the efficacy of radiotherapy for breast cancer.
癌症干细胞(CSCs)是癌症复发的主要原因之一,因为它们对常规抗癌疗法具有抵抗力。因此,许多人致力于开发针对 CSC 的治疗方法,以克服 CSCs 对常规抗癌疗法的耐药性并降低癌症复发率。分化疗法是实现 CSC 靶向治疗的一种潜在方法。该方法涉及诱导具有干细胞特征的未成熟癌细胞向更成熟或分化的癌细胞分化。在这项研究中,我们发现 CDK4 抑制剂可使 MDA-MB-231 细胞对辐射敏感,但对 MCF7 细胞则不然。这种差异似乎与两种乳腺癌细胞之间的 CSC 群体的相对百分比有关。CDK4 抑制剂诱导分化并降低了 MDA-MB-231 细胞的癌症干细胞活性,这可以通过 CSC 的多个标志物或表型来证明。因此,这些结果表明,放射增敏作用可能是通过使用 CDK4 抑制剂减少 MDA-MB-231 中的 CSC 群体而引起的。因此,应进一步研究 CDK4 抑制剂在 CSC 靶向治疗中的可能应用,以提高乳腺癌放疗的疗效。