Department of Surgery, Institute of Health Biosciences, The University of Tokushima, Tokushima, Japan.
Department of Surgery, Institute of Health Biosciences, The University of Tokushima, Tokushima, Japan
Anticancer Res. 2014 Sep;34(9):4709-16.
BACKGROUND/AIM: Recent studies have demonstrated the efficacy of irradiation from light emitting diodes (LED) for wound healing, anti-inflammation and anticancer therapies. However, little is known about the effects of visible light in colon cancer cells. The purpose of this study was to evaluate the biological response (including gene expression changes) of human colon cancer cells to different wavelengths of LED irradiation.
Human colon cancer cells (HT29 or HCT116) were seeded onto laboratory dishes that were then put on LED irradiation equipment with a 465 nm-, 525 nm-, or 635 nm-LED. Irradiation at 15 or 30 mW was performed 10 min/day, each day for 5 days. The cell counting kit8 was then used to measure cell viability. Apoptosis and expression of several mRNAs (caspase, MAPK and autophagy pathway) in HT29 cultures irradiated with 465 nm LED were evaluated via AnnexinV/PI and RT-PCR, respectively.
Viability of HT29 and HCT116 cells was lower in 465 nm-LED irradiated cultures than in control cultures, but viability of HT29 cells did not differ between control cultures and 525 nm-LED or 635 nm-LED irradiated cultures. Moreover, the expression of FAS, caspase-3, capase-8, and JUK were significantly higher in 465 nm-LED irradiated cultures than in control cultures, and expression of ERK1/2 and LC3 was lower in blue-irradiated cells.
LED irradiation at 465 nm inhibited the proliferation of HT29 cells and of HCT116 cells. Notably, LED irradiation at 465 nm promoted apoptosis inHT29 cultures via the extrinsic apoptosis pathway and the MAPK pathway.
背景/目的:最近的研究表明,发光二极管(LED)的光照射在伤口愈合、抗炎和抗癌治疗方面是有效的。然而,对于可见光在结肠癌细胞中的作用知之甚少。本研究旨在评估不同波长的 LED 照射对人结肠癌细胞的生物学反应(包括基因表达变化)。
将人结肠癌细胞(HT29 或 HCT116)接种在培养皿上,然后将培养皿放在具有 465nm、525nm 或 635nm-LED 的 LED 照射设备上。每天照射 10 分钟,每天 15 或 30mW。然后使用细胞计数试剂盒 8 测量细胞活力。通过 AnnexinV/PI 和 RT-PCR 分别评估用 465nm-LED 照射的 HT29 培养物中的细胞凋亡和几种 mRNA(caspase、MAPK 和自噬途径)的表达。
与对照组相比,465nm-LED 照射的 HT29 和 HCT116 细胞活力较低,但 HT29 细胞的活力在对照组与 525nm-LED 或 635nm-LED 照射的培养物之间没有差异。此外,465nm-LED 照射培养物中 FAS、caspase-3、caspase-8 和 JUK 的表达明显高于对照组,而 ERK1/2 和 LC3 的表达在蓝光照射细胞中较低。
465nm-LED 照射抑制了 HT29 细胞和 HCT116 细胞的增殖。值得注意的是,465nm-LED 照射通过外源性凋亡途径和 MAPK 途径促进 HT29 培养物中的细胞凋亡。